hPSCreg®
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Search results

  1. AAKIPSi001-A

    France INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (AAKIPS)
    Disease:

    Aniridia

  2. AAKIPSi002-A

    France INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (AAKIPS)
    Disease:

    Aniridia

  3. AAKIPSi003-A

    France INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (AAKIPS)
    Disease:

    Aniridia

  4. ABi001-A

    Russia Moscow Institute of Physics and Technology (National Research University) (AB)
    Disease:

    Cone dystrophy with supernormal rod response

  5. ABi002-A

    Russia Moscow Institute of Physics and Technology (National Research University) (AB)
    Disease:

    Cone dystrophy with supernormal rod response

  6. ABi004-A (KAA)

    Russia Moscow Institute of Physics and Technology (National Research University) (AB)
    Disease:

    Cone dystrophy with supernormal rod response

  7. ABCRIi001-A (hiPSC_ALFAS037_C9)

    Portugal Algarve Biomedical Center Research Institute (ABC-Ri) (ABCRI)
    Disease:

    Normal (average)

  8. ABCRIi002-A (#4C1)

    Portugal Algarve Biomedical Center Research Institute (ABC-Ri) (ABCRI)
    Disease:

    Normal (average)

  9. ABCRIi003-A (#8C3)

    Portugal Algarve Biomedical Center Research Institute (ABC-Ri) (ABCRI)
    Disease:

    Complete trisomy 21 syndrome

  10. ABCRIi004-A (#12C2)

    Portugal Algarve Biomedical Center Research Institute (ABC-Ri) (ABCRI)
    Disease:

    Complete trisomy 21 syndrome

  11. ABCRIi005-A (#16C9)

    Portugal Algarve Biomedical Center Research Institute (ABC-Ri) (ABCRI)
    Disease:

    Normal (average)

  12. AHJNMUi001-A

    China Affiliated Hospital of Jining Medical University(AHJNMU) (AHJNMU)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  13. AHMUi001-A

    China dongmei ji (AHMU)
    Disease:

    Leber hereditary optic neuropathy

  14. AHMUi004-A (AHMUMTi004-1)

    China dongmei ji (AHMU)

  15. AHMUCNi002-A (ABCA7-KO-iPSC)

    China Anhui Medical University (AHMUCN)
    Disease:

    Normal (average)

  16. AHMUCNi004-A (AHMUCN-DS3L)

    China Anhui Medical University (AHMUCN)
    Disease:

    Down syndrome

  17. AHQUi001-A (IPS35-2)

    China Affiliated Hospital of Qingdao University (AHQU)
    Disease:

    Non rare in europe: hyperlipoproteinemia type 4

  18. AHQUi001-A-1 (IPS35-2-R)

    China Affiliated Hospital of Qingdao University (AHQU)
    Disease:

    Non rare in europe: hyperlipoproteinemia type 4

  19. AIBNi015-A (SPG1-AU01C15)

    Australia Australian Institute for Bioengineering and Nanotechnology (AIBN)
    Disease:

    Hereditary spastic paraplegia 56

  20. AIBNi016-A (SPG2-S376C1)

    Australia Australian Institute for Bioengineering and Nanotechnology (AIBN)
    Disease:

    Hereditary spastic paraplegia 56

  21. AIBNi017-A (SPGh1-S075mC2)

    Australia Australian Institute for Bioengineering and Nanotechnology (AIBN)
    Disease:

    Hereditary spastic paraplegia 56

  22. AIBNi018-A (SPGh2-S964pC6)

    Australia Australian Institute for Bioengineering and Nanotechnology (AIBN)
    Disease:

    Hereditary spastic paraplegia 56

  23. AIBNi019-A (AB-001-300924-MT)

    Australia Australian Institute for Bioengineering and Nanotechnology (AIBN)
    Disease:

    Phenylketonuria

  24. AIBNi020-A (CN-002-300924-MT)

    Australia Australian Institute for Bioengineering and Nanotechnology (AIBN)
    Disease:

    Phenylketonuria

  25. AIBNi021-A (PM-003-300924-SB)

    Australia Australian Institute for Bioengineering and Nanotechnology (AIBN)
    Disease:

    Phenylketonuria

  26. AIBNi022-A (JR-004-300924-SB)

    Australia Australian Institute for Bioengineering and Nanotechnology (AIBN)
    Disease:

    Phenylketonuria

  27. AIBNi023-A (AIBNCASK01)

    Australia Australian Institute for Bioengineering and Nanotechnology (AIBN)
    Disease:

    Cask-related intellectual disability

  28. AIBNi024-A (AIBNCASK02)

    Australia Australian Institute for Bioengineering and Nanotechnology (AIBN)
    Disease:

    Cask-related intellectual disability

  29. UCSFi001-A-1 (AICS-0005-050)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  30. UCSFi001-A-2 (AICS-0012-105)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  31. UCSFi001-A-3 (AICS-0016-184)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  32. UCSFi001-A-4 (AICS-0075-085)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  33. UCSFi001-A-5 (AICS-0011-027)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  34. UCSFi001-A-6 (AICS-0013-210)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  35. UCSFi001-A-7 (AICS-0017-065)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  36. UCSFi001-A-8 (AICS-0010-055)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  37. UCSFi001-A-9 (AICS-0014-006)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  38. UCSFi001-A-10 (AICS-0023-020)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  39. UCSFi001-A-11 (AICS-0024-080)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  40. UCSFi001-A-12 (AICS-0036-006)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  41. UCSFi001-A-13 (AICS-0022-037)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  42. UCSFi001-A-14 (AICS-0025-001)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  43. UCSFi001-A-15 (AICS-0025-044)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  44. UCSFi001-A-16 (AICS-0031-035)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  45. UCSFi001-A-17 (AICS-0032-019)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  46. UCSFi001-A-18 (AICS-0030-022)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  47. UCSFi001-A-19 (AICS-0033-115)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  48. UCSFi001-A-20 (AICS-0040-013)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  49. UCSFi001-A-21 (AICS-0040-035)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  50. UCSFi001-A-22 (AICS-0053-016)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  51. UCSFi001-A-23 (AICS-0054-091)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  52. UCSFi001-A-24 (AICS-0057-050)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  53. UCSFi001-A-25 (AICS-0058-067)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  54. UCSFi001-A-26 (AICS-0037-172)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  55. UCSFi001-A-27 (AICS-0048-039)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  56. UCSFi001-A-28 (AICS-0061-036)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  57. UCSFi001-A-29 (AICS-0052-003)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  58. UCSFi001-A-30 (AICS-0046-051)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  59. UCSFi001-A-31 (AICS-0069-088)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  60. UCSFi001-A-32 (AICS-0060-027)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  61. UCSFi001-A-33 (AICS-0059-036)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  62. UCSFi001-A-34 (AICS-0068-009)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  63. UCSFi001-A-35 (AICS-0080-069)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  64. UCSFi001-A-36 (AICS-0036-028)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  65. UCSFi001-A-37 (AICS-0074-026)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  66. UCSFi001-A-38 (AICS-0084-018)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  67. UCSFi001-A-39 (AICS-089-061)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  68. UCSFi001-A-40 (AICS-094-024)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  69. UCSFi001-A-41 (AICS-0034-062)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  70. UCSFi001-A-42 (AICS-0086-147)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  71. UCSFi001-A-43 (AICS-0087-031)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  72. UCSFi001-A-44 (AICS-0063-096)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  73. UCSFi001-A-45 (AICS-0090-391)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  74. UCSFi001-A-46 (AICS-0095-018)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  75. UCSFi001-A-47 (AICS-0096-074)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  76. UCSFi001-A-48 (AICS-0093-025)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  77. UCSFi001-A-55 (AICS-0078-079)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  78. UCSFi001-A-56 (AICS-0088-083)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  79. UCSFi001-A-57 (AICS-0099-020)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  80. UCSFi001-A-63 (AICS-0082-001)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  81. UCSFi001-A-66 (AICS-0114-032)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  82. UCSFi001-A-67 (AICS-0114-035)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  83. UCSFi001-A-69 (AICS-0083-005)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  84. UCSFi001-A-70 (AICS-0083-124)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  85. UCSFi001-A-89 (AICS-0097-102)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  86. UCSFi001-A-90 (AICS-0097-141)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  87. UCSFi001-A-91 (AICS-0097-157)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  88. UCSFi001-A-92 (AICS-0097-113)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  89. UCSFi001-A-93 (AICS-0097-174)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  90. UCSFi001-A-94 (AICS-0104-003)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  91. UCSFi001-A-95 (AICS-0104-085)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  92. UCSFi001-A-96 (AICS-0104-004)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  93. UCSFi001-A-97 (AICS-0104-006)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  94. UCSFi001-A-98 (AICS-0105-022)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  95. UCSFi001-A-99 (AICS-0105-030)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  96. UCSFi001-A-A (AICS-0105-031)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  97. UCSFi001-A-B (AICS-0105-032)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  98. UCSFi001-A-C (AICS-0105-057)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  99. UCSFi001-A-D (AICS-0105-089)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  100. UCSFi001-A-E (AICS-0106-040)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  101. UCSFi001-A-F (AICS-0106-088)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  102. UCSFi001-A-G (AICS-0106-104)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  103. UCSFi001-A-H (AICS-0106-134)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  104. UCSFi001-A-I (AICS-0107-009)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  105. UCSFi001-A-J (AICS-0107-017)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  106. UCSFi001-A-K (AICS-0107-063)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  107. UCSFi001-A-L (AICS-0109-055)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  108. UCSFi001-A-M (AICS-0109-056)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  109. UCSFi001-A-N (AICS-0109-072)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  110. UCSFi001-A-O (AICS-0109-093)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Cardiomyopathy

  111. UCSFi001-A-P (AICS-0113-002)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Skeletal myopathy

  112. UCSFi001-A-Q (AICS-0113-023)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  113. UCSFi001-A-R (AICS-0113-030)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Skeletal myopathy

  114. UCSFi001-A-S (AICS-0113-044)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  115. UCSFi001-A-T (AICS-0113-057)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  116. UCSFi001-A-U (AICS-0113-082)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Skeletal myopathy

  117. UCSFi001-A-V (AICS-0119-010)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Laminopathy

  118. UCSFi001-A-W (AICS-0119-023)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  119. UCSFi001-A-X (AICS-0119-039)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Laminopathy

  120. UCSFi001-A-Y (AICS-0119-045)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  121. UCSFi001-A-1D (AICS-0120-204)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  122. UCSFi001-A-1E (AICS-0102-330)

    United States Allen Institute for Cell Science (AICS)
    Disease:

    Normal (average)

  123. AMUFAHi001-A

    China The First Affiliated Hospital of Anhui Medical University (AMUFAH)
    Disease:

    Normal (average)

  124. AMUFAHi002-A (AY20210813)

    China The First Affiliated Hospital of Anhui Medical University (AMUFAH)
    Disease:

    Obsolete_polycystic ovary syndrome

  125. AMUFAHi003-A

    China The First Affiliated Hospital of Anhui Medical University (AMUFAH)
    Disease:

    Normal (average)

  126. RUCDRi002-A-72

    Austria Angios GmbH (ANGIOS)
    Disease:

    Normal (average)

  127. AOUMEYi002-A

    Italy Meyer Children's Hospital IRCCS (AOUMEY)
    Disease:

    Gm3 synthase deficiency

  128. AOUMEYi003-A

    Italy Meyer Children's Hospital IRCCS (AOUMEY)
    Disease:

    Morquio syndrome

  129. ASGRCi001-A (F3-2#5 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Normal (average)

  130. ASGRCi002-A (F3-3#1 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

  131. ASGRCi003-A (F3-4#5 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

  132. ASGRCi004-A (0118 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Obsolete_proliferative diabetic retinopathy

    Disease:

    Type 2 diabetes mellitus

  133. ASGRCi005-A (0622 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Keratoconjunctivitis sicca

  134. ASGRCi006-A (0808 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Obsolete_proliferative diabetic retinopathy

  135. ASGRCi007-A (T2D19#2 XY-CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

  136. ATCi002-A

    China Aegicare (Shenzhen) Technology Co (ATC)
    Disease:

    Keipert syndrome

  137. ATLABi001-A (AT-MODY3-iP001)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Hepatocyte nuclear factor 1-alpha-associated monogenic diabetes

  138. ATLABi002-A (AT-MODY3-iP002)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Hepatocyte nuclear factor 1-alpha-associated monogenic diabetes

  139. ATLABi003-A (AT-Normal-i70)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Normal (average)

  140. ATLABi004-A (AT-Normal-i173)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Normal (average)

  141. ATLABi005-A (AT-Normal-i104)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Normal (average)

  142. ATLABi006-A (AT-UC C Normal-iC16)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Normal (average)

  143. ATLABi007-A (AT-UC C Normal-iC46)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Normal (average)

  144. ATLABi008-A (AT-UC I Normal-iC06)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Normal (average)

  145. ATLABi009-A (AT-UC I Normal-iC13)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Normal (average)

  146. ATLABi010-A (AT-MODY10-iII1)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Maturity-onset diabetes of the young type 10

  147. ATLABi011-A (AT-MODY10-iII4)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Maturity-onset diabetes of the young type 10

  148. ATLABi012-A (AT-M10 Normal-iI2)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Normal (average)

  149. ATLABi013-A (AT-M10 Normal-iII3)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Normal (average)

  150. ATLABi014-A (AT-MODY10-iI1)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Maturity-onset diabetes of the young type 10

  151. ATLABi015-A (AT-Diabetic-i131)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Diabetes mellitus

  152. ATLABi016-A (AT-Diabetic-i107)

    Singapore IMCB, Adrian Teo's Lab (ATLAB)
    Disease:

    Diabetes mellitus

  153. AUi001-A

    Denmark Aarhus University (AU)
    Disease:

    Herpes simplex encephalitis

  154. AUMCi001-A (LUMC0195iFOXC)

    Netherlands Amsterdam University Medical Centers (AUMC)

  155. AUMCi001-A-1

    Netherlands Amsterdam University Medical Centers (AUMC)

  156. AUMCi002-A (LUMC0203iOCA)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Oculocutaneous albinism type 1a

  157. AUMCi003-A (LUMC0147iXLRS)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    X-linked retinoschisis

  158. AUMCi004-A (LUMC0181iXLRS)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    X-linked retinoschisis

  159. AUMCi005-A (LUMC0182iXLRS)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    X-linked retinoschisis

  160. AUMCi006-A (LUMC0196iOAT)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Gyrate atrophy of choroid and retina

  161. AUMCi007-A (LUMC0204iOAT)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Gyrate atrophy of choroid and retina

  162. AUMCi008-A (LUMC0296iOAT)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Gyrate atrophy of choroid and retina

  163. AUMCi009-A (LUMC0251iSLC)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome

  164. AUMCi010-A (LF2A_C02 and LUMC0255iHCM02)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  165. AUMCi010-B (LUMC0255iHCM03 and LF2A_C03)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  166. AUMCi010-C (LF2A_C04 and LUMC0255iHCM04)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  167. AUMCi010-D (LF2A_C01 and LUMC0255iHCM01)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  168. AUMCi010-E (LF2A_C05 and LUMC0255iHCM05)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  169. AUMCi010-F (LUMC0255iHCM06 and LF2A_C06)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  170. AUMCi011-A (LF2B_C01 and LUMC0258iHCM01)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  171. AUMCi011-B (LUMC0258iHCM04 and LF2B_C04)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  172. AUMCi011-C (LUMC0258iHCM05 and LF2B_C05)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  173. AUMCi011-D (LUMC0258iHCM02 and LF2B_C02)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  174. AUMCi011-E (LUMC0258iHCM03 and LF2B_C03)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  175. AUMCi011-F (LUMC0258iHCM06 and LF2B_C06)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  176. AUMCi012-A (LUMC0281iHCM10 and LF3A_C10)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  177. AUMCi012-B (LF3A_C14 and LUMC0281iHCM14)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  178. AUMCi012-C (LF3A_C15 and LUMC0281iHCM15)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  179. AUMCi012-D (LF3A_C01 and LUMC0281iHCM01)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  180. AUMCi012-E (LF3A_C03 and LUMC0281iHCM03)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  181. AUMCi012-F (LUMC0281iHCM06 and LF3A_C06)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  182. AUMCi013-A (LUMC0282iHCM02 and LF3B_C02)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  183. AUMCi013-B (LF3B_C04 and LUMC0282iHCM04)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  184. AUMCi013-C (LF3B_C05 and LUMC0282iHCM05)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  185. AUMCi013-D (LF3B_C03 and LUMC0282iHCM03)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  186. AUMCi013-E (LF3B_C09 and LUMC0282iHCM09)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  187. AUMCi013-F (LF3B_C14 and LUMC0282iHCM14)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  188. AUMCi014-A (LF3C_C02 and LUMC0283iHCM02)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  189. AUMCi014-B (LF3C_C05 and LUMC0283iHCM05)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  190. AUMCi014-C (LF3C_C07 and LUMC0283iHCM07)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  191. AUMCi014-D (LF3C_C01 and LUMC0283iHCM01)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  192. AUMCi014-E (LF3C_C03 and LUMC0283iHCM03)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  193. AUMCi014-F (LUMC0283iHCM06 and LF3C_C06)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  194. AUMCi014-G (LF3C_C09 and LUMC0283iHCM09)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  195. AUMCi014-H (MF3C_C08)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  196. AUMCi014-I (MF3C_C20)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  197. AUMCi014-J (MF3C_C31)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  198. AUMCi015-A (LMNA-D44)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Dilated cardiomyopathy

  199. AUMCi015-A-1 (LMNA-D44-PE1-A43B)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Dilated cardiomyopathy

  200. AUMCi016-A (LUMC0277iFBN01)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Marfan syndrome

  201. AUMCi017-A (LUMC0278iFBN04)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Marfan syndrome

  202. AUMCi018-A (LUMC0279iFBN02)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Marfan syndrome

  203. AUSCIi001-A

    Turkey Ankara University Stem Cell Institute (AUSCI)
    Disease:

    Spinal muscular atrophy

  204. BAFYi001-A

    China Shenzhen Baoan Women's and Children's Hospital (BAFY)
    Disease:

    Edwards syndrome

  205. BBANTWi001-A (iPSC_FB_M45-50_C9)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  206. BBANTWi001-B (iPSC_FB_M45-50_C15)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  207. BBANTWi001-C (iPSC_FB_M45-50_C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  208. BBANTWi006-A (iPSC_BrS9_FB_C7)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome 1

  209. BBANTWi007-A (iPSC_BrS10_FB_C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome 1

  210. BBANTWi008-A (iPSC_PBMC_LDS_SMAD3_T1_C11)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 3

  211. BBANTWi009-A

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Meester-loeys syndrome

  212. BBANTWi010-A (iPSC_PBMC_LDS_TGFB3_KE2M_C9)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 5

  213. BBANTWi011-A

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Familial thoracic aortic aneurysm and aortic dissection

  214. BBANTWi012-A (F1990.01 C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  215. BBANTWi012-A-1 (TTN_E48_V4623*)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

  216. BBANTWi012-A-2 (iPSC_FB_F19901C3_TTN_E48_L4612*)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

  217. BBANTWi012-A-3 (iPSC_FB_F19901C3_TTN_E357_E33459*_N33456N_C30)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

  218. BBANTWi012-A-4 (iPSC_FB_F19901C3_TTN_E357_V33467*_N33456N_C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

  219. BBANTWi012-A-5 (iPSC_F199001_C3_CRISPR_CACNA1C_T330M_HMZ_C6)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome

  220. BBANTWi012-A-6 (iPSC_F199001_C3_CRISPR_CACNA1C_T330M_HTZ_C11.2)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome

  221. BBSSPAi001-A (Ctrl FiPS1-Sv4F-25)

    Spain Biobanco del Sistema Sanitario Público de Andalucía (BBSSPA)
    Disease:

    Normal (average)

  222. BBSSPAi002-A (AD-PBiPS1-Sv4F-1)

    Spain Biobanco del Sistema Sanitario Público de Andalucía (BBSSPA)
    Disease:

    Alzheimer's disease

  223. BCHi007-A (HNDS0005-01 #B)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  224. BCHi007-A-1 (HNDS0005-01 #B2 +/+)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  225. BCHi009-A (HNDS0002-01 #D)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  226. BCHi009-A-1 (HNDS0002-01 #D CC26 +/+)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  227. BCHi011-A (HNDS0003-01 #F)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  228. BCHi011-A-1 (HNDS0003-01 #F CC39 +/+)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  229. BCHi013-A (HNDS0143-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  230. BCHi013-A-1 (HNDS0143-01#A CNC21(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  231. BCHi013-A-2 (HNDS0143-01#A CNC24(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  232. BCHi013-A-3 (HNDS0143-01#A CC12(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  233. BCHi013-A-4 (HNDS0143-01#A CC28(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  234. BCHi014-A (HNDS141-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  235. BCHi014-A-1 (HNDS0141-01#B CNC22(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  236. BCHi014-A-2 (HNDS0141-01#B CNC35(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  237. BCHi014-A-3 (HNDS0141-01#B CC6(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  238. BCHi014-A-4 (HNDS0141-01#B CC43(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  239. BCHi014-A-5 (HNDS0141-01#B CC8(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  240. BCHi014-A-6 (HNDS0141-01#B CC23(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  241. BCHi014-A-7 (HNDS0141-01#B KO7(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  242. BCHi014-A-8 (HNDS0141-01#B KO14(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  243. BCHi015-A (HNDS0138-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  244. BCHi015-A-1 (HNDS0138-01#B CNC24(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  245. BCHi015-A-2 (HNDS0138-01#B CNC42(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  246. BCHi015-A-3 (HNDS0138-01#B CC38(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  247. BCHi015-A-4 (HNDS0138-01#B CC51(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  248. BCHi015-A-5 (HNDS0138-01#B CC6(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  249. BCHi015-A-6 (HNDS0138-01#B CC11(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  250. BCHi016-A (HNDS0151-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  251. BCHi016-A-1 (HNDS0151-01#B CNC20(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  252. BCHi016-A-2 (HNDS0151-01#B CNC43(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  253. BCHi016-A-3 (HNDS0151-01#B CC18(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  254. BCHi016-A-4 (HNDS0151-01#B CC23(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  255. BCHi017-A (HNDS0164-01#D)

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  256. BCHi017-A-1 (HNDS0164-01#D CNC9(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  257. BCHi017-A-2 (HNDS0164-01#D CNC11(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  258. BCHi017-A-3 (HNDS0164-01#D CC2(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  259. BCHi017-A-4 (HNDS0164-01#D CC16(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  260. BCHi017-A-5 (HNDS0164-01#D CC3(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  261. BCHi017-A-6 (HNDS0164-01#D CC10(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  262. BCHi018-A (HNDS0176-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  263. BCHi018-A-1 (HNDS0176-01#A CNC10(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  264. BCHi018-A-2 (HNDS0176-01#A CNC35(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  265. BCHi018-A-3 (HNDS0176-01#A CC3(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  266. BCHi018-A-4 (HNDS0176-01#A CC16(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  267. BCHi018-A-5 (HNDS0176-01#A CC38(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  268. BCHi018-A-6 (HNDS0176-01#A CC48(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  269. BCHi019-A (HNDS0179-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  270. BCHi019-A-1 (HNDS0179-01#B CNC2(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  271. BCHi019-A-2 (HNDS0179-01#B CNC21(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  272. BCHi019-A-3 (HNDS0179-01#B CC13(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  273. BCHi019-A-4 (HNDS0179-01#B CC15(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  274. BCHi019-A-5 (HNDS0179-01#B CC26(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  275. BCHi019-A-7 (HNDS0179-01#B KO32(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  276. BCHi020-A (HNDS0163-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  277. BCHi020-A-1 (HNDS0163-01#B CNC20(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  278. BCHi020-A-2 (HNDS0163-01#B CC19(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  279. BCHi020-A-3 (HNDS0163-01#B CC34(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  280. BCHi020-A-4 (HNDS0163-01#B CC12(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  281. BCHi021-A (HNDS0129-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  282. BCHi021-A-1 (HNDS0129-01#A CNC7(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  283. BCHi021-A-2 (HNDS0129-01#A CC20(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  284. BCHi021-A-3 (HNDS0129-01#A CC47(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  285. BCHi021-A-4 (HNDS0129-01#A CNC8(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  286. BCHi021-A-5 (HNDS0129-01#A CC28(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  287. BCHi021-A-6 (HNDS0129-01#A CC55(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  288. BCHi022-A (HNDS0108-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  289. BCHi022-A-1 (HNDS0108-01#B CNC7(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  290. BCHi022-A-2 (HNDS0108-01#B CC5(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  291. BCHi022-A-3 (HNDS0108-01#B CNC36(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  292. BCHi022-A-4 (HNDS0108-01#B CC20(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  293. BCHi023-A (HNDS0105-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  294. BCHi023-A-1 (HNDS0105-01#B CNC5(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  295. BCHi023-A-2 (HNDS0105-01#B CC28(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  296. BCHi023-A-3 (HNDS0105-01#B CNC19(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  297. BCHi023-A-4 (HNDS0105-01#B CC42(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  298. BCHi024-A (HNDS0142-01#D)

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  299. BCHi024-A-1 (HNDS0142-01#D CNC11(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  300. BCHi024-A-2 (HNDS0142-01#D CC45-6(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  301. BCHi024-A-3 (HNDS0142-01#D CNC23(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  302. BCHi024-A-4 (HNDS0142-01#D CC16(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  303. BCHi025-A (HNDS0140-01#C)

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  304. BCHi025-A-1 (HNDS0140-01#C CNC30(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  305. BCHi025-A-2 (HNDS0140-01#C CC8(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  306. BCHi025-A-3 (HNDS0140-01#C CNC37(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  307. BCHi025-A-4 (HNDS0140-01#C CC16(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  308. BCHi026-A (HNDS0136-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  309. BCHi026-A-1 (HNDS0136-01#A CNC1(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  310. BCHi026-A-2 (HNDS0136-01#A CC20(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  311. BCHi026-A-3 (HNDS0136-01#A CNC19(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  312. BCHi026-A-4 (HNDS0136-01#A CC23(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  313. BCHi027-A (HNDS0145-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  314. BCHi027-A-1 (HNDS0145-01#A CNC17(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  315. BCHi027-A-2 (HNDS0145-01#A CC32-1(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  316. BCHi027-A-3 (HNDS0145-01#A CC3(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  317. BCHi027-A-4 (HNDS0145-01#A CNC21(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  318. BCHi027-A-5 (HNDS0145-01#A CC32-24(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  319. BCHi027-A-6 (HNDS0145-01#A CC9(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  320. BCHi028-A (HNDS0171-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  321. BCHi028-A-1 (HNDS0171-01#A CNC2(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  322. BCHi028-A-2 (HNDS0171-01#A CC10(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  323. BCHi028-A-3 (HNDS0171-01#A CNC12(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  324. BCHi028-A-4 (HNDS0171-01#A CC16(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  325. BCHi029-A (HNDS0121-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  326. BCHi029-B (HNDS0121-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  327. BCHi030-A (HNDS0131-01#H)

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  328. BCHi030-B (HNDS0131-01#I)

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  329. BCHi031-A (HNDS0032-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  330. BCHi031-A-1 (HNDS0032-01#A CNC6(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  331. BCHi031-A-2 (HNDS0032-01#A CNC20(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  332. BCHi031-A-3 (HNDS0032-01#A CC10(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  333. BCHi031-A-4 (HNDS0032-01#A CC31(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  334. BCHi032-A (HNDS0038-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  335. BCHi032-A-1 (HNDS0038-01#A Pass-Match-Control)

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  336. BCHi032-A-2 (HNDS0038-01#A CC19(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  337. BCHi032-A-3 (HNDS0038-01#A CC29(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  338. BCHi033-A (HNDS0060-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  339. BCHi033-A-1 (HNDS0060-01#B CNC18(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  340. BCHi033-A-2 (HNDS0060-01#B CNC22(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  341. BCHi033-A-3 (HNDS0060-01#B CC9(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  342. BCHi033-A-4 (HNDS0060-01#B CC21(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  343. BCHi034-A (HNDS0181-01#F)

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  344. BCHi034-A-1 (HNDS0181-01#F CNC27(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  345. BCHi034-A-2 (HNDS0181-01#F CNC33(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  346. BCHi034-A-3 (HNDS0181-01#F CC2(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  347. BCHi034-A-4 (HNDS0181-01#F CC7(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  348. BCHi035-A (HNDS0078-01#D)

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  349. BCHi035-A-1 (HNDS0078-01#D CNC2(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  350. BCHi035-A-2 (HNDS0078-01#D CNC6(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  351. BCHi035-A-3 (HNDS0078-01#D CC8(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  352. BCHi035-A-4 (HNDS0078-01#D CC18(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  353. BCHi036-A (HNDS0070-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  354. BCHi036-A-1 (HNDS0070-01#B CNC5(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  355. BCHi036-A-2 (HNDS0070-01#B CNC19(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  356. BCHi036-A-3 (HNDS0070-01#B CC1(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  357. BCHi036-A-4 (HNDS0070-01#B CC11(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  358. BCHi037-A (HNDS0072-01#C)

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  359. BCHi037-A-1 (HNDS0072-01#C CNC52(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  360. BCHi037-A-2 (HNDS0072-01#C CNC87(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  361. BCHi037-A-3 (HNDS0072-01#C CC20(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  362. BCHi037-A-4 (HNDS0072-01#C CC80(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  363. BCHi038-A (SAH0024-01#D and HNDS0165-01#D)

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  364. BCHi038-A-1 (HNDS0165-01#D CNC8(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  365. BCHi038-A-2 (HNDS0165-01#D CNC68(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  366. BCHi038-A-3 (HNDS0165-01#D CC15-20(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  367. BCHi038-A-4 (HNDS0165-01#D CC52(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  368. BCHi038-A-5 (HNDS0165-01#D CC19(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  369. BCHi038-A-6 (HNDS0165-01#D CC121(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  370. BCHi039-A (HNDS0128-01#C)

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  371. BCHi039-A-1 (HNDS0128-01#C CNC25-3(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  372. BCHi039-A-2 (HNDS0128-01#C CNC25-4(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  373. BCHi039-A-3 (HNDS0128-01#C CC19-10(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  374. BCHi039-A-4 (HNDS0128-01#C CC45-22(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  375. BCHi040-A (HNDS0130-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  376. BCHi040-A-1 (HNDS0130-01#B CNC8(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  377. BCHi040-A-2 (HNDS0130-01#B CNC50(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  378. BCHi040-A-3 (HNDS0130-01#B CC31(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  379. BCHi040-A-4 (HNDS0130-01#B CC67(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  380. BCHi041-A (HNDS0134-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  381. BCHi041-A-1 (HNDS0134-01#A CNC2(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  382. BCHi041-A-2 (HNDS0134-01#A CNC4(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  383. BCHi041-A-3 (HNDS0134-01#A CC43(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  384. BCHi041-A-4 (HNDS0134-01#A CC47(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  385. BCHi042-A (HNDS0161-01#E)

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  386. BCHi043-A (HNDS0056-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  387. BCHi043-B (HNDS0056-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  388. BCHi044-A (HNDS0048-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  389. BCHi044-B (HNDS0048-01#C)

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  390. BCHi045-A (HNDS0068-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  391. BCHi045-A-1 (HNDS0068-01#B CNC14(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  392. BCHi045-A-2 (HNDS0068-01#B CNC39(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  393. BCHi045-A-3 (HNDS0068-01#B CC3(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  394. BCHi045-A-4 (HNDS0068-01#B CC25(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  395. BCHi045-A-5 (HNDS0068-01#B CC29(-/-))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  396. BCHi046-A (HNDS0069-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  397. BCHi046-A-1 (HNDS0069-01#B CC26(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  398. BCHi046-A-2 (HNDS0069-01#B CC37(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  399. BCHi046-A-3 (HNDS0069-01#B Pass-Match-Control)

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  400. BCHi047-A (HNDS0056-02#A)

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  401. BCHi048-A (HNDS0048-03#B)

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  402. BCHi049-A (1383.1)

    United States Children's Hospital (BCH)
    Disease:

    Normal (average)

  403. BCHNi001-A (BCHi001-A)

    China Beijing Children′s Hospital：Department of Nephrology (BCHN)
    Disease:

    Bardet-biedl syndrome

  404. BCHNCi001-A

    China Beijing Children's Hospital, Center of Neurology (BCHNC)
    Disease:

    Early infantile developmental and epileptic encephalopathy

  405. BCHNCi003-A

    China Beijing Children's Hospital, Center of Neurology (BCHNC)
    Disease:

    Mitochondrial pyruvate carrier deficiency

  406. BCHNDi001-A

    China 徐超龙 (BCHND)
    Disease:

    Mitochondrial encephalomyopathy

  407. BCMi001-A (M22c5 and HSCC-003iPS-Sc5)

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal (average)

  408. BCMi001-B (M22c8 and HSCC-003iPS-Sc8)

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal (average)

  409. BCMi002-A (LZ02)

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal (average)

  410. BCMi003-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked intellectual disability syndrome

  411. BCMi004-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked intellectual disability syndrome

  412. BCMi005-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked intellectual disability syndrome

  413. BCMi006-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked intellectual disability syndrome

  414. BCMi007-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked intellectual disability syndrome

  415. BCRTi001-A (P01-1)

    Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)
    Disease:

    Fibrodysplasia ossificans progressiva

  416. BCRTi002-A (P02-1)

    Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)
    Disease:

    Fibrodysplasia ossificans progressiva

  417. BCRTi004-A

    Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)
    Disease:

    Normal (average)

  418. BCRTi005-A

    Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)
    Disease:

    Normal (average)

  419. BCRTi006-A

    Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)
    Disease:

    Focal segmental glomerulosclerosis

  420. BCRTi007-A

    Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)
    Disease:

    Polycystic kidney disease

  421. BCRTi009-A

    Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)
    Disease:

    Diabetic nephropathy

  422. BCRTi010-A

    Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)
    Disease:

    Normal (average)

  423. BCRTi011-A

    Germany Berlin-Brandenburg Center for Regenerative Therapies (BCRT)
    Disease:

    Neurofibromatosis type 1

  424. BFVSBi001-A

    United States Baszucki Family Vascular Surgery Biobank (BFVSB)
    Disease:

    Arterial calcification

  425. BFVSBi003-A

    United States Baszucki Family Vascular Surgery Biobank (BFVSB)
    Disease:

    Ehlers-danlos syndrome, vascular type

  426. BFVSBi004-A

    United States Baszucki Family Vascular Surgery Biobank (BFVSB)
    Disease:

    Ehlers-danlos syndrome, vascular type

  427. BFVSBi005-A

    United States Baszucki Family Vascular Surgery Biobank (BFVSB)
    Disease:

    Covid-19

  428. BFVSBi006-A

    United States Baszucki Family Vascular Surgery Biobank (BFVSB)
    Disease:

    Varicose veins

  429. BFVSBi007-A

    United States Baszucki Family Vascular Surgery Biobank (BFVSB)
    Disease:

    Melanoma

  430. BFVSBi008-A

    United States Baszucki Family Vascular Surgery Biobank (BFVSB)
    Disease:

    Loeys-dietz syndrome

  431. BGUi001-A (BGU01iPORhet)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    P450 oxidoreductase deficiency

  432. BGUi002-A (BGU02iPOR)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    P450 oxidoreductase deficiency

  433. BGUi003-A (BGU03iPOR)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    P450 oxidoreductase deficiency

  434. BGUi004-A (BGU101iCCHS)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    Congenital central hypoventilation syndrome

  435. BGUi005-A (BGU102iCCHS)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    Congenital central hypoventilation syndrome

  436. BGUi008-A (DCM-C)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    Left ventricular noncompaction cardiomyopathy

  437. BGUi009-A (DCM-O)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    Left ventricular noncompaction cardiomyopathy

  438. BGUi010-A (DCM-R)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    Left ventricular noncompaction cardiomyopathy

  439. BGUi011-A (BGU01iGRIN2D)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    Developmental and epileptic encephalopathy, 46

  440. BGUi012-A (BGU02iGRIN2D CTR)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    Normal (average)

  441. BGUi013-A (Omentum, BGU-hiPS and BGU-iPSCs)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    Normal (average)

  442. BGUi014-A (BGUiEMF and EMF-iPSCs)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    Normal (average)

  443. BGUi015-A (BGUiBJ)

    Israel Ben Gurion University of the Negev (BGU)
    Disease:

    Normal (average)

  444. BIHi001-A (BCRT-3 and BCRT#1)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  445. BIHi001-A-1 (iBCRT Cas9v1-3G-Kl.16)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  446. HMGUi001-A-18 (BIHi043-A SORL1_KO Cl B1)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  447. HMGUi001-A-19 (BIHi043-A SORL1_KO Cl F2)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  448. HMGUi001-A-44 (BIHi043-A-SORL_SNP_Cl-2)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Alzheimer disease

  449. BIHi001-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  450. BIHi001-B-1

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  451. BIHi001-B-7

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  452. BIHi001-B-8

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  453. BIHi001-B-9

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  454. BIHi001-B-10

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  455. BIHi001-B-13

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  456. BIHi002-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Autosomal recessive osteopetrosis 4

  457. BIHi004-A (NHDF Epi5 Cl5 iPSC)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  458. BIHi004-B (NHDF Epi5 Cl2 iPSC)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  459. BIHi005-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  460. BIHi005-A-4

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_myocardial infarction

  461. BIHi005-A-5

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_alzheimer's disease

  462. BIHi005-A-64

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  463. BIHi005-A-86

    Germany Berlin Institute of Health (BIH)
    Disease:

    Kit np_000213.1:p.d816v

  464. BIHi005-A-87 (hiPSCKITD816V-87)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Kit np_000213.1:p.d816v

  465. BIHi005-A-92

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  466. BIHi005-A-93

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  467. BIHi005-A-94

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obesity

  468. BIHi005-A-95

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  469. BIHi005-A-97

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obesity

  470. BIHi005-A-F

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obesity

  471. BIHi006-D

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  472. BIHi007-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  473. BIHi008-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  474. BIHi009-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  475. BIHi010-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  476. BIHi011-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  477. BIHi012-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  478. ZIPi013-B-1 (BIHi257-A-1)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  479. ZIPi013-B-2 (BIHi257-A-2)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  480. BIHi015-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  481. BIHi016-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  482. BIHi017-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  483. BIHi018-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  484. BIHi019-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  485. BIHi024-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  486. BIHi025-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  487. BIHi028-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  488. BIHi029-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  489. BIHi030-C

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  490. BIHi031-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  491. BIHi032-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  492. BIHi038-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  493. BIHi044-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Allan-herndon-dudley syndrome

  494. BIHi045-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Allan-herndon-dudley syndrome

  495. BIHi045-A-2

    Germany Berlin Institute of Health (BIH)
    Disease:

    Allan-herndon-dudley syndrome

  496. BIHi049-A (SCVI-112)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  497. WTSIi227-A-1 (WETU LRP2 KO)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Donnai-barrow syndrome

  498. BIHi250-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  499. BIHi261-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obesity due to pro-opiomelanocortin deficiency

  500. BIHi261-A-1

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obesity due to pro-opiomelanocortin deficiency

  501. BIHi263-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-related cognitive impairment

  502. BIHi264-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  503. BIHi265-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  504. BIHi266-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  505. BIHi267-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

  506. BIHi269-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  507. BIHi271-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  508. BIHi272-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-related cognitive impairment

  509. BIHi273-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  510. BIHi276-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

  511. BIHi289-C

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  512. BIHi289-E

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  513. BIHi290-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  514. BIHi290-D (BIHi290-CD8-cl.9)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  515. BIHi291-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  516. BIHi292-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Nasu-hakola disease

  517. BIHi294-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  518. BIHi296-A (03-17B)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  519. BIHi296-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  520. BIHi300-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-related cognitive impairment

  521. BIOi002-A

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Autosomal dominant optic atrophy

  522. BIOi003-A (LYN-C1-P6)

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Hereditary retinal dystrophy

  523. BIOi004-A

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Retinitis pigmentosa 33

  524. SIGi001-A-14 (SIGi001-A Bi-Allelic MAPT HA-tag)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  525. SIGi001-A-15 (SIGi001-A Dox inducible NGN2)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  526. SIGi001-A-16 (SIGi001-A-9 Bi-Allelic MAPT HA-tag)

    Denmark Bioneer (BION)
    Disease:

    Frontotemporal dementia

  527. SIGi001-A-17 (SIGi001-A-9 Dox inducible NGN2)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  528. SIGi001-A-18 (SIGi001-A-12 Bi-Allelic MAPT HA-tag #U28-12-P29-5)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  529. SIGi001-A-19 (SIGi001-A-12 Dox inducible NGN2)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  530. RCi004-A-1 (RCi004-A + HTT GC #H34-32_T34-23)

    Denmark Bioneer (BION)
    Disease:

    Huntington disease

  531. STBCi006-A-1 (ApoE KO)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  532. STBCi006-A-3 (ApoE 3/3)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  533. STBCi006-A-4 (ApoE 3/4)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  534. BIONi010-A (K1P53)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  535. BIONi010-B (K2P53 and BIONi010-B)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  536. BIONi010-C (BIONi010-C and K3P53)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  537. BIONi010-C-2 (BIONi010-C ApoE E3/E3 #H8 P32)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  538. BIONi010-C-3 (BIONi010-C ApoE KO #KO30 P30)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  539. BIONi010-C-4 (BIONi010-C ApoE E4/E4 #B44 P27)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  540. BIONi010-C-5 (BIONi010-C CD33 E2del #N14 P26)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  541. BIONi010-C-6 (BIONi010-C ApoE E2/E2)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  542. BIONi010-C-7 (BIONi010-C Trem2 R47H)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  543. BIONi010-C-8 (BIONi010-C Trem2 T66M and #Y5-80)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  544. BIONi010-C-9 (BIONi010-C CD33 KO)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  545. BIONi010-C-10 (HNF1AP291fsinsC +/- 54-5)

    Denmark Bioneer (BION)
    Disease:

    Mody

  546. BIONi010-C-11 (HNF1AP291fsinsC -/- 66-1)

    Denmark Bioneer (BION)
    Disease:

    Mody

  547. BIONi010-C-12 (HNF4ApR309C -/- 2-4)

    Denmark Bioneer (BION)
    Disease:

    Mody

  548. BIONi010-C-13 (BIONi010-C + NGN2 #I7-26)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  549. BIONi010-C-15 (BIONi010-C +dox inducible NGN2-GFP)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  550. BIONi010-C-17 (BIONi010-C TREM2 KO)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  551. BIONi010-C-18 (BIONi010-C TBK1 KO)

    Denmark Bioneer (BION)
    Disease:

    Obsolete_inflammatory disease

  552. BIONi010-C-19 (BIONi010-C IKBKE KO)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  553. BIONi010-C-24 (BIONi010-C Dox a-syn)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  554. BIONi010-C-25 (BIONi010-C heterozygous TREM2 KO)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  555. BIONi010-C-41 (BIONi010-C + iNGN2 Two-plasmid system/CRISPR-2)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  556. BIONi010-C-42 (BIONi010-C + iCRE AAVS1)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  557. BIONi010-C-43 (BIONi010-C + aSNCA-wt AAVS1)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  558. BIONi010-C-44 (BIONi010-C + aSNCA-A53T AAVS1)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  559. BIONi010-C-45 (BIONi010-C iCRE AAVS1 GBA1 LoxP EX5-6)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  560. BIONi010-C-48 (BIONi010-C hMDR1)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  561. BIONi010-C-49 (BIONi010-C + synapsin-m2rtTA + SNCA-wt)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  562. BIONi010-C-50 (BIONi010-C + synapsin-m2rtTA + SNCA-A53T)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  563. BIONi010-C-51 (BIONi010-C TNNI3-mCherry reporter)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  564. BIONi010-C-52 (BIONi010-C with an APOE 2/2 genotype (with two functional alleles in contrast to BIONi010-C-6))

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  565. BIONi010-C-53 (BIONi010-C with an APOE 3/3 genotype (with two functional alleles in contrast to BIONi010-C-2))

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  566. BIONi010-C-54 (BIONi010-C with an APOE 4/4 genotype (with two functional alleles in contrast to BIONi010-C-4))

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  567. BIONi010-C-55 (BIONi010-C TNNI3-mCherry/TNNI1-EGFP dual reporter cl. 74)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  568. BIONi010-C-64 (BIONi010-C-T2A-Nanoluciferase reporter cl. 29)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  569. BIONi010-C-70 (BIONi010-C with an APOE 2/2 genotype with an additional, homozygous christchurch mutation)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

  570. BIONi010-C-71 (BIONi010-C with an APOE 3/3 genotype with an additional, homozygous christchurch mutation)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

  571. BIONi010-C-72

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

  572. UKBi011-A-1 (iLB-AD + ApoE KO)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  573. UKBi011-A-2 (ApoE 2/2)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  574. UKBi011-A-3 (ApoE 3/3)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  575. UKBi011-A-4 (ApoE 3/4)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  576. BIONi013-A (H240715 47-1 and SAMEA4342502)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  577. BIONi014-A (H270715 47-1 and SAMEA4342566)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  578. BIONi015-A (H280715 47-1 and SAMEA4342649)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  579. BIONi016-A (H310715 47-1)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  580. BIONi017-A (H030815 47-1 and SAMEA4451663)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  581. BIONi018-A (H050815 48-4 and SAMEA4451665)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  582. BIONi019-A (H060815 48-3 and SAMEA4451667)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  583. BIONi020-A (H070815 47-2 and SAMEA4451669)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  584. BIONi021-A (H100815 48-2 and SAMEA4451671)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  585. BIONi022-A (H110815 47-2 and SAMEA4451673)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  586. BIONi023-A (H130815 47-4 and SAMEA4454014)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  587. BIONi024-A (H170815 47-2 and SAMEA4454016)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  588. BIONi025-A (H210815 48-3 and SAMEA4454018)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  589. BIONi026-A (H300715 48-3)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  590. BIONi027-A (H040815 48-1 and SAMEA4455499)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  591. BIONi028-A (H120815 48-1 and SAMEA4455501)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  592. BIONi029-A (H190815 47-1 and SAMEA4455503)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  593. BIONi030-A (H200815 47-1 and SAMEA4455505)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  594. BIONi031-A (H240815 48-2 and SAMEA4455507)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  595. BIONi032-A (H250815 48-1 and SAMEA4455509)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  596. BIONi033-A (H180615 and SAMEA4563389)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  597. BIONi034-A (H290715 and SAMEA4563391)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  598. BIONi035-A (H180815 and SAMEA4563393)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  599. BIONi037-A (16423 ApoE3/3 (control line))

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  600. BIONi037-A-1 (16423 ApoE KO)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  601. BIORTCi001-A (BAiPSC 000 and OSTiFGM2)

    Nigeria Biomedical Science Research and Training Centre (BIORTC)
    Disease:

    Normal (average)

  602. BIOTi001-A (BIOT-7183-PSEN1)

    Hungary BioTalentum Ltd. (BIOT)
    Disease:

    Obsolete_alzheimer's disease

  603. BIOTi003-A (BIOT-4828-LOAD and BIOT.201)

    Hungary BioTalentum Ltd. (BIOT)
    Disease:

    Alzheimer disease

  604. BIUi001-A (T1A1i-001)

    Israel Bar Ilan University (BIU)
    Disease:

    Obsolete: nuclear cell envelopathy

  605. BIUi002-A (T1A1i-002)

    Israel Bar Ilan University (BIU)
    Disease:

    Obsolete: nuclear cell envelopathy

  606. BJTTHi001-A

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Normal (average)

  607. BJTTHi001-A-1

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Obsolete_epilepsy

  608. BJTTHi001-A-2

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Dravet syndrome

    Disease:

    Obsolete_epilepsy

  609. BJTTHi001-A-3

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Obsolete_epilepsy

  610. BJTTHi001-A-4

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Obsolete_epilepsy

  611. BJTTHi001-A-5

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Obsolete_epilepsy

  612. BJTTHi003-A (CARASIL WHN1C2)

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Carasil syndrome

  613. BRCi014-A (1383D6 and HPS1006)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Normal (average)

  614. BRCi014-A-3 (MBP-TEZ)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Oligodendrocyte

  615. BRCi021-A (TUH1)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Cardiomyopathy

  616. BRCi024-A (HiPS-RTT_CUH01)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  617. BRCi025-A (HiPS-RTT_CUH02)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  618. BRCi026-A (HiPS-RTT_CUH05)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  619. BRCi027-A (HiPS-RTT_CUH06)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  620. BRCi036-A (HiPS-GLUT1DS1)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Classic glucose transporter type 1 deficiency syndrome

  621. BRCi037-A (HiPS-GLUT1DS2)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Classic glucose transporter type 1 deficiency syndrome

  622. BIONi037-A-2 (BIONi037-A ApoE2/2 #M10-7)

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

  623. BIONi037-A-3 (BIONi037-A ApoE3/4 #P10-22)

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

  624. BIONi037-A-4 (BIONi037-A ApoE4/4 #I10-53)

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

  625. BTHBIOi001-A (BiPSC-HXL-CNGA1)

    China Beijing Institute of Ophthalmology for BeijingTongren Hospital (BTHBIO)
    Disease:

    Retinitis pigmentosa

  626. BTHBIOi002-A

    China Beijing Institute of Ophthalmology for BeijingTongren Hospital (BTHBIO)
    Disease:

    Usher syndrome

  627. BTHBIOi003-A

    China Beijing Institute of Ophthalmology for BeijingTongren Hospital (BTHBIO)
    Disease:

    Leber congenital amaurosis

  628. BTHBIOi004-A

    China Beijing Institute of Ophthalmology for BeijingTongren Hospital (BTHBIO)
    Disease:

    Oculocutaneous albinism type 2

  629. BTHBIOi005-A

    China Beijing Institute of Ophthalmology for BeijingTongren Hospital (BTHBIO)
    Disease:

    Retinitis pigmentosa

  630. BTHBIOi006-A (RDH12-LY-M-BIPS-C2-211109)

    China Beijing Institute of Ophthalmology for BeijingTongren Hospital (BTHBIO)
    Disease:

    Leber congenital amaurosis

  631. BUCREMi001-A (iPSC-S6D63H-1-hom)

    United States Boston University (BUCREM)
    Disease:

    Lethal brain and heart developmental defects

  632. BUCREMi002-A (iPSC-S6D63H-3hom)

    United States Boston University (BUCREM)
    Disease:

    Lethal brain and heart developmental defects

  633. CABi002-A (OF0176-EYS02-C7 and EYS02-MiPS4F7)

    Spain CABIMER (Andalusian Molecular Biology and Regenerative Medicine Centre) (CAB)
    Disease:

    Retinitis pigmentosa

  634. CABi003-A (DH05 and AMDdh05-MiPS4F16)

    Spain CABIMER (Andalusian Molecular Biology and Regenerative Medicine Centre) (CAB)
    Disease:

    Age-related macular degeneration

  635. CAMi001-A (KiPS c1)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  636. CAMi002-A (FiPS 2a)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  637. CAMi002-B (FiPS 2b)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  638. CAMi002-C (FiPS 2c)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  639. CAMi004-A (AdiPS 1)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  640. CAMi005-A (O27Tat)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  641. CAMi005-B (2F8)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  642. CAMi014-A (A1ATD1)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Alpha-1-antitrypsin deficiency

  643. CBi001-A (XLC-348)

    United States Creative Bioarray (CB)
    Disease:

    Obsolete_schizophrenia

  644. CBi002-A (XLC303 and CSC-C00122)

    United States Creative Bioarray (CB)
    Disease:

    Obsolete_schizophrenia

  645. CBCi001-A (CS2BFUiALS-n2)

    United States Cedars-Sinai Biomanufacturing Center (CBC)
    Disease:

    Amyotrophic lateral sclerosis

  646. CBCHi001-A-1

    China Beijing Chest Hospital (CBCH)
    Disease:

    Hypertrophic cardiomyopathy

  647. CBDTi001-A

    India Institute for Stem Cell Science and Regenerative Medicine (CBDT)
    Disease:

    Normal (average)

  648. CBIGi001-A (AIW002-02 and IPSC0063)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  649. CBIGi001-A-1 (PRKN-KO, PRKN-KO/AIW002-02 and IPSC0070)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  650. CBIGi001-A-2 (PINK1-KO, PINK1-KO/AIW002-02 and IPSC0072)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  651. CBIGi001-A-3 (PINK1-KO/PRKN-KO/AIW002-02, PINK1-KO/PRKN-KO and IPSC0069)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  652. CBIGi001-A-4 (MAPT P301L/AIW002-02 and IPSC0065)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  653. CBIGi001-A-5 (MAPT-KO/AIW002-02 and IPSC0066)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  654. CBIGi001-A-6 (IPSC0067 and OFD1-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Intellectual disability

  655. CBIGi001-A-7 (IPSC0068 and OPTN-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  656. CBIGi001-A-8 (IPSC0071 and PINK1-3flag/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  657. CBIGi001-A-9 (IPSC0073 and PRKN A401D/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  658. CBIGi001-A-10 (IPSC0074 and PRKN W403A/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  659. CBIGi001-A-11 (IPSC0075 and PRKN Y143D/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  660. CBIGi001-A-12 (PRKN-V393D/AIW002-02 and IPSC0076)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  661. CBIGi001-A-13 (IPSC0078 and SCARB2-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  662. CBIGi001-A-14 (IPSC0079 and SH3GL2-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  663. CBIGi001-A-15 (SNCA A30P/AIW002-02 and IPSC0080)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  664. CBIGi001-A-16 (IPSC0081 and SNCA A53T/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  665. CBIGi001-A-17 (IPSC0082 and SNCA E46K/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  666. CBIGi001-A-18 (IPSC0083 and SNCA-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  667. CBIGi001-A-19 (IPSC0084 and SOD1 G93A/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  668. CBIGi001-A-20 (SPG11-KO/AIW002-02 and IPSC0085)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Intellectual disability

  669. CBIGi001-A-21 (IPSC0086 and SMPD-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  670. CBIGi001-A-22 (TARDBP-A382T/AIW002-02 and IPSC0089)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  671. CBIGi001-A-23 (TARDBP-G348C/AIW002-02 and IPSC0090)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  672. CBIGi001-A-24 (TMEM163-KO/AIW002-02 and IPSC0096)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  673. CBIGi001-A-25 (IPSC0097 and TMEM175-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  674. CBIGi001-A-26 (USP19-KO/AIW002-02 and IPSC0098)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  675. CBIGi001-A-27 (IPSC0099 and ARL13B-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Intellectual disability

  676. CBIGi001-A-28 (IPSC0100 and ASAH1-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  677. CBIGi001-A-29 (ATAXIN3-KO/AIW002-02 and IPSC0101)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Machado-joseph disease

  678. CBIGi001-A-30 (BIN3-KO/AIW002-02 and IPSC0102)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  679. CBIGi001-A-31 (IPSC0103 and C9ORF72-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  680. CBIGi001-A-32 (CDH12-KO/AIW002-02 and IPSC0104)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Intellectual disability

  681. CBIGi001-A-33 (CLCN3-KO/AIW002-02 and IPSC0105)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  682. CBIGi001-A-34 (CTSB-KO/AIW002-02 and IPSC0106)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  683. CBIGi001-A-35 (FAM49B(CYRIB)-KO/AIW002-02 and IPSC0107)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  684. CBIGi001-A-36 (IPSC0108 and FMR1-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Intellectual disability

  685. CBIGi001-A-37 (IPSC0109 and FUS-H517Q/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  686. CBIGi001-A-38 (IPSC0110 and FUS-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  687. CBIGi001-A-39 (IPSC0111 and GALC-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  688. CBIGi001-A-40 (IPSC0112 and GBA-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  689. CBIGi001-A-41 (IPSC0113 and GBAP1_promoter-KO/AIW002-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  690. CBIGi001-A-42 (IGSF9B-KO/AIW002-02 and IPSC0114)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  691. CBIGi001-A-43 (INPP5F-KO/AIW002-02 and IPSC0115)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  692. CBIGi001-A-44 (IP6K2-KO/AIW002-02 and IPSC0116)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  693. CBIGi001-A-45 (LRRK2-KO/AIW002-02 and IPSC0117)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  694. CBIGi001-B (IPSC0064)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  695. CBIGi001-C (IPSC0125 and AJG001-C4)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  696. CBIGi002-A (2890 (GBA W378G, heterozygous), 2890 and IPSC0001)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  697. CBIGi002-A-1 (GBA W378G-correction/2890, 2890-iso and IPSC0002)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  698. CBIGi003-A (3026, 3026 (GBA N370S, heterozygous) and IPSC0004)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  699. CBIGi003-A-1 (3026-iso, GBA N370S-correction/3026 and IPSC0005)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  700. CBIGi004-A (IPSC0034)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  701. CBIGi005-A (IPSC0003 and LRRK2 G2019S)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  702. CBIGi006-A (IPSC0006 and LRRK2 G2019S heterozygous)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  703. CBIGi006-A-1 (IPSC0007 and LRRK2 G2019S-correction)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  704. CBIGi007-A (IPSC0008 and TMEM175 Q65P heterozygous)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  705. CBIGi007-A-1 (IPSC0009 and TMEM175 Q65Q homozygous correction)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  706. CBIGi007-A-2 (IPSC0010 and TMEM175 P65P homozygous disease)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  707. CBIGi008-A (IPSC0011 and GBA T369M)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  708. CBIGi009-A (IPSC0012 and TMEM175 M393T homozygous)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  709. CBIGi009-A-1 (IPSC0013 and TMEM175 M393T homozygous correction)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  710. CBIGi009-B (TMEM175 M393T homozygous (CBIGi009) and IPSC0033)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  711. CBIGi010-A (SOD1 A4S and IPSC0014)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  712. CBIGi011-A (SOD1 I114T and IPSC0015)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  713. CBIGi012-A (IPSC0016)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  714. CBIGi013-A (IPSC0017 and LRRK2 M1646T (heterozygous))

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  715. CBIGi013-A-1 (LRRK2 M1646T correction and IPSC0018)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  716. CBIGi014-A (VAPB A2V and IPSC0019)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  717. CBIGi015-A (IPSC0020 and LRRK2 N551K-R1398H-K1423K (protective haplotype))

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  718. CBIGi016-A (IPSC0021 and Parkin homozygous deletion between exon 3 and 4)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  719. CBIGi017-A (IPSC0022)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  720. CBIGi018-A (AIW001-02 and IPSC0023)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  721. CBIGi018-A-1 (IPSC0024 and DENND5-KO/AIW001-02)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Intellectual disability

  722. CBIGi018-B (TD02 and IPSC0035)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  723. CBIGi019-A (IPSC0025)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  724. CBIGi020-A (IPSC0026)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  725. CBIGi021-A (GBA1 L324I and IPSC0027)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  726. CBIGi022-A (IPSC0028 and SOD1 I114T (CBIGi022-A))

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  727. CBIGi022-A-1 (SOD1 I114T correction (CBIGi022-A) and IPSC0029)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  728. CBIGi023-A (IPSC0030 and sporadic sALS+FTD)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  729. CBIGi024-A (IPSC0031 and SOD1 I144T (CBIGi024-A))

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  730. CBIGi025-A (IPSC0032)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  731. CBIGi026-A (IPSC0036)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  732. CBIGi026-B (IPSC0095)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  733. CBIGi027-A (LRRK2 G2385R (CBIGi027) and IPSC0037)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  734. CBIGi027-A-1 (IPSC0039 and LRRK2 G2385R (CBIGi027) correction)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  735. CBIGi028-A (IPSC0038)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  736. CBIGi029-A (IPSC0040)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  737. CBIGi030-A (IPSC0041)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  738. CBIGi031-A (IPSC0042)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  739. CBIGi032-A (IPSC0043)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  740. CBIGi032-A-1 (DENND5-KO(CBIGi032-A) and IPSC0061)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  741. CBIGi032-A-2 (IPSC0062 and EI2F2B-KO(het) (CBIGi032-A))

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  742. CBIGi032-A-3 (SOX10-P2A-mOrange and IPSC0126)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  743. CBIGi033-A (IPSC0044)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  744. CBIGi034-A (IPSC0045)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  745. CBIGi035-A (IPSC0046)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  746. CBIGi036-A (IPSC0047)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  747. CBIGi037-A (IPSC0048 and LRRK2 M1646T(CBIGi037-A))

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  748. CBIGi038-A (IPSC0049)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  749. CBIGi039-A (IPSC0050 and LRRK2 R1441H(CBIGi039-A))

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  750. CBIGi039-A-1 (IPSC0051 and LRRK2 R1441H(CBIGi039-A) correction)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  751. CBIGi040-A (IPSC0052 and LRRK2 N551K-R1398H-K1423K (protective haplotype) (CBIGi040-A))

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  752. CBIGi041-A (IPSC0053 and GBA L444P (CBIGi041-A))

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  753. CBIGi041-A-1 (IPSC0054 and GBA L444P (CBIGi041-A) correction)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  754. CBIGi042-A (IPSC0055 and GBA E326K (CBIGi042-A))

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  755. CBIGi042-A-1 (GBA E326K (CBIGi042-A) correction and IPSC0056)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  756. CBIGi043-A (IPSC0057)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  757. CBIGi044-A (LRRK2 N551K-R1398H-K1423K (protective haplotype)(CBIGi044-A) and IPSC0058)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  758. CBIGi044-A-1 (IPSC0059 and LRRK2 N551K (CBIGi044-A) correction)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  759. CBIGi044-A-2 (IPSC0060 and LRRK2 R1398H (CBIGi044-A) correction)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  760. CBIGi045-A (GBA L444P(CBIGi045-A) and IPSC0077)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  761. CBIGi046-A (IPSC0087)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  762. CBIGi046-B (IPSC0088)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Normal (average)

  763. CBIGi047-A (IPSC0091)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  764. CBIGi048-A (IPSC0092)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  765. CBIGi049-A (IPSC0093 and SOD1 I144T(CBIGi049-A))

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Amyotrophic lateral sclerosis

  766. CBIGi050-A (IPSC0094)

    Canada Clinical Biospecimen Imaging and Genetic (C-BIG) Repository (CBIG)
    Disease:

    Parkinson disease

  767. CBRCULi001-A (13-6545-1)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Normal (average)

  768. CBRCULi002-A (19-1035-10)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Myotonic dystrophy type 1

  769. CBRCULi003-A (59-0944-2)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Myotonic dystrophy type 1

  770. CBRCULi004-A (79-1660-2)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Myotonic dystrophy type 1

  771. CBRCULi005-A (91-3158-1)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Myotonic dystrophy type 1

  772. CBRCULi006-A (59-0116-24)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Normal (average)

  773. CBRCULi007-A (14-0730-1)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Myotonic dystrophy type 1

  774. CBRCULi008-A (522-0617-1)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Normal (average)

  775. CBRCULi009-A (522-1839-4)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Normal (average)

  776. CBRCULi010-A (GM00498E-1 and GM00498E clone 1)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Normal (average)

  777. CBRCULi011-A (GM00969F-2 and GM00969F clone 2)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Normal (average)

  778. CBRCULi012-A (GM04601 clone 21 and GM04601-21)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Myotonic dystrophy type 1

  779. CBRCULi013-A (GM04602-2 and GM04602 clone 2)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Myotonic dystrophy type 1

  780. CBRCULi014-A (AG09393A clone 3 and AG09393A-3)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Normal (average)

  781. CBRCULi015-A (GM23375-1 and GM23375 clone 1)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Congenital myotonic dystrophy

  782. CBRCULi016-A (SCN5A p.R219H-14C)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Obsolete_dilated cardiomyopathy

  783. CBRCULi016-A-1 (SCN5A p.R219H-14C-ISO)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Obsolete_dilated cardiomyopathy

  784. CBRCULi017-A (SCN5A p.R219-22B)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Normal (average)

  785. CBRCULi018-A (91-2032-7)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Myotonic dystrophy type 1

  786. CBRCULi019-A (19-1741-2)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Myotonic dystrophy type 1

  787. CBRCULi020-A (79-1761-15)

    Canada CERVO Brain Research Centre-Université Laval (CBRCUL)
    Disease:

    Myotonic dystrophy type 1

  788. CCMi001-A (DMD1)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Duchenne muscular dystrophy

  789. CCMi007-A (SAS1 C5)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  790. CCMi008-A (SAS2 C1)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  791. CCMi009-A (SAS3 C10)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  792. CCMi011-A (SAS7 C6)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  793. CCMi012-A (LMNA_SP_C3)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Dilated cardiomyopathy

  794. TMOi001-A-1 (hiPSC-CD34-GFP-3G6)

    Austria St. Anna Kinderkrebsforschung GmbH (CCRI)
    Disease:

    Normal (average)

  795. CDIi001-A (01279)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  796. CDIi002-A (01434)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  797. CDIi004-A (11713)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  798. CDIi011-A (21527)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  799. CDIi013-A (PPMI_3409 and FCDI_11287)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  800. CDIi014-A (FCDI_11292 and PPMI_4055)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  801. CDIi015-A (PPMI_3419 and FCDI_11294)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  802. CDIi016-A (PPMI_3411 and FCDI_11295)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  803. CDIi017-A (PPMI_3446 and FCDI_11296)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  804. CDIi018-A (PPMI_3234 and FCDI_11298)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  805. CDIi019-A (PPMI_52062 and FCDI_11299)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  806. CDIi019-A-1

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  807. CDIi019-A-2

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  808. CDIi020-A (PPMI_54144 and FCDI_11300)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  809. CDIi021-A (PPMI_3459 and FCDI_11301)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  810. CDIi022-A (FCDI_11302 and PPMI_3460)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  811. CDIi023-A (FCDI_11303 and PPMI_3448)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  812. CDIi024-A (FCDI_11305 and PPMI_51867)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  813. CDIi025-A (FCDI_11306 and PPMI_40273)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  814. CDIi026-A (FCDI_11307 and PPMI_51625)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  815. CDIi027-A (FCDI_11308 and PPMI_3186)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  816. CDIi028-A (PPMI_3664 and FCDI_11309)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  817. CDIi029-A (PPMI_3665 and FCDI_11310)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  818. CDIi030-A (FCDI_11311 and PPMI_3668)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  819. CDIi031-A (PPMI_3451 and FCDI_11312)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  820. CDIi032-A (FCDI_11313 and PPMI_3658)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  821. CDIi033-A (FCDI_11314 and PPMI_3465)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  822. CDIi034-A (PPMI_51440 and FCDI_11317)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  823. CDIi035-A (PPMI_51330 and FCDI_11318)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  824. CDIi036-A (PPMI_42072 and FCDI_11319)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  825. CDIi037-A (PPMI_52530 and FCDI_11321)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  826. CDIi038-A (FCDI_11323 and PPMI_53339)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  827. CDIi039-A (FCDI_11325 and PPMI_56761)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  828. CDIi040-A (FCDI_11327 and PPMI_3220)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  829. CDIi041-A (FCDI_11328 and PPMI_56435)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  830. CDIi042-A (PPMI_41486 and FCDI_11329)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  831. CDIi043-A (PPMI_54262 and FCDI_11331)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  832. CDIi044-A (PPMI_50184 and FCDI_11334)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  833. CDIi045-A (FCDI_11337 and PPMI_3952)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  834. CDIi046-A (FCDI_11340 and PPMI_56779)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  835. CDIi047-A (FCDI_11341 and PPMI_3471)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  836. CDIi048-A (PPMI_3453 and FCDI_11342)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  837. CDIi049-A (PPMI_3480 and FCDI_11343)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  838. CDIi050-A (PPMI_4098 and FCDI_11344)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  839. CDIi050-A-1

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  840. CDIi050-A-2

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  841. CDIi051-A (PPMI_3452 and FCDI_11345)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  842. CDIi052-A (PPMI_4091 and FCDI_11346)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  843. CDIi053-A (PPMI_3422 and FCDI_11347)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  844. CDIi054-A (FCDI_11348 and PPMI_50086)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  845. CDIi055-A (FCDI_11349 and PPMI_60003)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  846. CDIi056-A (PPMI_51971 and FCDI_11353)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  847. CDIi057-A (PPMI_56954 and FCDI_11355)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  848. CDIi058-A (FCDI_11362 and PPMI_51755)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  849. CDIi059-A (PPMI_52828 and FCDI_11363)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  850. CDIi060-A (FCDI_11370 and PPMI_55251)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  851. CDIi061-A (FCDI_11371 and PPMI_55380)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  852. CDIi062-A (FCDI_11436 and PPMI_90456)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  853. CDIi063-A (FCDI_11437 and PPMI_3473)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  854. CDIi064-A (PPMI_3475 and FCDI_11438)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  855. CDIi065-A (PPMI_3588 and FCDI_11442)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  856. CDIi066-A (FCDI_11446 and PPMI_4111)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  857. CDIi067-A (FCDI_11447 and PPMI_3960)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  858. CDIi068-A (FCDI_11448 and PPMI_51518)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  859. CDIi069-A (PPMI_3666 and FCDI_11449)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  860. CDIi070-A (FCDI_11450 and PPMI_3966)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  861. CDIi071-A (PPMI_4108 and FCDI_11455)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  862. CDIi072-A (FCDI_11459 and PPMI_4101)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  863. CDIi073-A (PPMI_52400 and FCDI_11460)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  864. CDIi074-A (PPMI_54908 and FCDI_11462)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  865. CDIi075-A (PPMI_54991 and FCDI_11463)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  866. CDIi076-A (PPMI_56680 and FCDI_11465)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  867. CDIi077-A (PPMI_3469 and FCDI_11468)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  868. CDIi078-A (FCDI_11469 and PPMI_3467)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  869. CDIi079-A (PPMI_57670 and FCDI_11471)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  870. CDIi080-A (FCDI_11473 and PPMI_51844)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  871. CDIi081-A (PPMI_57447 and FCDI_11474)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  872. CDIi082-A (PPMI_4099 and FCDI_11475)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  873. CDIi083-A (PPMI_52524 and FCDI_11478)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  874. CDIi084-A (FCDI_11483 and PPMI_57292)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  875. CDIi085-A (FCDI_11484 and PPMI_3954)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  876. CDIi086-A (PPMI_18567 and FCDI_11486)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  877. CDIi087-A (PPMI_4106 and FCDI_11491)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  878. CDIi088-A (PPMI_4107 and FCDI_11492)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  879. CDIi089-A (FCDI_11493 and PPMI_4109)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  880. CDIi090-A (FCDI_11494 and PPMI_4110)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  881. CDIi091-A (FCDI_11498 and PPMI_51714)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  882. CDIi092-A (FCDI_11500 and PPMI_56169)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  883. CDIi093-A (PPMI_3953 and FCDI_11505)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  884. CDIi094-A (FCDI_11508 and PPMI_52517)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  885. CDIi095-A (FCDI_11512 and PPMI_53988)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  886. CDIi096-A (FCDI_11526 and PPMI_57961)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  887. CDIi097-A (FCDI_11527 and PPMI_3591)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  888. CDIi098-A (FCDI_11545 and PPMI_52932)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  889. CDIi099-A (FCDI_11546 and PPMI_53518)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  890. CDIi100-A (FCDI_11555 and PPMI_42378)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  891. CDIi101-A (FCDI_11556 and PPMI_40760)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  892. CDIi102-A (FCDI_11557 and PPMI_41430)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  893. CDIi103-A (FCDI_11571 and PPMI_58182)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  894. CDIi104-A (FCDI_11578 and PPMI_54048)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  895. CDIi105-A (PPMI_41568 and FCDI_14555)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  896. CEBi001-A (Cellartis Human iPS Cell Line 22)

    France Takara Bio Europe AB (former Cellartis) (CEB)
    Disease:

    Normal (average)

  897. CEGHUi001-A (iPSC_CEGH_C2)

    Brazil Human Genome and Stem Cell Research Center, University of São Paulo (CEGHU)
    Disease:

    Normal (average)

  898. CENSOi001-B (FB78R2c2 and CENSOi249)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  899. CENSOi002-B (FB74R2c4 and CENSOi261)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  900. CENSOi003-B (FB79R2c6 and CENSOi258)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  901. CENSOi005-A (FB76R2c5 and CENSOi245)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  902. CENSOi007-A (FB75R2c5 and CENSOi255)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  903. CENSOi008-A (FB77R2c3 and CENSOi260)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Myotonic dystrophy type 1

  904. CHCMUi001-A

    China Children's hospital of Chongqing Medical University (CHCMU)
    Disease:

    Activated pi3k-delta syndrome

  905. CHCMUi002-A

    China Children's hospital of Chongqing Medical University (CHCMU)
    Disease:

    Chronic granulomatous disease

  906. CHDIi001-A (#1c8 and CHDI-90002149)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  907. CHDIi002-A (#2c3 and CHDI-90002150)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  908. CHDIi003-A (#3c1 and CHDI-90002151)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  909. CHDIi004-A (#4c2 and CHDI-90002152)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  910. CHDIi005-A (#5c4 and CHDI-90002153)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  911. CHDIi006-A (#6c7 and CHDI-90002154)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  912. CHDIi008-A (#8c3 and CHDI-90002156)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  913. CHDIi010-A (#10c2 and CHDI-90002158)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  914. CHDIi011-A (#11c2 and CHDI-90002159)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  915. CHDIi013-A (#13c5 and CHDI-90002161)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  916. CHDIi014-A (#14c1 and CHDI-90002162)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  917. CHDIi016-A (#16c6 and CHDI-90002164)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  918. CHDIi017-A (#17c1 and CHDI-90002165)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  919. CHDIi018-A (#18c1 and CHDI-90002166)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  920. CHDIi019-A (#19c9 and CHDI-90002167)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  921. CHDIi020-A (#20c2 and CHDI-90002168)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  922. CHDIi021-A (#21c5 and CHDI-90002169)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  923. CHDIi022-A (#22c1 and CHDI-90002170)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  924. CHDIi023-A (#23c8 and CHDI-90002171)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  925. CHDIi024-A (#24c7 and CHDI-90002172)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  926. CHDIi026-A (#26c3 and CHDI-90002174)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  927. CHDIi027-A (#27c4 and CHDI-90002175)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  928. CHDIi028-A (#28c3 and CHDI-90002176)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  929. CHDIi029-A (#29c4 and CHDI-90002177)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  930. CHDIi031-A (#31c1 and CHDI-90002179)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  931. CHDIi033-A (#104c2 and CHDI-90002181)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  932. CHDIi034-A (#105c1 and CHDI-90002182)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  933. CHDIi035-A (#108c5 and CHDI-90002183)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  934. CHDIi036-A (#110c5 and CHDI-90002184)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  935. CHDIi038-A (#112c7 and CHDI-90002186)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  936. CHDIi040-A (#115c6 and CHDI-90002188)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  937. CHDIi041-A (#116c2 and CHDI-90002189)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  938. CHDIi042-A (#117c5 and CHDI-90002190)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  939. CHDIi043-A (#118c6 and CHDI-90002191)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  940. CHDIi044-A (#120c3 and CHDI-90002192)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  941. CHDIi045-A (#121c6 and CHDI-90002193)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  942. CHDIi046-A (#122c1 and CHDI-90002194)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  943. CHDIi047-A (#123c6 and CHDI-90002195)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  944. CHDIi048-A (#125c2 and CHDI-90002196)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  945. CHDIi049-A (#127c2 and CHDI-90002197)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  946. CHDIi050-A (#128c3 and CHDI-90002198)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  947. CHDIi051-A (#129c1 and CHDI-90002199)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  948. CHDIi054-A (#132c3 and CHDI-90002202)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  949. CHDIi055-A (#133c5 and CHDI-90002203)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  950. CHDIi056-A (#134c3 and CHDI-90002204)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  951. CHDTRi001-B (HT953B and iSP1.2.2B)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Cln3

  952. CHDTRi002-B (HT954B and iSP5.2.1B)

    United States Division of Translational Research, NICHD, NIH (CHDTR)

  953. CHDTRi003-A (HT955A and iSP5.2.2A)

    United States Division of Translational Research, NICHD, NIH (CHDTR)

  954. CHDTRi004-B (HT956B and iSP8.2.1B)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Cln3

  955. CHDTRi005-A (iSP10.2.1A and HT957A)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Cln3

  956. CHDTRi006-E (HT958E and iSP29.2.2E)

    United States Division of Translational Research, NICHD, NIH (CHDTR)

  957. CHDTRi007-A (HT1174-A)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Noonan syndrome

  958. CHDTRi008-A (HT1175-A)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Noonan syndrome

  959. CHDTRi009-A (HT1176-A)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Noonan syndrome

  960. CHDTRi010-A

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Noonan syndrome

  961. CHINTAi001-A (iCON-001)

    India CHINTA (CHINTA)
    Disease:

    Normal (average)

  962. CHINTAi002-A (iCON-002)

    India CHINTA (CHINTA)
    Disease:

    Normal (average)

  963. CHINTAi004-A (iMDD-001 and CUPi004-A)

    India CHINTA (CHINTA)
    Disease:

    Unipolar depression

  964. CHINTAi005-A (iMDD-002 and CUPi005-A)

    India CHINTA (CHINTA)
    Disease:

    Unipolar depression

  965. CHOCi005-A

    United States CHOC Children's (CHOC)
    Disease:

    Gm1 gangliosidosis

  966. CHOPi001-A (CHOPJMML1854)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Juvenile myelomonocytic leukemia

  967. CHOPi005-A (LD0638.0A)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Hypomyelination with atrophy of basal ganglia and cerebellum

  968. CHOPi006-A (LD0313.0)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Hypomyelination with atrophy of basal ganglia and cerebellum

  969. CHOPi007-A

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Hypomyelination with atrophy of basal ganglia and cerebellum

  970. CHOPi008-A (TMD145.T21.G1S)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Transient abnormal myelopoiesis associated with down syndrome

  971. CHOPi008-B (TMD145.E46.G1S)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Transient abnormal myelopoiesis associated with down syndrome

  972. CHOPi008-C (DS145.T21.G1)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Transient abnormal myelopoiesis associated with down syndrome

  973. CHOPi012-A (CHOPACTG2-R257C)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Obsolete_megacystis-microcolon-intestinal hypoperistalsis syndrome 5

  974. CHOPi013-A (CHOPWT17_TPM1KOc28)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Normal (average)

  975. CHOPi014-A (CHOPWT15)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Normal (average)

  976. CHSUi001-A

    China Children’s Hospital Affiliated to Shandong University, (CHSU)
    Disease:

    Severe combined immunodeficiency

  977. CHSUi002-A

    China Children’s Hospital Affiliated to Shandong University, (CHSU)
    Disease:

    Hatipoglu immunodeficiency syndrome

  978. CHULAi001-A (GPDi001-A)

    Thailand Chulalongkorn University (CHULA)
    Disease:

    Glucose-6-phosphate dehydrogenase deficiency

  979. CHUQi001-A (522-2666-2 and SAMEA104271492)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Myotonic dystrophy type 1

  980. CHUQi002-A (ARSM44081223)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  981. CHUQi003-A (ARSM19061223)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  982. CHUQi004-A (ARSF50111122)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  983. CHUQi005-A (ARSF29170521)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  984. CHUQi006-A (ARSF31280521)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  985. CHUQi007-A (ARSM47280521)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  986. CHUQi008-A (ARSM42081221)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  987. CHUQi009-A (ARSF56190702)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  988. CHUQi010-A (ARSM50190702)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  989. CHUVi001-A

    Switzerland Centre Hospitalier Universitaire Vaudois (CHUV)
    Disease:

    Normal (average)

  990. CHWi001-A

    China The centre of prenatal diagnosis, The Central Hospital of Wenzhou (CHW)
    Disease:

    Intellectual disability

  991. CHZJUi001-A

    China Children’s Hospital (CHZJU)
    Disease:

    Dilated cardiomyopathy

  992. CIAUi002-C (UBC3 M1)

    Australia Centenary Institute of Cancer Medicine and Cell Biology (CIAU)
    Disease:

    Left bundle branch block

    Disease:

    Nonischemic cardiomyopathy

  993. CIAUi003-A (MCCIi005-A-1 and BFC4)

    Australia Centenary Institute of Cancer Medicine and Cell Biology (CIAU)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia 2

  994. CIAUi003-A-1 (BFC4-C and BFC4-CRISPR-corrected)

    Australia Centenary Institute of Cancer Medicine and Cell Biology (CIAU)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia 2

  995. CIBIOi007-A (P1C12_LDhiPSC_Laf)

    Italy Università degli Studi di Trento (CIBIO)
    Disease:

    Lafora disease

  996. CIGLi001-A (RPChiPS8023G1, iPSC TBX4 WT, StemRNA™ Human iPSC 802-3G and SYNTHEGO 802-30F)

    United States Center for Infection and Genomics of the Lung (CIGL)
    Disease:

    Normal (average)

  997. CIGLi001-A-1 (SYNTHEGO 802-30F MUT and iPSC TBX4 MUT)

    United States Center for Infection and Genomics of the Lung (CIGL)
    Disease:

    Normal (average)

  998. CIMHi001-A (CIMHi44f028#4)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  999. CIMHi002-A (CIMHi29m067#3)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  1000. CIMHi003-A (CIMHi23m035#2)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  1001. CIMHi004-A (CIMHi24f007#4)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  1002. CIMHi005-A (CIMHi25f100#5)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  1003. CIMRi001-A (GM27291)

    United States Coriell Institute for Medical Research (CIMR)
    Disease:

    Vici syndrome

  1004. CIPi001-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)
    Disease:

    Self-limited infantile epilepsy

  1005. CIPi002-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)

  1006. CIPi004-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)

  1007. CIPi005-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  1008. CIRAi005-A (F2KU1#4 and F2KU1)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  1009. CIRAi005-A-1 (IsC2-F2KU1#4 and IsC-F2KU1)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  1010. CIRAi006-A (F2KU2#17 and F2KU2)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  1011. CIRAi006-A-1 (IsC-F2KU2 and IsC41-F2KU2#17)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  1012. CIRMi001-A (CW13000)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1013. CIRMi002-A (CW13002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1014. CIRMi003-A (CW13003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1015. CIRMi004-A (CW13005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1016. CIRMi005-A (CW13006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1017. CIRMi006-A (CW13009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1018. CIRMi007-A (CW13011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1019. CIRMi008-A (CW13016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1020. CIRMi009-A (CW13017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1021. CIRMi010-A (CW13018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1022. CIRMi011-A (CW13020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1023. CIRMi012-A (CW13021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1024. CIRMi013-A (CW13023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1025. CIRMi014-A (CW13024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1026. CIRMi015-A (CW13025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1027. CIRMi016-A (CW13026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1028. CIRMi017-A (CW13028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1029. CIRMi018-A (CW13029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1030. CIRMi019-A (CW13030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1031. CIRMi020-A (CW13031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1032. CIRMi021-A (CW13032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1033. CIRMi022-A (CW13033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1034. CIRMi023-A (CW13034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1035. CIRMi024-A (CW13037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1036. CIRMi025-A (CW13038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1037. CIRMi026-A (CW13041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1038. CIRMi027-A (CW13042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1039. CIRMi028-A (CW13044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1040. CIRMi029-A (CW13045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1041. CIRMi030-A (CW13047)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1042. CIRMi031-A (CW13048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1043. CIRMi032-A (CW13049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1044. CIRMi033-A (CW13052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1045. CIRMi034-A (CW13053)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1046. CIRMi035-A (CW13055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1047. CIRMi036-A (CW13060)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1048. CIRMi037-A (CW13061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1049. CIRMi038-A (CW13063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1050. CIRMi039-A (CW13064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1051. CIRMi040-A (CW13065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1052. CIRMi041-A (CW13066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1053. CIRMi042-A (CW13067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1054. CIRMi043-A (CW13070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1055. CIRMi044-A (CW13072)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1056. CIRMi045-A (CW13073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1057. CIRMi046-A (CW13074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1058. CIRMi047-A (CW13075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1059. CIRMi048-A (CW13076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1060. CIRMi049-A (CW13077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1061. CIRMi050-A (CW13079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1062. CIRMi051-A (CW13088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1063. CIRMi052-A (CW13092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1064. CIRMi053-A (CW13093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1065. CIRMi054-A (CW13094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1066. CIRMi055-A (CW13095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1067. CIRMi056-A (CW13097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1068. CIRMi057-A (CW13098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1069. CIRMi058-A (CW13105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1070. CIRMi059-A (CW13107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1071. CIRMi060-A (CW13108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1072. CIRMi061-A (CW13109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1073. CIRMi062-A (CW13111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1074. CIRMi063-A (CW13112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1075. CIRMi064-A (CW13113)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1076. CIRMi065-A (CW13054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1077. CIRMi066-A (CW13069)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1078. CIRMi067-A (CW50049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1079. CIRMi068-A (CW50001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1080. CIRMi069-A (CW50005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1081. CIRMi070-A (CW50007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1082. CIRMi071-A (CW50010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1083. CIRMi072-A (CW50015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1084. CIRMi073-A (CW50017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1085. CIRMi074-A (CW50020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1086. CIRMi075-A (CW50030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1087. CIRMi076-A (CW50048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1088. CIRMi077-A (CW50057)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1089. CIRMi078-A (CW50077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1090. CIRMi079-A (CW50080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1091. CIRMi080-A (CW50081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1092. CIRMi081-A (CW50083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1093. CIRMi082-A (CW50084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1094. CIRMi083-A (CW50085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1095. CIRMi084-A (CW50087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1096. CIRMi085-A (CW50088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1097. CIRMi086-A (CW50089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1098. CIRMi087-A (CW50090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1099. CIRMi088-A (CW50091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1100. CIRMi089-A (CW50092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1101. CIRMi090-A (CW50100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1102. CIRMi091-A (CW50102)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1103. CIRMi092-A (CW50103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1104. CIRMi093-A (CW50105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1105. CIRMi094-A (CW50124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1106. CIRMi095-A (CW50125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1107. CIRMi096-A (CW50135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1108. CIRMi097-A (CW50140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1109. CIRMi098-A (CW50151)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1110. CIRMi099-A (CW50163)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1111. CIRMi100-A (CW50164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1112. CIRMi101-A (CW50002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1113. CIRMi102-A (CW50003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1114. CIRMi103-A (CW50004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1115. CIRMi104-A (CW50006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1116. CIRMi105-A (CW50008)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1117. CIRMi106-A (CW50009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1118. CIRMi107-A (CW50013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1119. CIRMi108-A (CW50016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1120. CIRMi109-A (CW50018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1121. CIRMi110-A (CW50019)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1122. CIRMi111-A (CW50021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1123. CIRMi112-A (CW50022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1124. CIRMi113-A (CW50023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1125. CIRMi114-A (CW50024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1126. CIRMi115-A (CW50025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1127. CIRMi116-A (CW50026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1128. CIRMi117-A (CW50027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1129. CIRMi118-A (CW50028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1130. CIRMi119-A (CW50029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1131. CIRMi120-A (CW50032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1132. CIRMi121-A (CW50033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1133. CIRMi122-A (CW50034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1134. CIRMi123-A (CW50035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1135. CIRMi124-A (CW50036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1136. CIRMi125-A (CW50037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1137. CIRMi126-A (CW50038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1138. CIRMi127-A (CW50039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1139. CIRMi128-A (CW50040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1140. CIRMi129-A (CW50041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1141. CIRMi130-A (CW50042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1142. CIRMi131-A (CW50043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1143. CIRMi132-A (CW50044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1144. CIRMi133-A (CW50045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1145. CIRMi134-A (CW50046)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1146. CIRMi135-A (CW50047)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1147. CIRMi136-A (CW50050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1148. CIRMi137-A (CW50051)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1149. CIRMi138-A (CW50052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1150. CIRMi139-A (CW50054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1151. CIRMi140-A (CW50055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1152. CIRMi141-A (CW50056)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1153. CIRMi142-A (CW50058)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1154. CIRMi143-A (CW50059)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1155. CIRMi144-A (CW50060)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1156. CIRMi145-A (CW50061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1157. CIRMi146-A (CW50062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1158. CIRMi147-A (CW50063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1159. CIRMi148-A (CW50064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1160. CIRMi149-A (CW50065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1161. CIRMi150-A (CW50066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1162. CIRMi151-A (CW50067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1163. CIRMi152-A (CW50068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1164. CIRMi153-A (CW50069)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1165. CIRMi154-A (CW50070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1166. CIRMi155-A (CW50071)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1167. CIRMi156-A (CW50072)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1168. CIRMi157-A (CW50073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1169. CIRMi158-A (CW50074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1170. CIRMi159-A (CW50075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1171. CIRMi160-A (CW50076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1172. CIRMi161-A (CW50078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1173. CIRMi162-A (CW50079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1174. CIRMi163-A (CW50082)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1175. CIRMi164-A (CW50086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1176. CIRMi165-A (CW50093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1177. CIRMi166-A (CW50094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1178. CIRMi167-A (CW50095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1179. CIRMi168-A (CW50096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1180. CIRMi169-A (CW50097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1181. CIRMi170-A (CW50099)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1182. CIRMi171-A (CW50101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1183. CIRMi172-A (CW50104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1184. CIRMi173-A (CW50106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1185. CIRMi174-A (CW50107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1186. CIRMi175-A (CW50108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1187. CIRMi176-A (CW50109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1188. CIRMi177-A (CW50111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1189. CIRMi178-A (CW50112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1190. CIRMi179-A (CW50113)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1191. CIRMi180-A (CW50114)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1192. CIRMi181-A (CW50115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1193. CIRMi182-A (CW50117)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1194. CIRMi183-A (CW50118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1195. CIRMi184-A (CW50119)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1196. CIRMi185-A (CW50120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1197. CIRMi186-A (CW50121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1198. CIRMi187-A (CW50122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1199. CIRMi188-A (CW50123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1200. CIRMi189-A (CW50126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1201. CIRMi190-A (CW50127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1202. CIRMi191-A (CW50128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1203. CIRMi192-A (CW50129)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1204. CIRMi193-A (CW50130)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1205. CIRMi194-A (CW50131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1206. CIRMi195-A (CW50132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1207. CIRMi196-A (CW50133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1208. CIRMi197-A (CW50134)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1209. CIRMi198-A (CW50136)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1210. CIRMi199-A (CW50137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1211. CIRMi200-A (CW50138)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1212. CIRMi201-A (CW50139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1213. CIRMi202-A (CW50141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1214. CIRMi203-A (CW50142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1215. CIRMi204-A (CW50143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1216. CIRMi205-A (CW50144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1217. CIRMi206-A (CW50145)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1218. CIRMi207-A (CW50147)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1219. CIRMi208-A (CW50148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1220. CIRMi209-A (CW50149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1221. CIRMi210-A (CW50150)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1222. CIRMi211-A (CW50152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1223. CIRMi212-A (CW50153)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1224. CIRMi213-A (CW50155)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1225. CIRMi214-A (CW50156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1226. CIRMi215-A (CW50157)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1227. CIRMi216-A (CW50158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1228. CIRMi217-A (CW50159)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1229. CIRMi218-A (CW50161)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1230. CIRMi219-A (CW50162)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1231. CIRMi220-A (CW50165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1232. CIRMi221-A (CW50166)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1233. CIRMi222-A (CW50167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1234. CIRMi223-A (CW50168)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1235. CIRMi224-A (CW50169)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1236. CIRMi225-A (CW50170)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1237. CIRMi226-A (CW50173)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1238. CIRMi227-A (CW50174)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1239. CIRMi228-A (CW50175)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1240. CIRMi229-A (CW50176)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1241. CIRMi230-A (CW50177)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1242. CIRMi231-A (CW12000)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypoplasia of the optic nerve

  1243. CIRMi232-A (CW12001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1244. CIRMi233-A (CW12002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypoplasia of the optic nerve

  1245. CIRMi234-A (CW12003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1246. CIRMi235-A (CW12004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1247. CIRMi236-A (CW80003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1248. CIRMi237-A (CW80007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1249. CIRMi238-A (CW80008)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1250. CIRMi239-A (CW80009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1251. CIRMi240-A (CW80010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1252. CIRMi241-A (CW80011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1253. CIRMi242-A (CW80012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1254. CIRMi243-A (CW80014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1255. CIRMi244-A (CW80053)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1256. CIRMi245-A (CW80054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1257. CIRMi246-A (CW80018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1258. CIRMi247-A (CW80019)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1259. CIRMi248-A (CW80055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1260. CIRMi249-A (CW80021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1261. CIRMi250-A (CW80022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1262. CIRMi251-A (CW80024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1263. CIRMi252-A (CW80025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1264. CIRMi253-A (CW80026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1265. CIRMi254-A (CW80027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1266. CIRMi255-A (CW80028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1267. CIRMi256-A (CW80030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1268. CIRMi257-A (CW80031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1269. CIRMi258-A (CW80038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1270. CIRMi259-A (CW80040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1271. CIRMi260-A (CW80041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1272. CIRMi261-A (CW80042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1273. CIRMi262-A (CW80043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1274. CIRMi263-A (CW80044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1275. CIRMi264-A (CW80048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1276. CIRMi265-A (CW80049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1277. CIRMi266-A (CW80050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1278. CIRMi267-A (CW70001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1279. CIRMi268-A (CW70002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1280. CIRMi269-A (CW70004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1281. CIRMi270-A (CW70005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1282. CIRMi271-A (CW70006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1283. CIRMi272-A (CW70007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1284. CIRMi273-A (CW70008)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1285. CIRMi274-A (CW70009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1286. CIRMi275-A (CW70011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1287. CIRMi276-A (CW70012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1288. CIRMi277-A (CW70013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1289. CIRMi278-A (CW70014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1290. CIRMi279-A (CW70015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1291. CIRMi280-A (CW70016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1292. CIRMi281-A (CW70017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1293. CIRMi282-A (CW70018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1294. CIRMi283-A (CW70019)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1295. CIRMi284-A (CW70021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1296. CIRMi285-A (CW70022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1297. CIRMi286-A (CW70028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1298. CIRMi287-A (CW70029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1299. CIRMi288-A (CW70030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1300. CIRMi289-A (CW70032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1301. CIRMi290-A (CW70033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1302. CIRMi291-A (CW70034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1303. CIRMi292-A (CW70035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1304. CIRMi293-A (CW70036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1305. CIRMi294-A (CW70037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1306. CIRMi295-A (CW70038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1307. CIRMi296-A (CW70039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1308. CIRMi297-A (CW70040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1309. CIRMi298-A (CW70041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1310. CIRMi299-A (CW70042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1311. CIRMi300-A (CW70043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1312. CIRMi301-A (CW70044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1313. CIRMi302-A (CW70045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1314. CIRMi303-A (CW70047)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1315. CIRMi304-A (CW70048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1316. CIRMi305-A (CW70049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1317. CIRMi306-A (CW70050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1318. CIRMi307-A (CW70052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1319. CIRMi308-A (CW70056)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1320. CIRMi309-A (CW70057)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1321. CIRMi310-A (CW70059)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1322. CIRMi311-A (CW70060)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetes mellitus

  1323. CIRMi312-A (CW70061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1324. CIRMi313-A (CW70063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinal vein occlusion

  1325. CIRMi314-A (CW70064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1326. CIRMi315-A (CW70066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1327. CIRMi316-A (CW70071)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1328. CIRMi317-A (CW70072)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1329. CIRMi318-A (CW70073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1330. CIRMi319-A (CW70075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1331. CIRMi320-A (CW70077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1332. CIRMi321-A (CW70079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1333. CIRMi322-A (CW70081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1334. CIRMi323-A (CW70085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1335. CIRMi324-A (CW70086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1336. CIRMi325-A (CW70087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1337. CIRMi326-A (CW70088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1338. CIRMi327-A (CW70089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1339. CIRMi328-A (CW70090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1340. CIRMi329-A (CW70091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1341. CIRMi330-A (CW70092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1342. CIRMi331-A (CW70093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1343. CIRMi332-A (CW70094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1344. CIRMi333-A (CW70096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1345. CIRMi334-A (CW70097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1346. CIRMi335-A (CW70098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1347. CIRMi336-A (CW70100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1348. CIRMi337-A (CW70101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1349. CIRMi338-A (CW70102)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1350. CIRMi339-A (CW70103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1351. CIRMi340-A (CW70104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1352. CIRMi341-A (CW70105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1353. CIRMi342-A (CW70106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1354. CIRMi343-A (CW70107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1355. CIRMi344-A (CW70108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1356. CIRMi345-A (CW70109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1357. CIRMi346-A (CW70110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1358. CIRMi347-A (CW70111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1359. CIRMi348-A (CW70112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1360. CIRMi349-A (CW70114)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1361. CIRMi350-A (CW70115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1362. CIRMi351-A (CW70116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1363. CIRMi352-A (CW70117)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1364. CIRMi353-A (CW70118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1365. CIRMi354-A (CW70120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1366. CIRMi355-A (CW70122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1367. CIRMi356-A (CW70123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1368. CIRMi357-A (CW70124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1369. CIRMi358-A (CW70125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1370. CIRMi359-A (CW70127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1371. CIRMi360-A (CW70128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1372. CIRMi361-A (CW70129)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1373. CIRMi362-A (CW70130)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1374. CIRMi363-A (CW70131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1375. CIRMi364-A (CW70132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1376. CIRMi365-A (CW70133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1377. CIRMi366-A (CW70134)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1378. CIRMi367-A (CW70135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1379. CIRMi368-A (CW70137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1380. CIRMi369-A (CW70138)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1381. CIRMi370-A (CW70140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1382. CIRMi371-A (CW70141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1383. CIRMi372-A (CW70142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1384. CIRMi373-A (CW70143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1385. CIRMi374-A (CW70144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1386. CIRMi375-A (CW70151)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1387. CIRMi376-A (CW70152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1388. CIRMi377-A (CW70155)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1389. CIRMi378-A (CW70156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1390. CIRMi379-A (CW70158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1391. CIRMi380-A (CW70160)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1392. CIRMi381-A (CW70161)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1393. CIRMi382-A (CW70164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1394. CIRMi383-A (CW70165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1395. CIRMi384-A (CW70167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1396. CIRMi385-A (CW70168)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1397. CIRMi386-A (CW70170)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1398. CIRMi387-A (CW70171)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1399. CIRMi388-A (CW70172)

    United States California Institute for Regenerative Medicine (CIRM)

  1400. CIRMi389-A (CW70173)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1401. CIRMi390-A (CW70174)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1402. CIRMi391-A (CW70175)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1403. CIRMi392-A (CW70176)

    United States California Institute for Regenerative Medicine (CIRM)

  1404. CIRMi393-A (CW70177)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1405. CIRMi394-A (CW70179)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1406. CIRMi395-A (CW70181)

    United States California Institute for Regenerative Medicine (CIRM)

  1407. CIRMi396-A (CW70182)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1408. CIRMi397-A (CW70010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1409. CIRMi398-A (CW70054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1410. CIRMi399-A (CW70055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1411. CIRMi400-A (CW70080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1412. CIRMi401-A (CW70184)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1413. CIRMi402-A (CW70185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1414. CIRMi403-A (CW70186)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1415. CIRMi404-A (CW70188)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1416. CIRMi405-A (CW70189)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1417. CIRMi406-A (CW70190)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1418. CIRMi407-A (CW70191)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinal detachment

  1419. CIRMi408-A (CW70193)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1420. CIRMi409-A (CW70194)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1421. CIRMi410-A (CW70195)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1422. CIRMi411-A (CW70196)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1423. CIRMi412-A (CW70197)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1424. CIRMi413-A (CW70198)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1425. CIRMi414-A (CW70201)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1426. CIRMi415-A (CW70203)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1427. CIRMi416-A (CW70205)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1428. CIRMi417-A (CW70206)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1429. CIRMi418-A (CW70207)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1430. CIRMi419-A (CW70208)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1431. CIRMi420-A (CW70210)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1432. CIRMi421-A (CW70211)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1433. CIRMi422-A (CW70212)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1434. CIRMi423-A (CW70213)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1435. CIRMi424-A (CW70214)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1436. CIRMi425-A (CW70215)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1437. CIRMi426-A (CW70216)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1438. CIRMi427-A (CW70217)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1439. CIRMi428-A (CW70219)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1440. CIRMi429-A (CW70221)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1441. CIRMi430-A (CW70224)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1442. CIRMi431-A (CW70225)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1443. CIRMi432-A (CW70226)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1444. CIRMi433-A (CW70229)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1445. CIRMi434-A (CW70230)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1446. CIRMi435-A (CW70232)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1447. CIRMi436-A (CW70233)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1448. CIRMi437-A (CW70235)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1449. CIRMi438-A (CW70239)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1450. CIRMi439-A (CW70240)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1451. CIRMi440-A (CW70241)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1452. CIRMi441-A (CW70244)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1453. CIRMi442-A (CW70245)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1454. CIRMi443-A (CW70246)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1455. CIRMi444-A (CW70247)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1456. CIRMi445-A (CW70248)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1457. CIRMi446-A (CW70249)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1458. CIRMi447-A (CW70250)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1459. CIRMi448-A (CW70251)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1460. CIRMi449-A (CW70252)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1461. CIRMi450-A (CW70253)

    United States California Institute for Regenerative Medicine (CIRM)

  1462. CIRMi451-A (CW70254)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1463. CIRMi452-A (CW70255)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1464. CIRMi453-A (CW70256)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1465. CIRMi454-A (CW70257)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1466. CIRMi455-A (CW70258)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1467. CIRMi456-A (CW70259)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1468. CIRMi457-A (CW70260)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1469. CIRMi458-A (CW70261)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1470. CIRMi459-A (CW70262)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1471. CIRMi460-A (CW70263)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1472. CIRMi461-A (CW70264)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1473. CIRMi462-A (CW70265)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1474. CIRMi463-A (CW70266)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1475. CIRMi464-A (CW70267)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1476. CIRMi465-A (CW70269)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1477. CIRMi466-A (CW70270)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1478. CIRMi467-A (CW70272)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1479. CIRMi468-A (CW70273)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1480. CIRMi469-A (CW70274)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1481. CIRMi470-A (CW70275)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1482. CIRMi471-A (CW70276)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1483. CIRMi472-A (CW70278)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1484. CIRMi473-A (CW70279)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1485. CIRMi474-A (CW70280)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1486. CIRMi475-A (CW70281)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1487. CIRMi476-A (CW70282)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1488. CIRMi477-A (CW70283)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1489. CIRMi478-A (CW70284)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1490. CIRMi479-A (CW70286)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1491. CIRMi480-A (CW70287)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1492. CIRMi481-A (CW70289)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1493. CIRMi482-A (CW70290)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1494. CIRMi483-A (CW70292)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1495. CIRMi484-A (CW70296)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1496. CIRMi485-A (CW70297)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1497. CIRMi486-A (CW70298)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1498. CIRMi487-A (CW70299)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1499. CIRMi488-A (CW70300)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Achromatopsia

  1500. CIRMi489-A (CW70301)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1501. CIRMi490-A (CW70303)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1502. CIRMi491-A (CW70304)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1503. CIRMi492-A (CW70305)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1504. CIRMi493-A (CW70306)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1505. CIRMi494-A (CW70307)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1506. CIRMi495-A (CW70308)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1507. CIRMi496-A (CW70309)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1508. CIRMi497-A (CW70310)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1509. CIRMi498-A (CW70313)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1510. CIRMi499-A (CW70314)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1511. CIRMi500-A (CW70315)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1512. CIRMi501-A (CW70316)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1513. CIRMi502-A (CW70317)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1514. CIRMi503-A (CW70318)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1515. CIRMi504-A (CW70319)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Doyne honeycomb retinal dystrophy

  1516. CIRMi505-A (CW70320)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1517. CIRMi506-A (CW70321)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1518. CIRMi507-A (CW70322)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1519. CIRMi508-A (CW70323)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinitis pigmentosa

  1520. CIRMi509-A (CW70324)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1521. CIRMi510-A (CW70325)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1522. CIRMi511-A (CW70326)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1523. CIRMi512-A (CW70327)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1524. CIRMi513-A (CW70330)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1525. CIRMi514-A (CW70332)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1526. CIRMi515-A (CW70337)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1527. CIRMi516-A (CW70338)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1528. CIRMi517-A (CW70339)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cataract

  1529. CIRMi518-A (CW70341)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1530. CIRMi519-A (CW70342)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinitis pigmentosa

  1531. CIRMi520-A (CW70343)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1532. CIRMi521-A (CW70344)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1533. CIRMi522-A (CW70345)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1534. CIRMi523-A (CW70346)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1535. CIRMi524-A (CW70347)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1536. CIRMi525-A (CW70348)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinitis pigmentosa

  1537. CIRMi526-A (CW70350)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1538. CIRMi527-A (CW70351)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1539. CIRMi528-A (CW70353)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1540. CIRMi529-A (CW70354)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1541. CIRMi530-A (CW70355)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1542. CIRMi531-A (CW70356)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinitis pigmentosa

  1543. CIRMi532-A (CW70358)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1544. CIRMi533-A (CW70359)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1545. CIRMi534-A (CW70363)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1546. CIRMi535-A (CW70364)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1547. CIRMi536-A (CW70366)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1548. CIRMi537-A (CW70368)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1549. CIRMi538-A (CW70369)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1550. CIRMi539-A (CW70370)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1551. CIRMi540-A (CW70371)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1552. CIRMi541-A (CW70372)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1553. CIRMi542-A (CW70373)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinitis pigmentosa

  1554. CIRMi543-A (CW70384)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1555. CIRMi544-A (CW40002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1556. CIRMi545-A (CW40003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1557. CIRMi546-A (CW40004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1558. CIRMi547-A (CW40005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1559. CIRMi548-A (CW40006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1560. CIRMi549-A (CW40009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1561. CIRMi550-A (CW40010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1562. CIRMi551-A (CW40011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1563. CIRMi552-A (CW40012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1564. CIRMi553-A (CW40013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1565. CIRMi554-A (CW40014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1566. CIRMi555-A (CW40015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1567. CIRMi556-A (CW40017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1568. CIRMi557-A (CW40018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1569. CIRMi558-A (CW40020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1570. CIRMi559-A (CW40021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1571. CIRMi560-A (CW40022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1572. CIRMi561-A (CW40023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1573. CIRMi562-A (CW40024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1574. CIRMi563-A (CW40025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1575. CIRMi564-A (CW40026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1576. CIRMi565-A (CW40027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1577. CIRMi566-A (CW40028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1578. CIRMi567-A (CW40029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1579. CIRMi568-A (CW40030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1580. CIRMi569-A (CW40031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1581. CIRMi570-A (CW40032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1582. CIRMi571-A (CW40033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1583. CIRMi572-A (CW40034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1584. CIRMi573-A (CW40035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1585. CIRMi574-A (CW40037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1586. CIRMi575-A (CW40038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1587. CIRMi576-A (CW40039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1588. CIRMi577-A (CW40040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1589. CIRMi578-A (CW40042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1590. CIRMi579-A (CW40043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1591. CIRMi580-A (CW40044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1592. CIRMi581-A (CW40046)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1593. CIRMi582-A (CW40047)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1594. CIRMi583-A (CW40049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1595. CIRMi584-A (CW40051)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1596. CIRMi585-A (CW40052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1597. CIRMi586-A (CW40053)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1598. CIRMi587-A (CW40054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1599. CIRMi588-A (CW40055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1600. CIRMi589-A (CW40057)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1601. CIRMi590-A (CW40061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1602. CIRMi591-A (CW40062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1603. CIRMi592-A (CW40063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1604. CIRMi593-A (CW40064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1605. CIRMi594-A (CW40065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1606. CIRMi595-A (CW40066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1607. CIRMi596-A (CW40067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1608. CIRMi597-A (CW40068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1609. CIRMi598-A (CW40070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1610. CIRMi599-A (CW40071)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1611. CIRMi600-A (CW40073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1612. CIRMi601-A (CW40074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1613. CIRMi602-A (CW40075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1614. CIRMi603-A (CW40077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1615. CIRMi604-A (CW40078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1616. CIRMi605-A (CW40079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1617. CIRMi606-A (CW40080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1618. CIRMi607-A (CW40081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1619. CIRMi608-A (CW40083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1620. CIRMi609-A (CW40084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1621. CIRMi610-A (CW40085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1622. CIRMi611-A (CW40086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1623. CIRMi612-A (CW40087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1624. CIRMi613-A (CW40088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1625. CIRMi614-A (CW40089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1626. CIRMi615-A (CW40090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1627. CIRMi616-A (CW40091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1628. CIRMi617-A (CW40092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1629. CIRMi618-A (CW40094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1630. CIRMi619-A (CW40096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1631. CIRMi620-A (CW40097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1632. CIRMi621-A (CW40100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1633. CIRMi622-A (CW40101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1634. CIRMi623-A (CW40105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1635. CIRMi624-A (CW40106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1636. CIRMi625-A (CW40107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1637. CIRMi626-A (CW40109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1638. CIRMi627-A (CW40110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1639. CIRMi628-A (CW40111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1640. CIRMi629-A (CW40112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1641. CIRMi630-A (CW40113)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1642. CIRMi631-A (CW40114)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1643. CIRMi632-A (CW40115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1644. CIRMi633-A (CW40116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1645. CIRMi634-A (CW40118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1646. CIRMi635-A (CW40119)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1647. CIRMi636-A (CW40120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1648. CIRMi637-A (CW40121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1649. CIRMi638-A (CW40122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1650. CIRMi639-A (CW40123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1651. CIRMi640-A (CW40124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1652. CIRMi641-A (CW40125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1653. CIRMi642-A (CW40126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1654. CIRMi643-A (CW40127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1655. CIRMi644-A (CW40128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1656. CIRMi645-A (CW40129)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1657. CIRMi646-A (CW40131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1658. CIRMi647-A (CW40132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1659. CIRMi648-A (CW40135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1660. CIRMi649-A (CW40136)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1661. CIRMi650-A (CW40137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1662. CIRMi651-A (CW40139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1663. CIRMi652-A (CW40142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1664. CIRMi653-A (CW40144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1665. CIRMi654-A (CW40145)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1666. CIRMi655-A (CW40147)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1667. CIRMi656-A (CW40148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1668. CIRMi657-A (CW40149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1669. CIRMi658-A (CW40152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1670. CIRMi659-A (CW40153)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1671. CIRMi660-A (CW40157)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1672. CIRMi661-A (CW40159)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1673. CIRMi662-A (CW40160)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1674. CIRMi663-A (CW40161)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1675. CIRMi664-A (CW40163)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1676. CIRMi665-A (CW40164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1677. CIRMi666-A (CW40165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1678. CIRMi667-A (CW40167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1679. CIRMi668-A (CW40169)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1680. CIRMi669-A (CW40172)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1681. CIRMi670-A (CW40174)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1682. CIRMi671-A (CW40178)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1683. CIRMi672-A (CW40181)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1684. CIRMi673-A (CW40182)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1685. CIRMi674-A (CW40183)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1686. CIRMi675-A (CW40185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1687. CIRMi676-A (CW40187)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1688. CIRMi677-A (CW40190)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1689. CIRMi678-A (CW40191)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1690. CIRMi679-A (CW40192)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1691. CIRMi680-A (CW40193)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1692. CIRMi681-A (CW40194)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1693. CIRMi682-A (CW40195)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1694. CIRMi683-A (CW40196)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1695. CIRMi684-A (CW40197)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1696. CIRMi685-A (CW40198)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1697. CIRMi686-A (CW40199)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1698. CIRMi687-A (CW40200)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1699. CIRMi688-A (CW40201)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1700. CIRMi689-A (CW40206)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1701. CIRMi690-A (CW40207)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1702. CIRMi691-A (CW40208)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1703. CIRMi692-A (CW40209)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1704. CIRMi693-A (CW40211)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1705. CIRMi694-A (CW40212)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1706. CIRMi695-A (CW40213)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1707. CIRMi696-A (CW40214)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1708. CIRMi697-A (CW40217)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1709. CIRMi698-A (CW40218)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1710. CIRMi699-A (CW40219)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1711. CIRMi700-A (CW40220)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1712. CIRMi701-A (CW40221)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1713. CIRMi702-A (CW40222)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1714. CIRMi703-A (CW40224)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1715. CIRMi704-A (CW40225)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1716. CIRMi705-A (CW40226)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1717. CIRMi706-A (CW40227)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1718. CIRMi707-A (CW40228)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1719. CIRMi708-A (CW40229)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1720. CIRMi709-A (CW40230)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1721. CIRMi710-A (CW40231)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1722. CIRMi711-A (CW40232)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1723. CIRMi712-A (CW40233)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1724. CIRMi713-A (CW40234)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1725. CIRMi714-A (CW40235)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1726. CIRMi715-A (CW40236)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1727. CIRMi716-A (CW40237)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1728. CIRMi717-A (CW40239)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1729. CIRMi718-A (CW40243)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1730. CIRMi719-A (CW40244)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1731. CIRMi720-A (CW40245)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1732. CIRMi721-A (CW40246)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1733. CIRMi722-A (CW40247)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1734. CIRMi723-A (CW40249)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1735. CIRMi724-A (CW40250)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1736. CIRMi725-A (CW40251)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1737. CIRMi726-A (CW30001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1738. CIRMi727-A (CW30002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1739. CIRMi728-A (CW30003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1740. CIRMi729-A (CW30004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1741. CIRMi730-A (CW30005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1742. CIRMi731-A (CW30006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1743. CIRMi732-A (CW30007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1744. CIRMi733-A (CW30008)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1745. CIRMi734-A (CW30009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1746. CIRMi735-A (CW30010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1747. CIRMi736-A (CW30011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1748. CIRMi737-A (CW30012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1749. CIRMi738-A (CW30014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1750. CIRMi739-A (CW30015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1751. CIRMi740-A (CW30016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1752. CIRMi741-A (CW30017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1753. CIRMi742-A (CW30018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1754. CIRMi743-A (CW30019)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1755. CIRMi744-A (CW30020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1756. CIRMi745-A (CW30022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1757. CIRMi746-A (CW30024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1758. CIRMi747-A (CW30027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1759. CIRMi748-A (CW30028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1760. CIRMi749-A (CW30029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1761. CIRMi750-A (CW30030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1762. CIRMi751-A (CW30031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1763. CIRMi752-A (CW30032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1764. CIRMi753-A (CW30033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1765. CIRMi754-A (CW30035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1766. CIRMi755-A (CW30036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1767. CIRMi756-A (CW30037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1768. CIRMi757-A (CW30038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1769. CIRMi758-A (CW30040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1770. CIRMi759-A (CW30042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1771. CIRMi760-A (CW30043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1772. CIRMi761-A (CW30044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1773. CIRMi762-A (CW30045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1774. CIRMi763-A (CW30046)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1775. CIRMi764-A (CW30048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1776. CIRMi765-A (CW30049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1777. CIRMi766-A (CW30050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1778. CIRMi767-A (CW30051)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1779. CIRMi768-A (CW30052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1780. CIRMi769-A (CW30053)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1781. CIRMi770-A (CW30054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1782. CIRMi771-A (CW30055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1783. CIRMi772-A (CW30056)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1784. CIRMi773-A (CW30058)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1785. CIRMi774-A (CW30059)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1786. CIRMi775-A (CW30060)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1787. CIRMi776-A (CW30061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1788. CIRMi777-A (CW30062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1789. CIRMi778-A (CW30063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1790. CIRMi779-A (CW30064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1791. CIRMi780-A (CW30065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1792. CIRMi781-A (CW30067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1793. CIRMi782-A (CW30068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1794. CIRMi783-A (CW30069)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1795. CIRMi784-A (CW30070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1796. CIRMi785-A (CW30071)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1797. CIRMi786-A (CW30073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1798. CIRMi787-A (CW30074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1799. CIRMi788-A (CW30075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1800. CIRMi789-A (CW30076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1801. CIRMi790-A (CW30077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1802. CIRMi791-A (CW30078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1803. CIRMi792-A (CW30079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1804. CIRMi793-A (CW30080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1805. CIRMi794-A (CW30081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1806. CIRMi795-A (CW30082)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1807. CIRMi796-A (CW30083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1808. CIRMi797-A (CW30084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1809. CIRMi798-A (CW30085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1810. CIRMi799-A (CW30086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1811. CIRMi800-A (CW30089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1812. CIRMi801-A (CW30090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1813. CIRMi802-A (CW30092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1814. CIRMi803-A (CW30093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  1815. CIRMi804-A (CW30094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1816. CIRMi805-A (CW30095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1817. CIRMi806-A (CW30096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1818. CIRMi807-A (CW30097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1819. CIRMi808-A (CW30098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1820. CIRMi809-A (CW30099)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1821. CIRMi810-A (CW30101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1822. CIRMi811-A (CW30102)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1823. CIRMi812-A (CW30103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1824. CIRMi813-A (CW30104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1825. CIRMi814-A (CW30105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1826. CIRMi815-A (CW30106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1827. CIRMi816-A (CW30107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1828. CIRMi817-A (CW30108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1829. CIRMi818-A (CW30109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1830. CIRMi819-A (CW30110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1831. CIRMi820-A (CW30111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1832. CIRMi821-A (CW30112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1833. CIRMi822-A (CW30113)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1834. CIRMi823-A (CW30115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1835. CIRMi824-A (CW30116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1836. CIRMi825-A (CW30119)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1837. CIRMi826-A (CW30120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1838. CIRMi827-A (CW30121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1839. CIRMi828-A (CW30122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1840. CIRMi829-A (CW30125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1841. CIRMi830-A (CW30126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1842. CIRMi831-A (CW30128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1843. CIRMi832-A (CW30130)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1844. CIRMi833-A (CW30131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1845. CIRMi834-A (CW30132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1846. CIRMi835-A (CW30133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1847. CIRMi836-A (CW30137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1848. CIRMi837-A (CW30138)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1849. CIRMi838-A (CW30139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1850. CIRMi839-A (CW30140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1851. CIRMi840-A (CW30141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1852. CIRMi841-A (CW30142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1853. CIRMi842-A (CW30143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1854. CIRMi843-A (CW30145)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1855. CIRMi844-A (CW30146)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1856. CIRMi845-A (CW30148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1857. CIRMi846-A (CW30149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  1858. CIRMi847-A (CW30151)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1859. CIRMi848-A (CW30152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1860. CIRMi849-A (CW30154)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1861. CIRMi850-A (CW30155)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1862. CIRMi851-A (CW30156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1863. CIRMi852-A (CW30157)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1864. CIRMi853-A (CW30158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1865. CIRMi854-A (CW30159)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1866. CIRMi855-A (CW30161)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1867. CIRMi856-A (CW30163)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1868. CIRMi857-A (CW30164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1869. CIRMi858-A (CW30165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1870. CIRMi859-A (CW30166)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1871. CIRMi860-A (CW30167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1872. CIRMi861-A (CW30168)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1873. CIRMi862-A (CW30169)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1874. CIRMi863-A (CW30170)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1875. CIRMi864-A (CW30171)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1876. CIRMi865-A (CW30172)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1877. CIRMi866-A (CW30174)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1878. CIRMi867-A (CW30175)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1879. CIRMi868-A (CW30176)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1880. CIRMi869-A (CW30177)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1881. CIRMi870-A (CW30178)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1882. CIRMi871-A (CW30179)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1883. CIRMi872-A (CW30180)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1884. CIRMi873-A (CW30181)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1885. CIRMi874-A (CW30182)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1886. CIRMi875-A (CW30184)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1887. CIRMi876-A (CW30185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1888. CIRMi877-A (CW30188)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1889. CIRMi878-A (CW30189)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1890. CIRMi879-A (CW30190)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1891. CIRMi880-A (CW30191)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1892. CIRMi881-A (CW30192)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1893. CIRMi882-A (CW30193)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1894. CIRMi883-A (CW30194)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1895. CIRMi884-A (CW30195)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1896. CIRMi885-A (CW30196)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1897. CIRMi886-A (CW30197)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1898. CIRMi887-A (CW30198)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1899. CIRMi888-A (CW30199)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1900. CIRMi889-A (CW30200)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1901. CIRMi890-A (CW30202)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1902. CIRMi891-A (CW30203)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1903. CIRMi892-A (CW30204)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1904. CIRMi893-A (CW30205)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1905. CIRMi894-A (CW30207)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1906. CIRMi895-A (CW30208)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1907. CIRMi896-A (CW30209)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1908. CIRMi897-A (CW30210)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  1909. CIRMi898-A (CW30211)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1910. CIRMi899-A (CW30212)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1911. CIRMi900-A (CW30213)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1912. CIRMi901-A (CW30214)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1913. CIRMi902-A (CW30215)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1914. CIRMi903-A (CW30216)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1915. CIRMi904-A (CW30219)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1916. CIRMi905-A (CW30220)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1917. CIRMi906-A (CW30221)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1918. CIRMi907-A (CW30222)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1919. CIRMi908-A (CW30223)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1920. CIRMi909-A (CW30224)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1921. CIRMi910-A (CW30225)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  1922. CIRMi911-A (CW30226)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1923. CIRMi912-A (CW30227)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1924. CIRMi913-A (CW30228)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1925. CIRMi914-A (CW30229)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1926. CIRMi915-A (CW30230)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1927. CIRMi916-A (CW30231)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1928. CIRMi917-A (CW30232)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1929. CIRMi918-A (CW30233)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1930. CIRMi919-A (CW30234)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1931. CIRMi920-A (CW30235)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1932. CIRMi921-A (CW30236)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1933. CIRMi922-A (CW30237)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1934. CIRMi923-A (CW30238)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1935. CIRMi924-A (CW30240)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1936. CIRMi925-A (CW30241)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1937. CIRMi926-A (CW30242)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1938. CIRMi927-A (CW30243)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1939. CIRMi928-A (CW30244)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1940. CIRMi929-A (CW30245)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1941. CIRMi930-A (CW30246)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1942. CIRMi931-A (CW30247)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1943. CIRMi932-A (CW30248)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1944. CIRMi933-A (CW30249)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1945. CIRMi934-A (CW30251)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1946. CIRMi935-A (CW30253)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1947. CIRMi936-A (CW30254)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1948. CIRMi937-A (CW30256)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1949. CIRMi938-A (CW30257)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1950. CIRMi939-A (CW30258)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1951. CIRMi940-A (CW30259)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1952. CIRMi941-A (CW30260)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1953. CIRMi942-A (CW30261)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1954. CIRMi943-A (CW30262)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1955. CIRMi944-A (CW30263)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1956. CIRMi945-A (CW30264)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1957. CIRMi946-A (CW30265)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1958. CIRMi947-A (CW30266)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1959. CIRMi948-A (CW30267)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1960. CIRMi949-A (CW30268)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1961. CIRMi950-A (CW30269)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1962. CIRMi951-A (CW30270)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1963. CIRMi952-A (CW30272)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1964. CIRMi953-A (CW30273)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1965. CIRMi954-A (CW30274)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1966. CIRMi955-A (CW30275)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1967. CIRMi956-A (CW30276)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1968. CIRMi957-A (CW30279)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1969. CIRMi958-A (CW30280)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1970. CIRMi959-A (CW30282)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1971. CIRMi960-A (CW30283)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1972. CIRMi961-A (CW30284)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1973. CIRMi962-A (CW30285)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1974. CIRMi963-A (CW30286)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1975. CIRMi964-A (CW30287)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1976. CIRMi965-A (CW30288)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1977. CIRMi966-A (CW30289)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Arrhythmogenic right ventricular dysplasia

  1978. CIRMi967-A (CW30290)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1979. CIRMi968-A (CW30291)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1980. CIRMi969-A (CW30292)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1981. CIRMi970-A (CW30293)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1982. CIRMi971-A (CW30295)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1983. CIRMi972-A (CW30297)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1984. CIRMi973-A (CW30298)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1985. CIRMi974-A (CW30299)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1986. CIRMi975-A (CW30300)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1987. CIRMi976-A (CW30302)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1988. CIRMi977-A (CW30303)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1989. CIRMi978-A (CW30305)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1990. CIRMi979-A (CW30306)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1991. CIRMi980-A (CW30307)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1992. CIRMi981-A (CW30309)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1993. CIRMi982-A (CW30310)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1994. CIRMi983-A (CW30311)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1995. CIRMi984-A (CW30312)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1996. CIRMi985-A (CW30314)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1997. CIRMi986-A (CW30316)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1998. CIRMi987-A (CW30317)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1999. CIRMi988-A (CW30318)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2000. CIRMi989-A (CW30319)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2001. CIRMi990-A (CW30320)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2002. CIRMi991-A (CW30321)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2003. CIRMi992-A (CW30322)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2004. CIRMi993-A (CW30323)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2005. CIRMi994-A (CW30324)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2006. CIRMi995-A (CW30325)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2007. CIRMi996-A (CW30326)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2008. CIRMi997-A (CW30327)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2009. CIRMi998-A (CW30328)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2010. CIRMi999-A (CW30329)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2011. CIRMi00A-A (CW30331)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2012. CIRMi00B-A (CW30332)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2013. CIRMi00C-A (CW30333)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2014. CIRMi00D-A (CW30334)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2015. CIRMi00E-A (CW30335)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2016. CIRMi00F-A (CW30336)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2017. CIRMi00G-A (CW30337)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2018. CIRMi00H-A (CW30338)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2019. CIRMi00I-A (CW30339)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2020. CIRMi00J-A (CW30340)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2021. CIRMi00K-A (CW30342)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2022. CIRMi00L-A (CW30343)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2023. CIRMi00M-A (CW30344)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2024. CIRMi00N-A (CW30345)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2025. CIRMi00O-A (CW30346)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2026. CIRMi00P-A (CW30348)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2027. CIRMi00Q-A (CW30349)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2028. CIRMi00R-A (CW30350)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2029. CIRMi00S-A (CW30353)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2030. CIRMi00T-A (CW30354)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2031. CIRMi00U-A (CW30355)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2032. CIRMi00V-A (CW30356)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2033. CIRMi00W-A (CW30357)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2034. CIRMi00X-A (CW30358)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2035. CIRMi00Y-A (CW30359)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  2036. CIRMi00Z-A (CW30360)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2037. CIRMi01A-A (CW30361)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2038. CIRMi01B-A (CW30362)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2039. CIRMi01C-A (CW30363)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2040. CIRMi01D-A (CW30364)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2041. CIRMi01E-A (CW30369)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2042. CIRMi01F-A (CW30370)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2043. CIRMi01G-A (CW30371)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2044. CIRMi01H-A (CW30374)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2045. CIRMi01I-A (CW30376)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2046. CIRMi01J-A (CW30380)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2047. CIRMi01K-A (CW30382)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2048. CIRMi01L-A (CW30383)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2049. CIRMi01M-A (CW30386)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2050. CIRMi01N-A (CW30387)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2051. CIRMi01O-A (CW30389)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2052. CIRMi01P-A (CW30390)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2053. CIRMi01Q-A (CW30391)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2054. CIRMi01R-A (CW30392)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2055. CIRMi01S-A (CW30393)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2056. CIRMi01T-A (CW30394)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2057. CIRMi01U-A (CW30395)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2058. CIRMi01V-A (CW30397)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2059. CIRMi01W-A (CW30398)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2060. CIRMi01X-A (CW30399)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2061. CIRMi01Y-A (CW30400)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2062. CIRMi01Z-A (CW30401)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2063. CIRMi02A-A (CW30403)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2064. CIRMi02B-A (CW30404)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2065. CIRMi02C-A (CW30406)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2066. CIRMi02D-A (CW30408)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2067. CIRMi02E-A (CW30409)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2068. CIRMi02F-A (CW30410)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2069. CIRMi02G-A (CW30412)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2070. CIRMi02H-A (CW30413)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2071. CIRMi02I-A (CW30414)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2072. CIRMi02J-A (CW30415)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2073. CIRMi02K-A (CW30417)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2074. CIRMi02L-A (CW30418)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2075. CIRMi02M-A (CW30419)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2076. CIRMi02N-A (CW30420)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2077. CIRMi02O-A (CW30421)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2078. CIRMi02P-A (CW30422)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2079. CIRMi02Q-A (CW30423)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2080. CIRMi02R-A (CW30425)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2081. CIRMi02S-A (CW30426)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2082. CIRMi02T-A (CW30427)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2083. CIRMi02U-A (CW30428)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2084. CIRMi02V-A (CW30429)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  2085. CIRMi02W-A (CW30430)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2086. CIRMi02X-A (CW30431)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2087. CIRMi02Y-A (CW30432)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2088. CIRMi02Z-A (CW30433)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Arrhythmogenic right ventricular dysplasia

  2089. CIRMi03A-A (CW30434)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2090. CIRMi03B-A (CW30435)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2091. CIRMi03C-A (CW30436)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2092. CIRMi03D-A (CW30437)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2093. CIRMi03E-A (CW30438)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2094. CIRMi03F-A (CW30439)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2095. CIRMi03G-A (CW30440)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2096. CIRMi03H-A (CW30441)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2097. CIRMi03I-A (CW30442)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2098. CIRMi03J-A (CW30443)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2099. CIRMi03K-A (CW30444)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2100. CIRMi03L-A (CW30445)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2101. CIRMi03M-A (CW30446)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2102. CIRMi03N-A (CW30447)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2103. CIRMi03O-A (CW30448)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2104. CIRMi03P-A (CW30449)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2105. CIRMi03Q-A (CW30450)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2106. CIRMi03R-A (CW30452)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2107. CIRMi03S-A (CW30453)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2108. CIRMi03T-A (CW30454)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2109. CIRMi03U-A (CW30455)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2110. CIRMi03V-A (CW30456)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2111. CIRMi03W-A (CW30457)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2112. CIRMi03X-A (CW30459)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2113. CIRMi03Y-A (CW30460)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2114. CIRMi03Z-A (CW30461)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2115. CIRMi04A-A (CW30462)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2116. CIRMi04B-A (CW30463)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2117. CIRMi04C-A (CW30464)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2118. CIRMi04D-A (CW30465)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2119. CIRMi04E-A (CW30466)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2120. CIRMi04F-A (CW30467)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2121. CIRMi04G-A (CW30468)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2122. CIRMi04H-A (CW30470)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2123. CIRMi04I-A (CW30471)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2124. CIRMi04J-A (CW30472)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2125. CIRMi04K-A (CW30473)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2126. CIRMi04L-A (CW30474)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2127. CIRMi04M-A (CW30476)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2128. CIRMi04N-A (CW30477)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2129. CIRMi04O-A (CW30478)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2130. CIRMi04P-A (CW30479)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2131. CIRMi04Q-A (CW30480)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2132. CIRMi04R-A (CW30481)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2133. CIRMi04S-A (CW30482)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2134. CIRMi04T-A (CW30483)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2135. CIRMi04U-A (CW30484)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Restrictive cardiomyopathy

  2136. CIRMi04V-A (CW30485)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  2137. CIRMi04W-A (CW30486)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2138. CIRMi04X-A (CW30488)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2139. CIRMi04Y-A (CW30489)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2140. CIRMi04Z-A (CW30490)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2141. CIRMi05A-A (CW30491)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2142. CIRMi05B-A (CW30492)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2143. CIRMi05C-A (CW30494)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2144. CIRMi05D-A (CW30495)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2145. CIRMi05E-A (CW30496)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2146. CIRMi05F-A (CW30497)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2147. CIRMi05G-A (CW30499)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2148. CIRMi05H-A (CW30500)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2149. CIRMi05I-A (CW30501)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2150. CIRMi05J-A (CW30503)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2151. CIRMi05K-A (CW30505)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2152. CIRMi05L-A (CW30506)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2153. CIRMi05M-A (CW30508)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2154. CIRMi05N-A (CW30509)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2155. CIRMi05O-A (CW30510)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2156. CIRMi05P-A (CW30512)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2157. CIRMi05Q-A (CW30513)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2158. CIRMi05R-A (CW30515)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2159. CIRMi05S-A (CW30516)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2160. CIRMi05T-A (CW30519)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2161. CIRMi05U-A (CW30520)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  2162. CIRMi05V-A (CW30522)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2163. CIRMi05W-A (CW30523)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2164. CIRMi05X-A (CW30525)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2165. CIRMi05Y-A (CW30526)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2166. CIRMi05Z-A (CW30527)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2167. CIRMi06A-A (CW30528)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2168. CIRMi06B-A (CW30529)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2169. CIRMi06C-A (CW10001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2170. CIRMi06D-A (CW10002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2171. CIRMi06E-A (CW10003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2172. CIRMi06F-A (CW10004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2173. CIRMi06G-A (CW10005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2174. CIRMi06H-A (CW10007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2175. CIRMi06I-A (CW10009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2176. CIRMi06J-A (CW10010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2177. CIRMi06K-A (CW10011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2178. CIRMi06L-A (CW10012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2179. CIRMi06M-A (CW10013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2180. CIRMi06N-A (CW10014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2181. CIRMi06O-A (CW10015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatic steatosis

  2182. CIRMi06P-A (CW10018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2183. CIRMi06Q-A (CW10020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2184. CIRMi06R-A (CW10021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2185. CIRMi06S-A (CW10023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2186. CIRMi06T-A (CW10024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2187. CIRMi06U-A (CW10025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2188. CIRMi06V-A (CW10026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2189. CIRMi06W-A (CW10027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2190. CIRMi06X-A (CW10030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2191. CIRMi06Y-A (CW10033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2192. CIRMi06Z-A (CW10034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2193. CIRMi07A-A (CW10035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2194. CIRMi07B-A (CW10036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2195. CIRMi07C-A (CW10037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2196. CIRMi07D-A (CW10038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2197. CIRMi07E-A (CW10039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2198. CIRMi07F-A (CW10040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2199. CIRMi07G-A (CW10041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2200. CIRMi07H-A (CW10042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2201. CIRMi07I-A (CW10044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2202. CIRMi07J-A (CW10045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2203. CIRMi07K-A (CW10050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2204. CIRMi07L-A (CW10054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2205. CIRMi07M-A (CW10058)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2206. CIRMi07N-A (CW10060)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2207. CIRMi07O-A (CW10061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2208. CIRMi07P-A (CW10062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2209. CIRMi07Q-A (CW10063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2210. CIRMi07R-A (CW10064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2211. CIRMi07S-A (CW10066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2212. CIRMi07T-A (CW10067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2213. CIRMi07U-A (CW10068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2214. CIRMi07V-A (CW10069)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2215. CIRMi07W-A (CW10073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2216. CIRMi07X-A (CW10074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2217. CIRMi07Y-A (CW10075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2218. CIRMi07Z-A (CW10076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2219. CIRMi08A-A (CW10077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2220. CIRMi08B-A (CW10078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2221. CIRMi08C-A (CW10079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2222. CIRMi08D-A (CW10081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2223. CIRMi08E-A (CW10083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2224. CIRMi08F-A (CW10084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2225. CIRMi08G-A (CW10085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2226. CIRMi08H-A (CW10086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2227. CIRMi08I-A (CW10087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2228. CIRMi08J-A (CW10088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2229. CIRMi08K-A (CW10089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2230. CIRMi08L-A (CW10090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2231. CIRMi08M-A (CW10091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2232. CIRMi08N-A (CW10093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2233. CIRMi08O-A (CW10094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2234. CIRMi08P-A (CW10095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2235. CIRMi08Q-A (CW10096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2236. CIRMi08R-A (CW10097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2237. CIRMi08S-A (CW10098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2238. CIRMi08T-A (CW10100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2239. CIRMi08U-A (CW10101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2240. CIRMi08V-A (CW10102)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2241. CIRMi08W-A (CW10103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2242. CIRMi08X-A (CW10104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2243. CIRMi08Y-A (CW10107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2244. CIRMi08Z-A (CW10109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2245. CIRMi09A-A (CW10110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2246. CIRMi09B-A (CW10111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2247. CIRMi09C-A (CW10114)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2248. CIRMi09D-A (CW10115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2249. CIRMi09E-A (CW10116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2250. CIRMi09F-A (CW10118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2251. CIRMi09G-A (CW10120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2252. CIRMi09H-A (CW10121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2253. CIRMi09I-A (CW10122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2254. CIRMi09J-A (CW10126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2255. CIRMi09K-A (CW10127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2256. CIRMi09L-A (CW10128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2257. CIRMi09M-A (CW10130)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2258. CIRMi09N-A (CW10131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2259. CIRMi09O-A (CW10133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2260. CIRMi09P-A (CW10135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2261. CIRMi09Q-A (CW10136)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2262. CIRMi09R-A (CW10137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2263. CIRMi09S-A (CW10139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2264. CIRMi09T-A (CW10141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2265. CIRMi09U-A (CW10142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2266. CIRMi09V-A (CW10143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2267. CIRMi09W-A (CW10144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2268. CIRMi09X-A (CW10146)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2269. CIRMi09Y-A (CW10147)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2270. CIRMi09Z-A (CW10148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2271. CIRMi10A-A (CW10149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2272. CIRMi10B-A (CW10150)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2273. CIRMi10C-A (CW10152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2274. CIRMi10D-A (CW10153)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2275. CIRMi10E-A (CW10154)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2276. CIRMi10F-A (CW10155)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2277. CIRMi10G-A (CW10156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2278. CIRMi10H-A (CW10157)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2279. CIRMi10I-A (CW10158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2280. CIRMi10J-A (CW10159)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2281. CIRMi10K-A (CW10160)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2282. CIRMi10L-A (CW10162)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2283. CIRMi10M-A (CW10163)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2284. CIRMi10N-A (CW10165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2285. CIRMi10O-A (CW10166)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2286. CIRMi10P-A (CW10167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2287. CIRMi10Q-A (CW10168)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2288. CIRMi10R-A (CW10169)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2289. CIRMi10S-A (CW10171)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2290. CIRMi10T-A (CW10172)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2291. CIRMi10U-A (CW10173)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2292. CIRMi10V-A (CW10175)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2293. CIRMi10W-A (CW10176)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2294. CIRMi10X-A (CW10177)

    United States California Institute for Regenerative Medicine (CIRM)

  2295. CIRMi10Y-A (CW10178)

    United States California Institute for Regenerative Medicine (CIRM)

  2296. CIRMi10Z-A (CW10181)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2297. CIRMi11A-A (CW10182)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2298. CIRMi11B-A (CW10183)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2299. CIRMi11C-A (CW10184)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatic steatosis

  2300. CIRMi11D-A (CW10185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2301. CIRMi11E-A (CW10186)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2302. CIRMi11F-A (CW10187)

    United States California Institute for Regenerative Medicine (CIRM)

  2303. CIRMi11G-A (CW10188)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2304. CIRMi11H-A (CW10189)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2305. CIRMi11I-A (CW10190)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2306. CIRMi11J-A (CW10191)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2307. CIRMi11K-A (CW10192)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2308. CIRMi11L-A (CW10201)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2309. CIRMi11M-A (CW10202)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2310. CIRMi11N-A (CW10203)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2311. CIRMi11O-A (CW10205)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2312. CIRMi11P-A (CW10206)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2313. CIRMi11Q-A (CW10208)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2314. CIRMi11R-A (CW60314)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2315. CIRMi11S-A (CW60441)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2316. CIRMi11T-A (CW60520)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2317. CIRMi11U-A (CW11000)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2318. CIRMi11V-A (CW11001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2319. CIRMi11W-A (CW11004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2320. CIRMi11X-A (CW11005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2321. CIRMi11Y-A (CW11006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2322. CIRMi11Z-A (CW11009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2323. CIRMi12A-A (CW11012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2324. CIRMi12B-A (CW11013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2325. CIRMi12C-A (CW11015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2326. CIRMi12D-A (CW11016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2327. CIRMi12E-A (CW11018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2328. CIRMi12F-A (CW11019)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2329. CIRMi12G-A (CW11030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2330. CIRMi12H-A (CW11031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2331. CIRMi12I-A (CW11032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2332. CIRMi12J-A (CW11033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2333. CIRMi12K-A (CW11034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2334. CIRMi12L-A (CW11036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2335. CIRMi12M-A (CW11040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2336. CIRMi12N-A (CW11041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2337. CIRMi12O-A (CW11042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2338. CIRMi12P-A (CW11043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2339. CIRMi12Q-A (CW11046)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2340. CIRMi12R-A (CW11072)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2341. CIRMi12S-A (CW11074)

    United States California Institute for Regenerative Medicine (CIRM)

  2342. CIRMi12T-A (CW11075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2343. CIRMi12U-A (CW11077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2344. CIRMi12V-A (CW11078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2345. CIRMi12W-A (CW11079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2346. CIRMi12X-A (CW11090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2347. CIRMi12Y-A (CW11091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2348. CIRMi12Z-A (CW11093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2349. CIRMi13A-A (CW11094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2350. CIRMi13B-A (CW11096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2351. CIRMi13C-A (CW11098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2352. CIRMi13D-A (CW11100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2353. CIRMi13E-A (CW11101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2354. CIRMi13F-A (CW11110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2355. CIRMi13G-A (CW11119)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2356. CIRMi13H-A (CW11120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2357. CIRMi13I-A (CW11121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2358. CIRMi13J-A (CW11122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2359. CIRMi13K-A (CW11123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2360. CIRMi13L-A (CW11124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2361. CIRMi13M-A (CW11125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2362. CIRMi13N-A (CW11126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2363. CIRMi13O-A (CW11127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2364. CIRMi13P-A (CW11132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2365. CIRMi13Q-A (CW11133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2366. CIRMi13R-A (CW11140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2367. CIRMi13S-A (CW11141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2368. CIRMi13T-A (CW11147)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2369. CIRMi13U-A (CW11148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2370. CIRMi13V-A (CW11150)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2371. CIRMi13W-A (CW20001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2372. CIRMi13X-A (CW20002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2373. CIRMi13Y-A (CW20004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2374. CIRMi13Z-A (CW20006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2375. CIRMi14A-A (CW20008)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2376. CIRMi14B-A (CW20009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2377. CIRMi14C-A (CW20012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2378. CIRMi14D-A (CW20015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2379. CIRMi14E-A (CW20016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2380. CIRMi14F-A (CW20020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2381. CIRMi14G-A (CW20021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2382. CIRMi14H-A (CW20023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2383. CIRMi14I-A (CW20025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2384. CIRMi14J-A (CW20026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2385. CIRMi14K-A (CW20027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2386. CIRMi14L-A (CW20029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2387. CIRMi14M-A (CW20030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2388. CIRMi14N-A (CW20031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2389. CIRMi14O-A (CW20032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2390. CIRMi14P-A (CW20033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2391. CIRMi14Q-A (CW20034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2392. CIRMi14R-A (CW20035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2393. CIRMi14S-A (CW20039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2394. CIRMi14T-A (CW20041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2395. CIRMi14U-A (CW20042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2396. CIRMi14V-A (CW20043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2397. CIRMi14W-A (CW20044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2398. CIRMi14X-A (CW20046)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2399. CIRMi14Y-A (CW20047)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2400. CIRMi14Z-A (CW20048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2401. CIRMi15A-A (CW20049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2402. CIRMi15B-A (CW20050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2403. CIRMi15C-A (CW20051)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2404. CIRMi15D-A (CW20052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2405. CIRMi15E-A (CW20053)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2406. CIRMi15F-A (CW20054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2407. CIRMi15G-A (CW20055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2408. CIRMi15H-A (CW20056)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2409. CIRMi15I-A (CW20057)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2410. CIRMi15J-A (CW20058)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2411. CIRMi15K-A (CW20061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2412. CIRMi15L-A (CW20062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2413. CIRMi15M-A (CW20063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2414. CIRMi15N-A (CW20065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2415. CIRMi15O-A (CW20068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2416. CIRMi15P-A (CW20069)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2417. CIRMi15Q-A (CW20070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2418. CIRMi15R-A (CW20073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2419. CIRMi15S-A (CW20074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2420. CIRMi15T-A (CW20075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2421. CIRMi15U-A (CW20076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2422. CIRMi15V-A (CW20077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2423. CIRMi15W-A (CW20078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2424. CIRMi15X-A (CW20079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2425. CIRMi15Y-A (CW20080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2426. CIRMi15Z-A (CW20081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2427. CIRMi16A-A (CW20083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2428. CIRMi16B-A (CW20084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2429. CIRMi16C-A (CW20085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2430. CIRMi16D-A (CW20087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2431. CIRMi16E-A (CW20088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2432. CIRMi16F-A (CW20091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2433. CIRMi16G-A (CW20092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2434. CIRMi16H-A (CW20094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2435. CIRMi16I-A (CW20095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2436. CIRMi16J-A (CW20098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2437. CIRMi16K-A (CW20099)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2438. CIRMi16L-A (CW20100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2439. CIRMi16M-A (CW20101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2440. CIRMi16N-A (CW20103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2441. CIRMi16O-A (CW20104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2442. CIRMi16P-A (CW20105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2443. CIRMi16Q-A (CW20106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2444. CIRMi16R-A (CW20107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2445. CIRMi16S-A (CW20108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2446. CIRMi16T-A (CW20109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2447. CIRMi16U-A (CW20110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2448. CIRMi16V-A (CW20111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2449. CIRMi16W-A (CW20112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2450. CIRMi16X-A (CW20115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2451. CIRMi16Y-A (CW20116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2452. CIRMi16Z-A (CW20118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2453. CIRMi17A-A (CW20121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2454. CIRMi17B-A (CW20122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2455. CIRMi17C-A (CW20123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2456. CIRMi17D-A (CW20124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2457. CIRMi17E-A (CW20125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2458. CIRMi17F-A (CW20126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2459. CIRMi17G-A (CW20128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2460. CIRMi17H-A (CW20129)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2461. CIRMi17I-A (CW20131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2462. CIRMi17J-A (CW20132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2463. CIRMi17K-A (CW20133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2464. CIRMi17L-A (CW20135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2465. CIRMi17M-A (CW20136)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2466. CIRMi17N-A (CW20137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2467. CIRMi17O-A (CW20139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2468. CIRMi17P-A (CW20140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2469. CIRMi17Q-A (CW20141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2470. CIRMi17R-A (CW20142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2471. CIRMi17S-A (CW20144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2472. CIRMi17T-A (CW20146)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2473. CIRMi17U-A (CW20149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2474. CIRMi17V-A (CW20150)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2475. CIRMi17W-A (CW20151)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2476. CIRMi17X-A (CW20152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2477. CIRMi17Y-A (CW20153)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2478. CIRMi17Z-A (CW20156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2479. CIRMi18A-A (CW20158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2480. CIRMi18B-A (CW20164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2481. CIRMi18C-A (CW20166)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2482. CIRMi18D-A (CW20167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2483. CIRMi18E-A (CW20170)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2484. CIRMi18F-A (CW20178)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2485. CIRMi18G-A (CW20179)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2486. CIRMi18H-A (CW20181)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2487. CIRMi18I-A (CW20183)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2488. CIRMi18J-A (CW20184)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2489. CIRMi18K-A (CW20185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2490. CIRMi18L-A (CW20186)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2491. CIRMi18M-A (CW20188)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2492. CIRMi18N-A (CW20192)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2493. CIRMi18O-A (CW20193)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2494. CIRMi18P-A (CW20195)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2495. CIRMi18Q-A (CW20196)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2496. CIRMi18R-A (CW20200)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2497. CIRMi18S-A (CW20201)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2498. CIRMi18T-A (CW20202)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2499. CIRMi18U-A (CW20203)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2500. CIRMi18V-A (CW20204)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2501. CIRMi18W-A (CW20206)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2502. CIRMi18X-A (CW20207)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2503. CIRMi18Y-A (CW20209)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2504. CIRMi18Z-A (CW20210)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2505. CIRMi19A-A (CW20212)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2506. CIRMi19B-A (CW20213)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2507. CIRMi19C-A (CW20214)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2508. CIRMi19D-A (CW20222)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2509. CIRMi19E-A (CW20225)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2510. CIRMi19F-A (CW20226)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2511. CIRMi19G-A (CW20231)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2512. CIRMi19H-A (CW20235)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2513. CIRMi19I-A (CW20237)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2514. CIRMi19J-A (CW20239)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2515. CIRMi19K-A (CW20240)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2516. CIRMi19L-A (CW20242)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2517. CIRMi19M-A (CW20243)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2518. CIRMi19N-A (CW20245)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2519. CIRMi19O-A (CW20249)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2520. CIRMi19P-A (CW20252)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2521. CIRMi19Q-A (CW20273)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2522. CIRMi19R-A (CW20277)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2523. CIRMi19S-A (CW20278)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2524. CIRMi19T-A (CW20284)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2525. CIRMi19U-A (CW20295)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2526. CIRMi19V-A (CW20296)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2527. CIRMi19W-A (CW20299)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2528. CIRMi19X-A (CW20300)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2529. CIRMi19Y-A (CW20303)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2530. CIRMi19Z-A (CW20311)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2531. CIRMi20A-A (CW20320)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2532. CIRMi20B-A (CW20321)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2533. CIRMi20C-A (CW20322)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2534. CIRMi20D-A (CW20323)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2535. CIRMi20E-A (CW20324)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2536. CIRMi20F-A (CW20325)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2537. CIRMi20G-A (CW20326)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2538. CIRMi20H-A (CW60040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2539. CIRMi20I-A (CW60109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2540. CMCi001-A (CMC-KIN-hiPSC)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Karyomegalic interstitial nephritis

  2541. UCSFi001-A-78 (WTC11-KL-GFP)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Healthy

  2542. UCSFi001-A-82 (WTC11-SLC12A3)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Gitelman syndrome

  2543. CMCi002-A (CMC-GIT-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Gitelman syndrome

  2544. CMCi006-A (CMC-Fb-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

  2545. CMCi006-A-1 (CMC-Fb001(A4GALT-KO))

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

  2546. CMCi007-A (CMC-Fb-004)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

  2547. CMCi009-A (CMC-BHD-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Birt-hogg-dube syndrome

  2548. CMCi010-A (CMC-Fb-002)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

  2549. CMCi011-A (CMC-DENT-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Dent disease

  2550. CMDi001-A (01016)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  2551. CMDi002-A (01173)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  2552. CMDi003-A (01174)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  2553. CMDi004-A (01175)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  2554. CMDi005-A (01176)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  2555. CMGANTi003-A (SEMD1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  2556. CMGANTi004-A (SEMD2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  2557. CMGANTi005-A (iPSC_MFS_FBN1_MCE-KB_C8)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Marfan syndrome

  2558. CMGANTi006-A (SEDC1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Spondyloepiphyseal dysplasia congenita

  2559. CMGANTi007-A (SEDC2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Spondyloepiphyseal dysplasia congenita

  2560. CMGANTi008-A (iPSC_MFS_FBN1_Fi930129_C8)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Marfan syndrome

  2561. CMUi002-A

    China Capital Medical University (CMU)
    Disease:

    Normal (average)

  2562. CMUi002-A-1 (NONO-KO-iPSCs)

    China Capital Medical University (CMU)
    Disease:

    Left ventricular noncompaction cardiomyopathy

    Disease:

    Intellectual developmental disorder

  2563. CPGHi004-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal (average)

  2564. CPGHi006-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Autosomal dominant polycystic kidney disease

  2565. CPGHi007-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal (average)

  2566. CPGHi008-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Autosomal recessive polycystic kidney disease

  2567. CRICKi001-A (iFCI001)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Intellectual disability

  2568. CRICKi002-A (iFCI027)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Intellectual disability

  2569. CRICKi003-A (iFCI002)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Intellectual disability

  2570. CRICKi004-A (iFCI008)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Spinal muscular atrophy with lower extremity predominant

  2571. CRICKi005-A (iFCI004)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_spinal muscular atrophy

  2572. CRICKi006-A (iFCI005)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_spinal muscular atrophy

  2573. CRICKi007-A (iFCI009)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Spinal muscular atrophy with lower extremity predominant

  2574. CRICKi008-A (iFCI006 and NH13-0078)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    X-linked centronuclear myopathy

  2575. CRICKi009-A (iFCI012 and iFCI012 CLONE 4)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Vhl

  2576. CRICKi010-A (iFCI013 and iFCI013 Clone 7)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Vhl

  2577. CRICKi011-A (iFCI016)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Young-onset parkinson disease

  2578. CRICKi012-A (iFCI017)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Young-onset parkinson disease

  2579. CRICKi013-A (iFCI018 Clone 6)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Von hippel-lindau disease tumor suppressor

  2580. CRICKi014-A (iFCI019 Clone 4)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Von hippel-lindau disease tumor suppressor

  2581. CRICKi015-A (iFCI020 Clone 1)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Von hippel-lindau disease tumor suppressor

  2582. CRICKi016-A (iFCI021 Clone 7)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung cancer

  2583. CRICKi017-A (iFCI022 Clone 4)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung cancer

  2584. CRICKi018-A (iKER 12 and iFCI023)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  2585. CRICKi019-A (iKER 8 and iFCI024)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  2586. CRICKi020-A (iFCI025 and iKER 10)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  2587. CRICKi021-A (iFCI007)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Ullrich congenital muscular dystrophy

  2588. CRICKi022-A (iFCI031)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung cancer

  2589. CRICKi023-A (iFCI032)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung squamous cell carcinoma

  2590. CRICKi024-A (XXY-A4)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2591. CRICKi024-B (XXY-2A1)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2592. CRICKi024-C (XXY-3A9)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2593. CRICKi024-D (2A6 C08)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2594. CRICKi024-E (2A6 C11)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2595. CRICKi024-F (2A6 E11)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2596. CRICKi024-G (2A6 H06)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2597. CRICKi024-G-1 (2A6 H06_XO)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2598. CRICKi024-H (3A21)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2599. CRICKi024-H-1 (3A21_XO)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2600. CRICKi024-I (3A43)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2601. CRICKi024-I-1 (3A43_XO)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Obsolete_klinefelter's syndrome

  2602. CRICKi025-A (iFCI033 CL7)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  2603. CRICKi026-A (iFCI035 CL1)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  2604. CRICKi030-A (FCI042_cl3)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Developmental delay

  2605. CRICKi030-B (FCI042_cl6)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Developmental delay

  2606. CRICKi031-A (FCI043 cl3 and WIPI2-1)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Neurodevelopmental disorder

  2607. CRICKi031-B (FCI043 cl7 and WIPI2-2)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Neurodevelopmental disorder

  2608. CRICKi032-A (FCI044 cl1 and WIPI2-Cntr-1)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  2609. CRICKi032-B (FCI044 cl5 and WIPI2-Cntr-2)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  2610. CRMi001-A (NCRM-5 and NL-5)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal (average)

  2611. CRMi003-A (NCRM-1 and NL-1)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal (average)

  2612. CRMi004-A (CR0000007, NCRM-2 and ND50030)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal (average)

  2613. CRMi005-A (CR0000011, ND50021 and ND1.4)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal (average)

  2614. CRTDi001-A (T12.9 and C1-1)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2615. CRTDi003-A (CRTD2)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2616. CRTDi003-B (CRTD3)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2617. CRTDi004-A (CRTD1)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2618. CRTDi005-A (CRTD4)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2619. CRTDi005-B (CRTD5)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2620. CRTDi006-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  2621. CRTDi006-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  2622. CRTDi007-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  2623. CRTDi007-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  2624. CRTDi008-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  2625. CRTDi009-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  2626. CRTDi010-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  2627. CRTDi011-A (IDP52555 #9)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2628. CRTDi011-B (IDP52555 #13)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2629. CRTDi011-C (IDP52555 #36)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2630. CRTDi011-D (IDP52555 #44)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2631. CSBZZUi001-A (CSBZZU_PS1_001)

    China The first affiliated Hospital of Zhengzhou University (CSBZZU)
    Disease:

    Alzheimer disease

  2632. CSBZZUi002-A

    China The first affiliated Hospital of Zhengzhou University (CSBZZU)
    Disease:

    Normal (average)

  2633. CSBZZUi003-A

    China The first affiliated Hospital of Zhengzhou University (CSBZZU)
    Disease:

    Normal (average)

  2634. CSBZZUi004-A

    China The first affiliated Hospital of Zhengzhou University (CSBZZU)
    Disease:

    Normal (average)

  2635. CSCIi001-A (niPSC HDF16 and niPSC-16.2b)

    United Kingdom Wellcome Trust - MRC Stem Cell Institute (CSCI)
    Disease:

    Normal (average)

  2636. CSCIi002-A (niPSC HDF75 and niPSC-75.1c2)

    United Kingdom Wellcome Trust - MRC Stem Cell Institute (CSCI)
    Disease:

    Normal (average)

  2637. CSIRi001-A (CSIR-SA-001-J4)

    South Africa Council for Scientific and Industrial Research South Africa (CSIR)
    Disease:

    Normal (average)

  2638. CSIRi001-B (CSIR-SA-001-J3)

    South Africa Council for Scientific and Industrial Research South Africa (CSIR)
    Disease:

    Normal (average)

  2639. CSIRi002-A (CSIR-SA-001-L2)

    South Africa Council for Scientific and Industrial Research South Africa (CSIR)
    Disease:

    Normal (average)

  2640. CSIRi002-B (CSIR-SA-001-L10)

    South Africa Council for Scientific and Industrial Research South Africa (CSIR)
    Disease:

    Normal (average)

  2641. CSMCi001-A (CS011iMEN1-n4)

    United States Cedars Sinai Medical Center, (CSMC)
    Disease:

    Multiple endocrine neoplasia type 1

  2642. CSMCi001-A-1 (CS011iMEN1-n4.Homo5 and CS011MEN1-n4.HomoMut5)

    United States Cedars Sinai Medical Center, (CSMC)
    Disease:

    Multiple endocrine neoplasia type 1

  2643. CSMCi001-A-2 (2. CS011MEN1-n4.Corrected1)

    United States Cedars Sinai Medical Center, (CSMC)
    Disease:

    Multiple endocrine neoplasia type 1

  2644. CSSi001-A (Joub03cl2 and COR419)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Isolated joubert syndrome

  2645. CSSi002-A (HD8yrs)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Juvenile huntington disease

  2646. CSSi003-A (COL04 clE2)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Smith-magenis syndrome

  2647. CSSi004-A (HD256.05 cl1)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Huntington disease

  2648. CSSi005-A (COL03 cl.C3)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Normal (average)

  2649. CSSi006-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Huntington disease

  2650. CSSi007-A (Joub07 cl1 and COR11-NG708)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Isolated joubert syndrome

  2651. CSSi008-A (AT214-01-02)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Dentatorubral pallidoluysian atrophy

  2652. CSSi009-A (GDB1307_Z2#1)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Gnb5-related intellectual disability-cardiac arrhythmia syndrome

  2653. CSSi011-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Amyotrophic lateral sclerosis

  2654. CSSi012-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Amyotrophic lateral sclerosis

  2655. CSSi013-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Normal (average)

  2656. CSSi014-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Mucopolysaccharidosis ii

  2657. CSSi015-A (FC17)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Normal (average)

  2658. CSSi016-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Charcot-marie-tooth disease type 4b3

  2659. CSSi017-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Amyotrophic lateral sclerosis

  2660. CSSi018-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    4h leukodystrophy

  2661. CSSi019-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Normal (average)

  2662. CSSi020-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Smith-magenis syndrome

  2663. CSSi021-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Smith-magenis syndrome

  2664. CSSi022-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Charcot-marie-tooth disease type 2a2b

  2665. CSSi023-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Autosomal dominant optic atrophy

  2666. CSSi024-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Focal cortical dysplasia type iib

  2667. CSUi009-A

    China Central South University (CSU)
    Disease:

    Thrombocytopenia

  2668. CSUASOi013-A

    China Aier School of Ophthalmology (CSUASO)
    Disease:

    Retinitis pigmentosa

  2669. CSUASOi014-A

    China Aier School of Ophthalmology (CSUASO)
    Disease:

    Retinitis pigmentosa

  2670. CSUASOi015-A

    China Aier School of Ophthalmology (CSUASO)
    Disease:

    Retinitis pigmentosa

  2671. CSUXHi001-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Spinocerebellar ataxia type 3

  2672. CSUXHi002-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Spinocerebellar ataxia type 1

  2673. CSUXHi003-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Waardenburg syndrome type 2

  2674. CSUXHi004-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Waardenburg syndrome type 1

  2675. CSUXHi005-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Spinocerebellar ataxia type 3

  2676. CSUXHEi001-A

    China Central South University (CSUXHE)
    Disease:

    Normal (average)

  2677. CSUXHEi002-A

    China Central South University (CSUXHE)
    Disease:

    Normal (average)

  2678. CTEFi001-A (CTEF-hiPSC10 and FNUSA-hiPSC10)

    Czech Republic Cell and Tissue Engineering Facility (CTEF)
    Disease:

    Normal (average)

  2679. CTGUi001-A (FD01 and F01)

    China China Three Gorges University (CTGU)
    Disease:

    Fabry disease

  2680. CTGUi002-A

    China China Three Gorges University (CTGU)
    Disease:

    Perrault syndrome 5

  2681. CTUi001-A

    China GIBH (CTU)
    Disease:

    Normal (average)

  2682. CTUi005-A (RD001)

    China GIBH (CTU)
    Disease:

    Neurodevelopmental disorder

  2683. CTUi006-A

    China GIBH (CTU)
    Disease:

    Normal (average)

  2684. CUBi001-A

    Germany Charité - Universitätsmedizin Berlin (CUB)
    Disease:

    Mirage syndrome

  2685. CUBi002-B

    Germany Charité - Universitätsmedizin Berlin (CUB)
    Disease:

    Mirage syndrome

  2686. CUIMCi001-A (ND50003 and FA0000010)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Normal (average)

  2687. CUIMCi002-A (ND50004 and FA0000011)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Normal (average)

  2688. CUIMCi004-A (1514_1)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Class 3 obesity

  2689. CUIMCi004-A-1 (1514_1 #1 CL25)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Class 3 obesity

  2690. CUIMCi004-A-2 (1514_1 #1 CL3)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Class 3 obesity

  2691. CUIMCi004-B

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Class 3 obesity

  2692. CUIMCi005-A (BB#2 and BB9068#2)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Stargardt disease

  2693. CVTTHi001-A

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)
    Disease:

    Activated pi3k-delta syndrome

  2694. CVTTHi001-A-1

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)
    Disease:

    Activated pi3k-delta syndrome

  2695. CVTTHi002-A

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)

  2696. CVTTHi003-A

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)

  2697. CVTTHi004-A

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)

  2698. DANi001-C (iPS-CCD-C3)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Normal (average)

  2699. DANi002-C (GBA-002-C3)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2700. DANi003-H (GBA-003-C8)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2701. DANi004-A (PRKN-004-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2702. DANi005-A (LRRK2-GBA-005-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2703. DANi006-F (GBA-006-C6)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2704. DANi007-A (PINK1-007-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2705. DANi008-F (SNCA-008-C6)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2706. DANi009-C (SNCA-009-C3)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2707. DANi010-A (GBA-010-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2708. DANi011-A (LRRK2-011-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2709. DHMi001-A (Control_S)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2710. DHMi002-A (HLHS_606)

    Germany German Heart Center Munich (DHM)
    Disease:

    Hypoplastic left heart syndrome

  2711. DHMi003-A (HLHS_612)

    Germany German Heart Center Munich (DHM)
    Disease:

    Hypoplastic left heart syndrome

  2712. DHMi004-A (HOS_1460)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2713. DHMi004-A-1 (HOS_1460corr 127 Clone 31)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2714. DHMi004-A-2 (HOS_1460_FLAG Clone 4)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2715. DHMi004-A-3 (HOS_1460corr 127 Clone 31_FLAG Clone 18)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2716. DHMi004-A-4 (1460corr_IDT Cl.127_FlagT Clone 7)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2717. DHMi004-A-5 (1460corr_IDT Cl.127_FlagT Clone 25)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2718. DHMi004-A-6 (1460corr_IDT Cl.127_FlagT Clone 26)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2719. DHMi005-A (Control_L)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2720. DHMi005-A-1 (L_mut)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2721. DHMi005-A-2 (L_FLAG Clone 5)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2722. DHMi005-A-3 (L_FLAG Clone 6)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2723. DHMi005-A-4 (L_FLAG Clone 7)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2724. DHMi005-A-5 (L_mut_FLAG Clone 4)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2725. DHMi005-A-6 (L_mut_FLAG Clone 14)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2726. DHMi005-A-7 (L_mut_FLAG Clone 15)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2727. DHMi005-A-8 (L Delta B2M Clone 6)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2728. DHMi005-A-9 (L Delta B2M Clone 11)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2729. DHMCi010-A (Neph021C)

    Germany Dietmar Hopp Metabolic Center (DHMC)
    Disease:

    Congenital nephrotic syndrome, finnish type

  2730. DHMCi019-A (Neph018C)

    Germany Dietmar Hopp Metabolic Center (DHMC)
    Disease:

    Familial nephrotic syndrome

  2731. DKFZi001-A (clone 30)

    Germany German Cancer Research Center (DKFZ)
    Disease:

    6q27

    Disease:

    Medulloblastoma

  2732. DKFZi001-B (clone 102)

    Germany German Cancer Research Center (DKFZ)
    Disease:

    6q27

    Disease:

    Medulloblastoma

  2733. DMBi001-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Normal (average)

  2734. DMBi001-A-1

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Laminin alpha 2-related dystrophy

  2735. DMBi001-A-2

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Normal (average)

  2736. DMBi003-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Rheumatoid arthritis

  2737. DMBi004-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Rheumatoid arthritis

  2738. DMBi007-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Psoriasis

  2739. DMBi008-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Psoriasis

  2740. DMBi009-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Becker muscular dystrophy

  2741. DMBi009-A-1

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Becker muscular dystrophy

  2742. DMBi010-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Lymphedema-distichiasis syndrome

  2743. DMSCi001-A

    Thailand Department of Medical Sciences (DMSC)
    Disease:

    Normal (average)

  2744. DMSCi002-A

    Thailand Department of Medical Sciences (DMSC)
    Disease:

    Normal (average)

  2745. DPEDi001-A (T12)

    Germany Division of Paediatric Endocrinology and Diabetes (DPED)
    Disease:

    Normal (average)

  2746. DPNJMUi001-A

    China Children's Hospital of Nanjing Medical University (DPNJMU)
    Disease:

    Combined oxidative phosphorylation deficiency 23

  2747. DPNJMUi002-A

    China Children's Hospital of Nanjing Medical University (DPNJMU)
    Disease:

    Progressive familial intrahepatic cholestasis type 3

  2748. DRICUi002-A (ADANG10242CA)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2749. DRICUi003-A (LC56A10005A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2750. DRICUi004-A (LC56A10012A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2751. DRICUi006-A (ADANG10496CA)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2752. DRICUi007-A (ADANG10605CA)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2753. DRICUi010-A (BS38A10004A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2754. DRICUi011-A (BS38A10002A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2755. DRICUi012-A (NT18A10014A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2756. DRICUi013-A (SC45A10021A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2757. DRICUi014-A (CF00C90323A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2758. DRICUi016-A (GU66A10008a)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2759. DRICUi017-A (FB12A10007a)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2760. DRICUi018-A (BH09A10003A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2761. DRICUi019-A (NE37A10024a)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2762. DRICUi020-A (CF00C90474a)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2763. DRICUi022-A (CF00C90161A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2764. DRICUi023-A (NF35A00021A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2765. DRICUi025-A (CF00C90472A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2766. DRICUi026-A (ADCAR24745UC)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2767. DRICUi027-A (ADCAR20186CA)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2768. DRICUi028-A (NE37A10025A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2769. DRICUi029-A (MW14A10014A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2770. DRICUi030-A (CF00C90028A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2771. DVSi001-A (KRAS-Q70L-iPSC)

    China Department of Vascular Surgery, The Second Affiliated Hospital of Soochow University (DVS)
    Disease:

    Varicose veins

  2772. EDi001-A (AST22, AST23 and SAMEA3319992)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2773. EDi001-A-1 (AST22-C and AST23-C)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2774. EDi001-A-2 (AST23-1KO-3, AST22-1KO-3, AST-23_SCAKO Clone 3 and AST-22_SNCAKO Clone 3)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2775. EDi001-A-3 (AST23_SNCAKO Clone 1, AST22-1KO-1, AST23-1KO-1 and AST22_SNCAKO Clone 1)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2776. EDi001-A-4 (AST22-2KO-6, AST23_SNCAKO Clone 6, AST22_SNCAKO Clone 6 and AST23-2KO-6)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2777. EDi001-A-5 (AST23-2KO-II8B)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2778. EDi001-B (AST18)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2779. EDi001-B-1 (AST18-7A)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2780. EDi001-B-2 (AST18-7B)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2781. EDi001-B-3 (AST18-5D)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2782. EDi001-B-4 (AST18-6A)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2783. EDi002-A (NAS2)

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2784. EDi008-B (G51D-4, EDINi008-B, EDIi008-B and SAMEA3174606)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2785. EDi010-A (RCi136)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2786. EDi010-B (RCi138)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2787. EDi011-A (RCi139)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2788. EDi011-B (RCi140)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2789. EDi011-C (RCi141)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2790. EDi012-A (RCi163)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2791. EDi012-B (RCi164)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2792. EDi012-C (RCi165)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2793. EDi013-A (RCi192)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2794. EDi013-B (RCi193)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2795. EDi013-C (RCi214)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2796. EDi014-A (RCi175)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Obsolete_unipolar depression

    Disease:

    Anti-social behavior

  2797. EDi014-B (RCi185)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Obsolete_unipolar depression

    Disease:

    Anti-social behavior

  2798. EDi015-A (RCi176)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Obsolete_unipolar depression

  2799. EDi015-B (RCi183)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Obsolete_unipolar depression

  2800. EDi015-C (RCi184)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Obsolete_unipolar depression

  2801. EDi016-A (RCi189)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2802. EDi016-C (RCi191)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2803. EDi017-A (RCi174)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2804. EDi017-B (RCi181)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2805. EDi017-C (RCi182)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2806. EDi018-A (RCi211)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2807. EDi018-B (RCi212)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2808. EDi018-C (RCi213)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2809. EDi019-A (RCi166)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2810. EDi019-B (RCi167)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2811. EDi019-C (RCi168)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2812. EDi020-A (SFCi55)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2813. EDi021-A (CS0395iCTR-LBCn3)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2814. EDi022-A (CS0617iCTR-LBCn1)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2815. EDi023-A (CS0791iCTR-LBCn1)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2816. EDi024-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2817. EDi025-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2818. EDi026-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2819. EDi027-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2820. EDi028-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2821. EDi029-A

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2822. EDi030-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2823. EDi031-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2824. EDi032-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2825. EDi033-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2826. EDi034-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2827. EDi035-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2828. EDi036-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2829. EDi037-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2830. EDi038-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2831. EDi039-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2832. EDi040-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2833. EDi041-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2834. EDi042-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2835. EDi043-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2836. EDi044-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2837. EDi045-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2838. EDi046-A

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2839. EDIi009-A

    China EdiGene. Inc (EDI)
    Disease:

    Duchenne muscular dystrophy

  2840. EHTJUi002-A (DF-GMP-ZB11AR-H)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2841. EHTJUi003-A (DF-GMP-ZB12AD-H)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2842. EHTJUi004-A (DF-GMP-ZB12AN-I)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2843. EHTJUi005-A (DFGMP-ZB11AL-D)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2844. EHTJUi005-A-1 (ZB11ALD-S16-5)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Werner syndrome

  2845. EHTJUi005-A-3 (ZB11ALD-L4)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Hutchinson-gilford progeria syndrome

  2846. EHTJUi006-A (DFGMP-ZB11AN-B)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2847. EHTJUi007-A (DFGMP-ZB11AO-F)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2848. EMCi169-A (Clone 1)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  2849. EMCi169-B (Clone_3)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  2850. EMCi169-C (Clone_9)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  2851. EMCi169-D (Clone_4)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  2852. EMCi169-E (Clone_11)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  2853. EMCi225-A (Clone_2)

    Netherlands Erasmus MC (EMC)
    Disease:

    Obsolete_neurodevelopmental disorder

  2854. EMCi225-B (Clone_5)

    Netherlands Erasmus MC (EMC)
    Disease:

    Obsolete_neurodevelopmental disorder

  2855. EMCi225-C (Clone_6)

    Netherlands Erasmus MC (EMC)
    Disease:

    Obsolete_neurodevelopmental disorder

  2856. EMCi225-D (Clone_8)

    Netherlands Erasmus MC (EMC)
    Disease:

    Obsolete_neurodevelopmental disorder

  2857. EMCi229-A

    Netherlands Erasmus MC (EMC)
    Disease:

    Normal (average)

  2858. EPFLi001-A (hiPS43)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2859. EPFLi002-A (hiPS9)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2860. EPFLi003-A (hiPS6)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2861. EPFLi004-A (hiPS2)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2862. EPFLi005-A (hiPS45)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2863. EPFLi006-A (hiPS14)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2864. ERPLi004-A (A1AT iPSC C1)

    India Eyestem Research Private Limited (ERPL)
    Disease:

    Alpha 1-antitrypsin deficiency

  2865. ESi001-A (SPO2#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  2866. ESi002-A (SP08#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  2867. ESi003-A ([CRTRd]FiPS3819-4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    X-linked creatine transporter deficiency

  2868. ESi004-A ([GD]FiPS-4F-21c)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Gaucher disease

  2869. ESi005-A (cFA404-KiPS4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Fanconi anemia

  2870. ESi005-B (cFA404-KiPS4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Fanconi anemia

  2871. ESi006-A (SP13#4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  2872. ESi007-A (CBiPS1sv-4F-40)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2873. ESi008-A (KiPS4F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2874. ESi008-B (KiPS3F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2875. ESi028-A (KiPS4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2876. ESi030-A (GA-FiPS4F)

    Spain Spanish Stem Cell Bank (ES)

  2877. ESi031-A (XFiPS-F44-3F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2878. ESi031-B (FiPS-3F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2879. ESi031-C (FiPS-4F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2880. ESi031-D (FiPS-4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2881. ESi032-A (XFiPS-F44-3F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2882. ESi033-A (CBiPS6-2F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2883. ESi034-A (CBiPS30-4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2884. ESi034-B (CBiPS30-4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2885. ESi035-A (AD]FiPSAG07645-4F-17)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_alzheimer's disease

  2886. ESi036-A ([CRTRd]FiPS3067-4F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cerebral creatine deficiency syndrome 1

  2887. ESi037-A (HKiPS-4F)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2888. ESi038-A (CBiPS32-2F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2889. ESi038-B (CBiPS32-3F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2890. ESi038-C (CBiPS32-3F-12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2891. ESi040-A ([PD] FiPS006-4F-11)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_parkinson's disease

  2892. ESi041-A (CBiPS 2F-1c)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2893. ESi041-B (CBiPS 4F-3a)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2894. ESi041-C (CBiPS 4F 10b)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2895. ESi042-A ([TSD] FiPS-4F-3-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Tay-sachs disease

  2896. ESi043-A ([ctrl.PD] FiPS005-4F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2897. ESi044-A (FiPS Ctrl1-mR5F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2898. ESi044-B (FiPS Ctrl1-Ep6F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2899. ESi044-C (FiPS Ctrl1-SV4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2900. ESi044-D (FiPS Ctrl1-R4F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2901. ESi045-A (FiPS Ctrl2-mR5F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2902. ESi045-B (FiPS Ctrl2-Ep6F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2903. ESi045-C (FiPS Ctrl2-SV4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2904. ESi045-D (FiPS Ctrl2-R4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2905. ESi046-A ([UCiPS] Ctrl5-R4F-25)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2906. ESi048-A (MS FiPS 1-R4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

  2907. ESi049-A (MS FiPS 2 R4F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

  2908. ESi050-A (MS FiPS 3-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

  2909. ESi051-A (MS FiPS 4-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

  2910. ESi052-A (MS FiPS 5-R4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

  2911. ESi053-A (MS FiPS 6-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

  2912. ESi054-A (AS FiPS 1-Ep6F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Alport syndrome

  2913. ESi055-A (AS FiPS 2-Ep6F-28)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Alport syndrome

  2914. ESi056-A (AS FiPS 3-Ep6F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Alport syndrome

  2915. ESi057-A ([DUP7] FiPS-4F-3-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2916. ESi057-B ([DUPSW] FiPS301-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2917. ESi058-A ([DUP7] FiPS-4F-4-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2918. ESi058-B ([DUP7] FiPS4-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2919. ESi059-A ([SWB] FiPS-4F-1-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  2920. ESi059-B ([SWB] FiPS1-R4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  2921. ESi060-A ([SWB] FiPS-4F-5-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  2922. ESi060-B ([SWB] FiPS5-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  2923. ESi065-A ([IDDM1] FiPS 1.13-Ep6F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_type i diabetes mellitus

  2924. ESi068-A (SWB FiPS 159-R4F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams-beuren syndrome

  2925. ESi069-A (SWB FiPS 344-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams-beuren syndrome

  2926. ESi070-A (DUPSW FiPS 501-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2927. ESi071-A (DUPSW FiPS 701-R4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2928. ESi072-A (OCD FiPS 1-EP6F-16)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_obsessive-compulsive disorder

  2929. ESi073-A (OCD FiPS 2-EP6F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_obsessive-compulsive disorder

  2930. ESi074-A (CT PBiPS1-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiotoxicity

  2931. ESi075-A (BST PBiPS1-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2932. ESi076-A (BST PBiPS2-Sv4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2933. ESi077-A (CABi001-A and PRPF31-MiPS4F3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Retinitis pigmentosa

  2934. ESi078-A (cPRPF31-MiPS4F7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2935. ESi079-A (cAMDdh09-MiPS4F17)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2936. ESi080-A (N1-FiPS4F#7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2937. ESi081-A (SP11#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2938. ESi082-A (CRB1-MiPS4F1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Macular degeneration

  2939. ESi085-A (cAMDdh01-MiPS4F8 and DH01 c8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2940. ESi086-A (CBiPS8-3F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2941. ESi087-A (BT1-UCiPS4F1 and BT-iPSCs 1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Low grade glioma

  2942. ESi088-A (BT2-UCiPS4F1 and BT-iPSCs 2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Brain cancer

  2943. ESi089-A (Ctrl1-UCiPS4F1 and nonT-iPSCs 1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Inguinal hernia

  2944. ESi090-A (Ctrl2-UCiPS4F1 and nonT-iPSCs 2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cryptorchidism

  2945. ESi091-A (HLA91-MiPS4F3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2946. ESi092-A (HLA98-MiPS4F15)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2947. ESi093-A (CD34 iPS1-Sv4F-B8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2948. ESi094-A (Hz 1-8-3 CBiPS4 Sv4F F6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2949. ESi095-A (Hz 3-7-15 CBiPS3- Sv4F E9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2950. ESi096-A (Hz 11-27-1 CBiPS8-Sv4F-J1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2951. ESi097-A (Hz 24-7-15 CBiPS7 Sv4F-I12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2952. ESi098-A (Hz 30-18-3 CBiPS2-Sv4F-D10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2953. ESi099-A (Hz 33-14-1 CBiPS6-Sv4F H6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2954. ESi100-A (NW FiPS 10II.3-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  2955. ESi101-A (THD FiPS A1 Ep6F-17)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Tyrosine hydroxylase deficiency

  2956. ESi102-A (THD FiPS B1 Ep6F-15)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Tyrosine hydroxylase deficiency

  2957. ESi103-A (OCD FiPS3-Ep6F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_obsessive-compulsive disorder

  2958. ESi104-A (PMM2-CDG FiPS48-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Pmm2-cdg

  2959. ESi106-A (MD FiPS3304-Sv4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Mitochondrial disease

  2960. ESi107-A (TAC PBiPS1-Sv4F-3 and ATTR-CM PBiPS1-Sv4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  2961. ESi108-A (AFib-C53)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Atrial fibrillation

  2962. ESi110-A (HLA89-MiPS4F8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2963. ESi111-A (Ctrl EiPS J9 mR6F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2964. ESi112-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2965. ESi113-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2966. ESi114-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2967. ESi115-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Inclusion body myositis

  2968. ESi116-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Inclusion body myositis

  2969. ESi117-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Inclusion body myositis

  2970. ESi118-A (MD FiPS3236-Sv4F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Mitochondrial disease

  2971. ESi119-A (SPG FiPS1-Ep6F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Hereditary spastic paraplegia

  2972. ESi120-A (RRMS PBiPS11-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  2973. ESi121-A (RRMS PBiPS12-Sv4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  2974. ESi122-A (PPMS PBiPS7-Sv4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  2975. ESi123-A (PPMS PBiPS8-Sv4F-13)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  2976. ESi124-A (PPMS PBiPS9-Sv4F-12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  2977. ESi128-A (PPMS PBiPS10-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  2978. ESi129-A (RRMS PBiPS13-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  2979. ESi130-A (RRMS PBiPS14-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  2980. ESi132-A (PRPF3181-MiPS4F5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Retinitis pigmentosa

  2981. ESi133-A (CT PBiPS2-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Chemically induced cardiotoxicity

  2982. ESi136-A (NDD PBiPS1-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Neurodevelopmental disorders

  2983. ESi137-A (SSP PBiPS P1-Sv4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Spastic paraparesis

  2984. ESi137-B (SSP PBiPSP1-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Spastic paraparesis

  2985. ESi138-A (ATTR CM PBiPS3-Sv4F-14)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  2986. ESi139-A (ATTR CM PBiPS4-Sv4F-13)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  2987. ESi140-A (CT PBiPS3-Sv4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Chemically induced cardiotoxicity

  2988. ESi141-A (BS PBiPS46-Sv4F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Brugada syndrome

  2989. ESi142-A (ATTR CM PBiPS2-Sv4F-16)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  2990. ESi143-A (Ctrl BS PBiPS37-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2991. ESi144-A (SPG FiPS2-Ep6F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Hereditary spastic paraplegia

  2992. ESi145-A (LD FiPS18338-Ep6F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Leukodystrophy

  2993. ESi146-A (NEDCASB FiPS319-Ep6F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities

  2994. ESi147-A (HLD18 FiPS4379-Ep6F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Leukodystrophy, hypomyelinating, 18

  2995. ESi148-A (ALSPBiPS1-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Amyotrophic lateral sclerosis

  2996. ESi149-A (GNB1 FiPS1-Ep6F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Encephalopathy

  2997. ESi150-A (GNB1 FiPS2-Ep6F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Encephalopathy

  2998. ESi151-A (GNB1 FiPS3-Ep6F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Encephalopathy

  2999. ESi152-A (GNB1 FiPS4-Ep6F-12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Encephalopathy

  3000. ESi153-A (ATTR CM PBiPS5-Sv4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  3001. ESi154-A (ATTR CM PBiPS6-Sv4F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  3002. ESi155-A (PMM2 CDG FiPS01-Sv4F-11)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Pmm2-cdg

  3003. ESi156-A (ALD FiPS1-Ep6F-11)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Adrenoleukodystrophy

  3004. ESi157-A (STGD90-MiPS4F10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Stargardt disease

  3005. ESi158-A (STGD73-MiPS4F8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Stargardt disease

  3006. ESi159-A (ALD FiPS2-Ep6F-11)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Adrenoleukodystrophy

  3007. ESi160-A (WFS1 FiPS04-Ep6F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Wolfram syndrome

  3008. ESi160-B (WFS1 FiPS 04-Ep6F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Wolfram syndrome

  3009. ESi162-A (WFS1 FiPS 34-Ep6F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Wolfram syndrome

  3010. ESi162-B (WFS1 FiPS 34-Ep6F-13)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Wolfram syndrome

  3011. ESi164-A (S PBiPS654-Sv4F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Schizophrenia

  3012. ESi165-A (S PBiPS1199-Sv4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Schizophrenia

  3013. ESi167-A (S PBiPS1785-Sv4F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Schizophrenia

  3014. ESi168-A (S PBiPS 1580-Sv4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Schizophrenia

  3015. ESi169-A (S PBiPS1786-Sv4F-12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Schizophrenia

  3016. ESi170-A (S PBiPS1792-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Schizophrenia

  3017. EUSOMi001-A (3-1 and LQTS003-1)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Long qt syndrome 2

  3018. EUSOMi002-A (LQTS003-3-1 and 3-3-1)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Long qt syndrome 2

  3019. EUSOMi003-A (LQTS003-3-2 and 3-3-2)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Normal (average)

  3020. EUSOMi004-A (LQTS007-2-1 and 7-2-1)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Long qt syndrome 1

  3021. EUSOMi005-A (LQTS005-1, 5-1)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Long qt syndrome 1

  3022. EUSOMi006-A (LQTS001-1, 1-1)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Long qt syndrome 1

  3023. EUSOMi007-A (2-1 and LQTS002-1)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Long qt syndrome 1

  3024. EXSURGi001-A (SevXC_MTARC1)

    Germany Charité – Universitätsmedizin Berlin (EXSURG)
    Disease:

    Normal (average)

  3025. FAMRCi001-A (ARVC2)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  3026. FAMRCi001-B (ARVC4)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  3027. FAMRCi002-A (OBC7)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Desminopathy

  3028. FAMRCi003-A (108-1)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Normal (average)

  3029. FAMRCi003-B (108-2)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Normal (average)

  3030. FAMRCi004-A (DSPL1)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Sick sinus syndrome

    Disease:

    Atrioventricular block

    Disease:

    Hereditary progressive cardiac conduction defect

  3031. FAMRCi004-B (DSPL10)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Sick sinus syndrome

    Disease:

    Atrioventricular block

    Disease:

    Hereditary progressive cardiac conduction defect

  3032. FAMRCi005-A (LMNA B4)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Paroxysmal ventricular tachycardia

    Disease:

    Atrioventricular block

    Disease:

    Obsolete_myopathy

  3033. FAMRCi005-B (LMNA B5)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Paroxysmal ventricular tachycardia

    Disease:

    Atrioventricular block

    Disease:

    Obsolete_myopathy

  3034. FAMRCi006-A (LMNA T3)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  3035. FAMRCi006-B (LMNA T4)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  3036. FAMRCi007-A (LMNA #23)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Atrioventricular block

    Disease:

    Paroxysmal atrial fibrillation

  3037. FAMRCi007-B (LMNA #19)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Atrioventricular block

    Disease:

    Paroxysmal atrial fibrillation

  3038. FAMRCi008-A (10X-12)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Normal (average)

  3039. FAMRCi009-A (RCMP43)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Restrictive cardiomyopathy

  3040. FAMRCi010-A (RCMP48)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Restrictive cardiomyopathy

  3041. FAMRCi011-A (ARVC51)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  3042. FAMRCi011-B (ARVC51b)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  3043. FAMRCi012-A (Brug/VT-83)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Ventricular fibrillation

  3044. FAMRCi013-A (ARVC300-14)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  3045. FAMRCi013-B (ARVC300-21)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  3046. FAMRCi013-C (ARVC300-25)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  3047. FAMRCi014-A (177-10)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Hypertrophic cardiomyopathy

  3048. FAMRCi015-A (HCM12f10)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Hypertrophic cardiomyopathy

  3049. FAMRCi015-B (HCM12f23)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Hypertrophic cardiomyopathy

  3050. FAMRCi016-A (RCMP41-2)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Restrictive cardiomyopathy

  3051. FCBRNi001-A

    Russia Federal Center of Brain Research and Neurotechnologies (FCBRN)
    Disease:

    Normal (average)

  3052. FCBRNi002-A

    Russia Federal Center of Brain Research and Neurotechnologies (FCBRN)
    Disease:

    Wilson disease

  3053. FDCHi004-A (iPS-39)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Osteogenesis imperfecta

  3054. FDCHi007-A

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Developmental and epileptic encephalopathy 31a

  3055. FDCHi008-A (JYIPS0087)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Chronic intestinal pseudoobstruction

  3056. FDCHi010-A (iPSCx-y-AHDC1-m)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Xia-gibbs syndrome

  3057. FDCHi011-A (iPSC-XX-700-WDR45-m)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  3058. FDCHi012-A (iPSCx-x-DYRK1A-m)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Dyrk1a-related intellectual disability syndrome

  3059. FDCHi014-A (iPSCx-y-NOVA2-m)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities

  3060. FDCHi015-A

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Hereditary fructose intolerance

  3061. FDCHi016-A (iPSC-XX-888-WDR45-m)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  3062. FDCHDPi001-A (FDCHDP01)

    China Fudan University (FDCHDP)
    Disease:

    Tourette syndrome

  3063. FDHPIi001-A

    China (WITHDRAWN) Fudan University (FDHPI)
    Disease:

    Neurodegeneration

  3064. FDHSi002-A (FDITBRi002-A)

    China Huashan Hospital of Fudan University (FDHS)
    Disease:

    Parkinson disease

  3065. FDHSi003-A

    China Huashan Hospital of Fudan University (FDHS)
    Disease:

    Gordon holmes syndrome

  3066. FDHSi005-A

    China Huashan Hospital of Fudan University (FDHS)
    Disease:

    Gne myopathy

  3067. FDIBSi001-A (iPSCx-x-ADNP-F)

    China Institutes of Brain Science,Fudan University (FDIBS)
    Disease:

    Adnp-related multiple congenital anomalies - intellectual disability - autism spectrum disorder

  3068. FDIBSi002-A (iPSCx-x-DYRK1A-G/A)

    China Institutes of Brain Science,Fudan University (FDIBS)
    Disease:

    Intellectual developmental disorder, autosomal dominant 7

  3069. FDZSi002-A

    China Zhongshan Hospital of Fudan University (FDZS)

  3070. FDZSi003-A

    China Zhongshan Hospital of Fudan University (FDZS)
    Disease:

    Prostate cancer

  3071. FHUSTCi001-A

    China The First Affiliated Hospital of USTC,Division of life Science and Medicine,University of Science and Technology of China (FHUSTC)
    Disease:

    Glomerulopathy

  3072. FHUSTCi002-A

    China The First Affiliated Hospital of USTC,Division of life Science and Medicine,University of Science and Technology of China (FHUSTC)
    Disease:

    Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome

  3073. FINi001-A (FI.SPSM.SCN2A.R1882Q.009)

    Australia The Florey Institute of Neuroscience and Mental Health (FIN)
    Disease:

    Developmental and epileptic encephalopathy

  3074. FINi002-A (FI.CPLT.PRKN.R275W+del_e8.PK006)

    Australia The Florey Institute of Neuroscience and Mental Health (FIN)
    Disease:

    Parkinson disease

  3075. FINi006-A (FI.CS.PRKNDex2/Dex5-7.F@40)

    Australia The Florey Institute of Neuroscience and Mental Health (FIN)
    Disease:

    Parkinson disease

  3076. FINi007-A (FI.SP.SLC6A1/GAT1.G307R.032)

    Australia The Florey Institute of Neuroscience and Mental Health (FIN)

  3077. FINi102-A (FI.SP.KCNT1(R950Q/+).NGF026)

    Australia The Florey Institute of Neuroscience and Mental Health (FIN)
    Disease:

    Epilepsy

  3078. FINCBi001-A (F56Lcl33 and F56L 33M)

    Italy Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
    Disease:

    Leber hereditary optic neuropathy

  3079. FINCBi004-A

    Italy Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
    Disease:

    Neurodegeneration with brain iron accumulation 4

  3080. FINCBi005-A (mt1072 clone #103 and mt1072 #103)

    Italy Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
    Disease:

    Leber hereditary optic neuropathy

  3081. FINCBi006-A (mt1108 clone #121 and mt1108 #121)

    Italy Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
    Disease:

    Leber hereditary optic neuropathy

  3082. FJMAi001-A

    China Fujian Academy of Medical Sciences (FJMA)
    Disease:

    Marfan syndrome

  3083. FJMUi001-A (hiPS-SPG76-001)

    China Fujian Medical University (FJMU)
    Disease:

    Hereditary spastic paraplegia

  3084. FJMUNi001-A

    China Department of Neurology, Fujian Institute of Neurology, the First Affiliated Hospital, Fujian Medical University (FJMUN)
    Disease:

    Duchenne muscular dystrophy

  3085. FJMUUHi001-A

    China Fujian Medical University Union Hospital (FJMUUH)
    Disease:

    Parkinson's disease 7

  3086. FJMUUHi002-A

    China Fujian Medical University Union Hospital (FJMUUH)
    Disease:

    Rett syndrome

  3087. FLENIi004-A (FBAD1)

    Argentina Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia (FLENI)
    Disease:

    Familial alzheimer disease

  3088. FMCPGHi001-A (301-iPSC-normal-001A)

    China The First Medical Center of PLA General Hospital (FMCPGH)
    Disease:

    Normal (average)

  3089. FMCPGHi002-A (301-iPSC-normal-002B)

    China The First Medical Center of PLA General Hospital (FMCPGH)
    Disease:

    Normal (average)

  3090. FMCPGHi003-A (301-iPSC-FHM-001A)

    China The First Medical Center of PLA General Hospital (FMCPGH)
    Disease:

    Familial hemiplegic migraine 3

  3091. FMCPGHi006-A

    China The First Medical Center of PLA General Hospital (FMCPGH)
    Disease:

    Duchenne muscular dystrophy

  3092. FMMUNIi001-A (I-WT)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Normal (average)

  3093. FMMUNIi002-A (I-IF)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Ventricular fibrillation

  3094. FMMUNIi003-A (I-CPVT)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3095. FMUPDCi001-A (ADAT3c.219dupA/c.587C>T)

    China Fetal Medicine unit &Prenatal Diagnosis Center, Shanghai 1st Maternity and Infant Hospital of Tongji University (FMUPDC)
    Disease:

    Intellectual developmental disorder

  3096. FPHYBi001-A (CYY250222)

    China First People’s Hospital of Yibin (FPHYB)
    Disease:

    Normal (average)

  3097. FRIMOi001-A (RP1_FiPS4F1.6)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Retinitis pigmentosa

  3098. FRIMOi002-A (RP2_FiPS4F2.2)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Retinitis pigmentosa

  3099. FRIMOi003-A (STGD1_ FiPS4F1.5)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Stargardt disease

  3100. FRIMOi004-A (STGD2_ FiPS4F1.7)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Stargardt disease

  3101. FRIMOi005-A (RP3_FiPS4F11)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Retinitis pigmentosa

  3102. FRIMOi006-A (BEST1_FiPS4F1)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Bestrophinopathy

  3103. FRIMOi007-A (PDE6C_FiPS4F1)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Achromatopsia

  3104. FSMi001-A (FSM-SPG31-2)

    Italy IRCCS Fondazione Stella Maris (FSM)
    Disease:

    Spastic paraplegia 31

  3105. FUHSi001-A

    China Huashan Hospital of Fudan University (FUHS)
    Disease:

    Obsolete_cervical artery dissection

  3106. GEMi001-A (GN-IPS-12-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3107. GEMi002-A (GN-IPS-14-2)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3108. GEMi003-A (GN-IPS-15-2)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3109. GEMi004-A (GN-IPS-135-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3110. GEMi005-A (GN-IPS-160-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3111. GEMi006-A (GN-IPS-201-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3112. GEMi007-A (GN-IPS-202-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3113. GEMi008-A (GN-IPS-203-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3114. GEMi009-A (GN-IPS-204-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3115. GEMi010-A (GN-IPS-205-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3116. GEMi011-A (GN-IPS-206-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3117. GEMi011-A-1 (GN-JY02-02-011(PSEN1-exon9-KO))

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Alzheimer disease

  3118. GEMi012-A (GN-IPS-207-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3119. GEMi013-A (GN-IPS-208-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3120. GEMi014-A (GN-IPS-209-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3121. GEMi015-A (GN-IPS-210-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3122. GEMi016-A (GN-IPS-211-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3123. GEMi017-A (GN-IPS-212-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3124. GEMi018-A (GN-IPS-213-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3125. GEMi019-A (GN-IPS-214-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3126. GEMi020-A (GN-IPS-215-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3127. GEMi021-A (GN-IPS-216-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3128. GEMi022-A (GN-IPS-217-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3129. GEMi022-A-1 (GN-JY02-01-001(APP c.2010-2011 inv))

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Alzheimer disease

  3130. GEMi022-A-2 (GN-JY02-01-008(PSEN1 c.313T>C))

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Alzheimer disease

  3131. GEMi022-A-3 (GN-JY02-01-012(APP c.2149G>A))

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Alzheimer disease type 1

  3132. GEMi023-A (GN-IPS-218-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3133. GEMi024-A (GN-IPS-219-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3134. GEMi025-A (GN-IPS-220-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3135. GEMi026-A (GN-IPS-46-3)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3136. GENYOi001-A (PBMC1-iPS4F1)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal (average)

  3137. GENYOi003-A (PBMC2-iPS4F8)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal (average)

  3138. GENYOi004-A (ASD-PBMC-iPS4F2)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Helsmoortel-van der aa syndrome

  3139. GENYOi005-A (FPD/AML-PBMC-iPSC4F73)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Familial platelet disorder with associated myeloid malignancy

  3140. GENYOi006-A (GRX-MCiPS4F-A2)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal (average)

  3141. GENYOi006-A-1 (GRX-MCiPS4F-A2-ETO2-GLIS2)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Acute myeloid leukemia

  3142. GENYOi006-A-2 (GRX-MCiPS4F-A2-NEO)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal (average)

  3143. GENYOi007-A (W8)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Obsolete_meniere disease

  3144. GIBHi001-A

    China Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences (GIBH)
    Disease:

    Autism spectrum disorder

  3145. GIBHi002-A (C11)

    China Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences (GIBH)
    Disease:

    Normal (average)

  3146. GIBHi002-A-1 (C5-PARK2-KO)

    China Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences (GIBH)
    Disease:

    Parkinson disease

  3147. GIBHi003-A (PINK1-I368N-C2)

    China Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences (GIBH)
    Disease:

    Parkinson disease

  3148. GLNNFi001-A

    India GROW Laboratory (GLNNF)
    Disease:

    Macular corneal dystrophy

  3149. GRi001-A (572)

    France Gustave Roussy (GR)
    Disease:

    Normal (average)

  3150. GRi002-A (534)

    France Gustave Roussy (GR)
    Disease:

    Normal (average)

  3151. GRi003-A

    France Gustave Roussy (GR)
    Disease:

    Normal (average)

  3152. GRCHJUi001-A (LYJ-iPS-C)

    China Guangzhou Red Cross Hospital of Jinan University (GRCHJU)
    Disease:

    Atrial fibrillation

  3153. GWCMCi001-A (iPS-57)

    China Guangzhou Women and Children's Medical Center (GWCMC)
    Disease:

    Obsolete_iga glomerulonephritis

  3154. GWCMCi005-A (GWCMCi-TANC2)

    China Guangzhou Women and Children's Medical Center (GWCMC)
    Disease:

    Lennox-gastaut syndrome

  3155. GWCMCi006-A (GWCMCi-GRIN1)

    China Guangzhou Women and Children's Medical Center (GWCMC)
    Disease:

    Obsolete_neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant

  3156. GZHMCi011-A (SCA3-LXM)

    China The Third Affiliated Hospital of Guangzhou Medical University (GZHMC)
    Disease:

    Normal (average)

  3157. HCORDi001-A (M2_IPSC3_A)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3158. HCORDi001-B (M2_IPSC3_B)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3159. HCORDi001-C (M2_IPSC3_C)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3160. HCORDi001-D (M2_IPSC3_K)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3161. HCORDi001-E (M2_IPSC3_L)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3162. HCORDi001-F (M2_IPSC3_M)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3163. HCORDi001-G (M2_IPSC3_N)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3164. HCORDi001-H (M2_IPSC3_O)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3165. HCORDi001-I (M2_IPSC4_P)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3166. HCORDi001-J (M2_IPSC4_R)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3167. HDZi001-A (hiPSC NP0039)

    Germany Heart and Diabetes Center North Rhine Westphalia (HDZ)
    Disease:

    Arrhythmogenic right ventricular dysplasia 5

  3168. HDZi003-A (hiPSC NP0038)

    Germany Heart and Diabetes Center North Rhine Westphalia (HDZ)
    Disease:

    Arrhythmogenic right ventricular dysplasia 5

  3169. HDZi003-A-1

    Germany Heart and Diabetes Center North Rhine Westphalia (HDZ)
    Disease:

    Arrhythmogenic right ventricular dysplasia 5

  3170. HEBHMUi001-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Parkinson disease

  3171. HEBHMUi002-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3172. HEBHMUi003-A (HCHB-003)

    China Hebei Medical University (HEBHMU)
    Disease:

    Amyotrophic lateral sclerosis

  3173. HEBHMUi004-A (ALSHB-004)

    China Hebei Medical University (HEBHMU)
    Disease:

    Amyotrophic lateral sclerosis

  3174. HEBHMUi005-A (HCHB-005)

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3175. HEBHMUi007-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3176. HEBHMUi008-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Cerebrovascular disease

  3177. HEBHMUi009-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Obsolete_alzheimer's disease

  3178. HEBHMUi010-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3179. HEBHMUi011-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Obsolete_alzheimer's disease

  3180. HEBHMUi012-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Hypertension

  3181. HEBHMUi013-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Alzheimer's disease

  3182. HEBHMUi014-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Alzheimer disease

  3183. HEBHMUi015-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3184. HEBHMUi017-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3185. HEBHMUi018-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Baraitser-winter syndrome 1

  3186. HELPi001-A (BS-TL-1)

    China Help Stem Cell Innovations Co.Ltd. (HELP)
    Disease:

    Congenital contractural arachnodactyly

  3187. HHUi003-B (A4_C1)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Maternally-inherited leigh syndrome

  3188. HHUi003-C (A4_W1)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Maternally-inherited leigh syndrome

  3189. HHUi006-A (11656_H)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Normal (average)

  3190. HHUi006-B (11656_K)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Normal (average)

  3191. HHUUKDi001-A (ISRM-UM51 and UM51-iPSC)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Normal (average)

  3192. HHUUKDi009-A (TFBJ)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Normal (average)

  3193. HHUUKDi011-A (AATD iPSC-1 and ISRM-AATD-iPSC-1)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Alpha-1 antitrypsin deficiency

  3194. HHUUKDi012-A (AATD iPSC-2 and ISRM-AATD-iPSC-2)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Alpha-1 antitrypsin deficiency

  3195. HHUUKDi013-A (ISRM-AATD-iPSC-3)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Alpha-1 antitrypsin deficiency

  3196. HHUUKDi014-A (ISRM-BS3-iPSC)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)

  3197. HIHCNi008-A (iPSC-CO-4)

    Germany Hertie Institute for Clinical Brain Research - Clinical Neurogenetics (HIHCN)
    Disease:

    Normal (average)

  3198. HIHCNi008-A-3 (iPSC-REEP1_homKO2)

    Germany Hertie Institute for Clinical Brain Research - Clinical Neurogenetics (HIHCN)
    Disease:

    Hereditary spastic paraplegia 31

  3199. HIHCNi008-A-4 (iPSC-REEP1_hetKO2)

    Germany Hertie Institute for Clinical Brain Research - Clinical Neurogenetics (HIHCN)
    Disease:

    Hereditary spastic paraplegia 31

  3200. HIHCNi008-A-5 (iPSC-M1SPAST_homKO2)

    Germany Hertie Institute for Clinical Brain Research - Clinical Neurogenetics (HIHCN)
    Disease:

    Autosomal dominant spastic paraplegia type 4

  3201. HIHCNi008-A-6 (iPSC-M1SPAST_hetKO2)

    Germany Hertie Institute for Clinical Brain Research - Clinical Neurogenetics (HIHCN)
    Disease:

    Autosomal dominant spastic paraplegia type 4

  3202. HIHDNDi001-A (A30P-3, SNCA3 and Tue_020_A)

    Germany Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tuebingen (HIHDND)
    Disease:

    Autosomal dominant parkinson disease 1

  3203. HIHDNDi001-B (A30P-4, SNCA4 and Tue_020_B)

    Germany Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tuebingen (HIHDND)
    Disease:

    Autosomal dominant parkinson disease 1

  3204. HIHRSi004-A

    Germany Hertie Institute for Clinical Brain Research, AG Schüle (HIHRS)
    Disease:

    Spastic ataxia

  3205. HIHRSi005-A

    Germany Hertie Institute for Clinical Brain Research, AG Schüle (HIHRS)
    Disease:

    Spastic ataxia

  3206. HIHRSi006-A

    Germany Hertie Institute for Clinical Brain Research, AG Schüle (HIHRS)
    Disease:

    Spastic ataxia

  3207. HIMRi001-A (p.Q1662X FLNC hiPSCs)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Muscle filaminopathy

  3208. HIMRi002-A (p.A46T CAV3 hiPSCs #1)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Caveolinopathy

  3209. HIMRi003-A (p.A46T CAV3 hiPSCs #2)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Caveolinopathy

  3210. HIMRi004-A (FLNC p.W2710X hiPSC)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Muscle filaminopathy

  3211. HIMRi005-A (FLNC p.Y2704X hiPSC)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Muscle filaminopathy

  3212. HIMRi006-A (GAA c.307T>G hiPSC)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Glycogen storage disease due to acid maltase deficiency, infantile onset

  3213. HIMRi007-A (GAA c.-32-13T>G, c.1716C>G hiPSC)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Glycogen storage disease due to acid maltase deficiency, late-onset

  3214. HKUi002-A (AYC12 and HKUi002-A-AYC12)

    Hong Kong The University of Hong Kong (HKU)
    Disease:

    Dilated cardiomyopathy

  3215. HMGUi001-A (XM001 and BIHi043-A)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Normal (average)

  3216. HMGUi001-A-1 (hINS-T2A-H2B-Cherry (+/-) and HMGUi001-A-1)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Normal (average)

  3217. HMGUi002-A (XM002)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Normal (average)

  3218. HMGUi003-A

    Germany Helmholtz Zentrum München (HMGU)

  3219. HMGUi004-A

    Germany Helmholtz Zentrum München (HMGU)

  3220. HMGUi005-A (150553)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  3221. HMGUi006-A (152350)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  3222. HMSi001-A (GM27938)

    United States Harvard Medical School (HMS)
    Disease:

    Kif1a related neurological disorder

  3223. HMSi001-B (GM27937)

    United States Harvard Medical School (HMS)
    Disease:

    Kif1a related neurological disorder

  3224. HMSi002-A (GM27934)

    United States Harvard Medical School (HMS)
    Disease:

    Kif1a related neurological disorder

  3225. HMSCATi001-A

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Normal (average)

  3226. HMSCATi002-A

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Normal (average)

  3227. HMSCATi003-A (PJW)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Parkinson disease

  3228. HMSCATi004-A (LHK)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Young-onset parkinson disease

  3229. HMSCATi005-A (LQH)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Alzheimer's disease

  3230. HMSCATi006-A (CYJ-C1)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Epileptic encephalopathy

  3231. HMSCATi007-A (GXM)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Epilepsy, familial focal, with variable foci 1

  3232. HMSCATi008-A (TSC1-PL)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Tuberous sclerosis

    Disease:

    Epilepsy

  3233. HMSCATi009-A (WZX)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Frontotemporal dementia

  3234. HMUCPi001-A

    China Harbin Medical University College of Pharmacy (HMUCP)
    Disease:

    Hypertrophic cardiomyopathy

  3235. HNMUi002-A (iPS-UC1291)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  3236. HNMUi003-A (iPS-UC1290)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  3237. HNMUi004-A (iPS-AF717)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  3238. HNMUi005-A (iPS-UC1056)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  3239. HNMUi006-A (iPS-UC1055)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  3240. HNMUi007-A (iPS-AF0442)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  3241. HNMUi008-A (iPS-UC2419)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  3242. HNMUi009-A (iPS-UC1171)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  3243. HNMUi010-A (iPS-AF091)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  3244. HPCHi001-A

    China Henan Provincial Chest Hospital (HPCH)
    Disease:

    Familial hypercholesterolemia

  3245. HPCHi002-A

    China Henan Provincial Chest Hospital (HPCH)
    Disease:

    Dilated cardiomyopathy

  3246. HPIi005-A (RYR1-5-9214-iPSC clone R5)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  3247. HPIi005-B (RYR1-5-9214-iPSC clone R11)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  3248. HPIi006-A (RYR1-3278-R2A)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  3249. HPIi008-A (RYR1-4833-R7)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  3250. HPIi009-A (RYR1-15377-R1B)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  3251. HPIi010-A (MYH7-17773-R4A)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Myh7-related skeletal myopathy

  3252. HPIi011-A (MYH7-18681-R1A)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Myh7-related skeletal myopathy

  3253. HPIi012-A (MYH7-19203-R1D)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Myh7-related skeletal myopathy

  3254. HPIi013-A (OPDM_ABCD3)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Oculopharyngodistal myopathy

  3255. HUBi001-A (HUB001Ai)

    Netherlands The Hubrecht Institute (HUB)
    Disease:

    Normal (average)

  3256. HUJIi001-A (iWSM-F1)

    Israel Hebrew University of Jerusalem (HUJI)
    Disease:

    Developmental and epileptic encephalopathy, 28

  3257. HUJIi002-A (iWSM-M2)

    Israel Hebrew University of Jerusalem (HUJI)
    Disease:

    Developmental and epileptic encephalopathy, 28

  3258. HUJIi003-A (iWSM-S5)

    Israel Hebrew University of Jerusalem (HUJI)
    Disease:

    Developmental and epileptic encephalopathy, 28

  3259. HUJIi004-A (ITM-iPS10)

    Israel Hebrew University of Jerusalem (HUJI)

  3260. HUJIi004-B (ITM-iPS11)

    Israel Hebrew University of Jerusalem (HUJI)

  3261. HUJIi005-A (ID-iPS7)

    Israel Hebrew University of Jerusalem (HUJI)

  3262. HUJIi005-B (ID-iPS10)

    Israel Hebrew University of Jerusalem (HUJI)

  3263. HUSTTJi001-A

    China Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology (HUSTTJ)
    Disease:

    Moyamoya disease

  3264. HVRDi004-B (GM23338)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  3265. HVRDi004-B-1 (ENCBS369AAA and iNGN)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  3266. HVRDi005-A (BJ SiPS-D)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  3267. HVRDi006-A (18b healthy control)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  3268. HVRDi007-A (DiPS 1016SevA)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  3269. HVRDi008-A (SOD1-27e and 27e)

    United States Harvard University (HVRD)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  3270. HVRDi009-A (29e SOD1 L144F and 29e)

    United States Harvard University (HVRD)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  3271. HVRDi010-A (19a)

    United States Harvard University (HVRD)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  3272. HZSMHCi001-A

    China Hangzhou Seventh People’s Hospital Mental Health Center, Zhejiang University School of Medicine (HZSMHC)
    Disease:

    Bipolar disorder

  3273. HZSMHCi002-A

    China Hangzhou Seventh People’s Hospital Mental Health Center, Zhejiang University School of Medicine (HZSMHC)
    Disease:

    Neuronal intranuclear inclusion disease

  3274. HZSMHCi003-A

    China Hangzhou Seventh People’s Hospital Mental Health Center, Zhejiang University School of Medicine (HZSMHC)
    Disease:

    Fragile x syndrome

  3275. HZSMHCi004-A

    China Hangzhou Seventh People’s Hospital Mental Health Center, Zhejiang University School of Medicine (HZSMHC)
    Disease:

    Major depressive disorder

  3276. IAIi001-A (IAIi001RSTS2-65-A)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  3277. IAIi002-A (IAIi002RSTS1-34-A)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  3278. IAIi003-A (IAIi003RSTS1-46-A)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  3279. IAIi004-A (IAIi004RSTS1-149-A)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  3280. IAIi005-A (AC52)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Normal (average)

  3281. IAIi006-A (BC6)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Amyotrophic lateral sclerosis

  3282. IAIi007-A (CC5)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Amyotrophic lateral sclerosis

  3283. IAIi008-A (DC2)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Amyotrophic lateral sclerosis

  3284. IAIi009-A (EC1)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Normal (average)

  3285. IAIi010-A (Kif5A 1847 C3)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Autosomal dominant spastic paraplegia type 10

  3286. IBBISTi004-A (AS-GB clone 12)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  3287. IBBISTi004-B (AS-GB clone 20)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  3288. IBBISTi004-C (AS-GB clone 22)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  3289. IBBISTi005-A (F81 (940) clone 5)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3290. IBBISTi005-B (F81 (940) clone 8)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3291. IBBISTi006-A (F93 clone 5)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3292. IBBISTi006-B (F93 clone 6)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3293. IBBISTi007-A (6F26)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3294. IBBISTi007-B (2F26)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3295. IBBISTi008-A (8F82)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3296. IBBISTi008-B (3F82)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3297. IBBISTi009-A (1F97)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3298. IBBISTi009-B (5F97)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3299. IBBISTi010-A (4_H17)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3300. IBBISTi011-A (3_H24)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3301. IBBISTi012-A (6_H35)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3302. IBBISTi013-A (4_H22)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3303. IBBISTi014-A (Ctrl-MD1 (clone O))

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Normal (average)

  3304. IBBISTi015-A (AS-MD1 (clone N))

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  3305. IBBISTi016-A (Ctrl-MD2 (clone 7))

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Normal (average)

  3306. IBBISTi017-A (AS-MD2 (clone Q))

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  3307. IBKMOLi002-A (CACNA1D L271H iPCs)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Autism spectrum disorder

    Disease:

    Obsolete_hyperinsulinemic hypoglycemia

    Disease:

    Primary hyperaldosteronism

    Disease:

    Muscle hypotonia

  3308. IBKMOLi003-A (vEDS COL3A1 Q105* iPSC)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Vascular ehlers-danlos syndrome

  3309. IBKMOLi004-A (sCeAD iPSC)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)

  3310. IBKMOLi005-A (CTRL iPSC)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Normal (average)

  3311. IBKMOLi006-A (GM08399 iPSCs)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Normal (average)

  3312. IBKMOLi007-A (GM03440 iPSCs)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Normal (average)

  3313. IBMSi001-A (IBMS-iPSC-012-12)

    Taiwan Institute of Biomedical Sciences, Academia Sinica (IBMS)
    Disease:

    Obsolete_autosomal dominant polycystic kidney disease

  3314. IBMSi002-A (IBMS-iPSC-013-06)

    Taiwan Institute of Biomedical Sciences, Academia Sinica (IBMS)
    Disease:

    Obsolete_autosomal dominant polycystic kidney disease

  3315. IBMSi003-A (IBMS-iPSC-014-05)

    Taiwan Institute of Biomedical Sciences, Academia Sinica (IBMS)
    Disease:

    Obsolete_autosomal dominant polycystic kidney disease

  3316. IBMSi027-A (IBMS-iPSC-073-01)

    Taiwan Institute of Biomedical Sciences, Academia Sinica (IBMS)
    Disease:

    Wolfram syndrome

  3317. BIONi010-C-65 (BiONI010-C-O16)

    Germany Fraunhofer Institute for Biomedical Engineering IBMT (IBMT)
    Disease:

    Cystic fibrosis

  3318. BIONi010-C-66 (BIONi010-C-N7)

    Germany Fraunhofer Institute for Biomedical Engineering IBMT (IBMT)
    Disease:

    Cystic fibrosis

  3319. IBPi001-A (HPrF iPSCs 20A)

    Czech Republic Institute of Biophysics of the Czech Academy of Sciences (IBP)
    Disease:

    Normal (average)

  3320. IBPi002-A (P71 iPSCs 1)

    Czech Republic Institute of Biophysics of the Czech Academy of Sciences (IBP)
    Disease:

    Obsolete_prostate adenocarcinoma

  3321. IBTCMi001-A (NDC1)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Normal (average)

  3322. IBTCMi002-A (NDC2)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Normal (average)

  3323. IBTCMi003-A (AD1)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Alzheimer's disease

  3324. IBTCMi004-A (AD2)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Alzheimer's disease

  3325. IBTCMi005-A (AD3)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Alzheimer's disease

  3326. IBTCMi006-A (ACNE1)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Acne

  3327. IBTCMi007-A (ACNE2)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Acne

  3328. ICANi001-A (CDGEN1.16)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  3329. ICANi001-A-1 (CDGEN1.16.40.5)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  3330. ICANi002-A (ICAN-403.3)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal (average)

  3331. ICANi002-A-1 (ICAN-FLNC42.1)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal (average)

  3332. ICANi002-A-2 (SCN5A-Clone 5)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal (average)

  3333. ICANi002-A-3 (ICAN-BAG3-V468MC34)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Dilated cardiomyopathy 1hh

  3334. ICANi002-A-4 (ICAN_BAG3_M468MC19)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Dilated cardiomyopathy 1hh

  3335. ICANi002-A-5 (ICAN-PKP2-H695-W11)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Arrhythmogenic right ventricular dysplasia 9

  3336. ICANi002-A-6 (ICAN-ENTREP1-KO-5.3.14)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal (average)

  3337. ICGi002-A (DMD1_1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  3338. ICGi002-B (DMD1_4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  3339. ICGi002-C (DMD1_11)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  3340. ICGi003-A (f3SMA3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Spinal muscular atrophy type 3

  3341. ICGi005-A (iSMA40)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 1

  3342. ICGi005-B (iSMA37)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 1

  3343. ICGi006-A (m3SMA13)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 2

  3344. ICGi006-B (m3SMA20)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 2

  3345. ICGi007-A (47Q-3Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  3346. ICGi008-A (m55Alz-9L)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_alzheimer's disease

  3347. ICGi008-B (m55Alz-15L)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_alzheimer's disease

  3348. ICGi009-A (iTAF3-17 and iTAF3del17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  3349. ICGi009-B (iTAF3del37 and iTAF3-37)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  3350. ICGi013-A (iTAF13-26 and iTAF13del26)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  3351. ICGi013-B (iTAF13del27 and iTAF13-27)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  3352. ICGi014-A (2M_iALS)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  3353. ICGi015-A

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3354. ICGi015-B

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3355. ICGi015-B-1 (m6.7pCyto-17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3356. ICGi015-B-2 (m6.7pCyto-21)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3357. ICGi015-B-3 (m6.7pCyto-24)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3358. ICGi016-A (iTaf9-11)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual developmental disorder, autosomal dominant 39

  3359. ICGi017-A (TAF14dup10)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3360. ICGi018-A (iHD38Q-3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  3361. ICGi018-B (iHD38Q-2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  3362. ICGi018-C (iHD38Q-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  3363. ICGi019-A (HCM1f6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3364. ICGi019-B (HCM1f33)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3365. ICGi019-B-1 (HCM1f33-wt119)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3366. ICGi019-B-2 (HCM1f33-wt147)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3367. ICGi020-A (ATP7bIL23f)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Wilson disease

  3368. ICGi020-B (ATP7bIL24f)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Wilson disease

  3369. ICGi021-A (K6-4f)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3370. ICGi021-A-1 (K6-4fpCyto-13)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy

  3371. ICGi021-A-2 (K6-4fpCyto-16)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy

  3372. ICGi021-A-3 (K6-4fpCyto-19)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy

  3373. ICGi022-A (K7-4Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3374. ICGi022-A-1 (SOD1-G128R_K7-4L-f and SOD1-G128R)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3375. ICGi022-A-2 (SOD1-D91A and SOD1-D91A_K7-4Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3376. ICGi022-A-3 (K7-MYBPC3-N515del-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3377. ICGi022-A-4 (K7-MYBPC3-N515del-2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3378. ICGi022-A-5 (K7-MYBPC3-N515del-3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3379. ICGi022-A-6 (K74-AsCas12a-N1-26)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3380. ICGi022-A-7 (K74-AsCas12aY1-17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3381. ICGi022-A-8 (K7-4 T32)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3382. ICGi022-A-9 (K7-4Lf MT21)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3383. ICGi022-A-10 (K7-4Lf MT16)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3384. ICGi022-B (K7-2Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3385. ICGi023-A (PD45-6-1Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3386. ICGi024-A

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Ring chromosome 18 syndrome

  3387. ICGi025-A (iTAF11-4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Developmental delay

  3388. ICGi026-A

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Fragile x syndrome

  3389. ICGi028-A (HCM4fm5.2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3390. ICGi029-A (HCM14fm6.2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3391. ICGi029-A-1 (HCM14-3wt1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3392. ICGi029-A-2 (HCM14-3wt8)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3393. ICGi029-A-3 (HCM14-3wt31)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3394. ICGi030-A (HF2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Wilson disease

  3395. ICGi032-A

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Fragile x syndrome

  3396. ICGi033-A (77Q-17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  3397. ICGi033-B (77Q-9)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  3398. ICGi033-C (77Q-20)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  3399. ICGi034-A (PD30-4-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3400. ICGi034-A-1 (PD30-XBP-RFP-6 and PD30-4-7-XBP-RFP-6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3401. ICGi034-A-2 (PD30-4-7-XBP-RFP-51 and PD30-XBP-RFP-51)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3402. ICGi034-A-3 (PD30-4-7-XBP-RFP-52 and PD30-XBP-RFP-52)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3403. ICGi034-A-4 (PD30-4-7-XBP-RFP-86 and PD30-XBP-RFP-86)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3404. ICGi034-B (PD30-5-16)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3405. ICGi034-C (PD30-5-27)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3406. ICGi034-D (PD30-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3407. ICGi034-E (PD30-3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3408. ICGi035-A (iCS-MAF1-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3409. ICGi035-B (iCS-MAF1-11)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3410. ICGi036-A (FH 1.3.1S)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hyperlipoproteinemia, type iia

  3411. ICGi036-A-1 (FH 1.3.1S_130S5 and 130S5)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hyperlipoproteinemia, type iia

  3412. ICGi037-A (FH 3.2.8T)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hyperlipoproteinemia, type iia

  3413. ICGi038-A (FH 5.1.2Sh)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hyperlipoproteinemia, type iia

  3414. ICGi039-A (PD31-6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3415. ICGi039-B (PD31-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3416. ICGi039-C (PD31-15)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3417. ICGi040-A (iTAF16-3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Infertility

  3418. ICGi042-A (PD12-4Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3419. ICGi042-B (PD12-5Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3420. ICGi042-C (PD12-6Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3421. ICGi043-A (LR-21)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3422. ICGi043-A-1 (LR-21-cytoGRX-3c)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3423. ICGi043-B (LR-2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3424. ICGi043-C (LR-15)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3425. ICGi044-A (PD40-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3426. ICGi044-B (PD40-8)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3427. ICGi044-C (PD40-13)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3428. ICGi045-A (M-5)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Rasopathy

  3429. ICGi046-A (V2-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Rasopathy

  3430. ICGi047-A (ГК10-31 and HC10-31)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3431. ICGi052-A (PD57-6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Frontotemporal dementia

  3432. ICGi052-B (PD57-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Frontotemporal dementia

  3433. ICGi052-B-1 (PD57-7 MT8)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Frontotemporal dementia

  3434. ICGi052-B-2 (PD57-7 MT6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Frontotemporal dementia

  3435. ICGi053-A (PD58-4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3436. ICGi053-B (PD58-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3437. ICGi053-C (PD58-14)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3438. ICGi054-A (PD69-1/1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3439. ICGi054-B (PD69-2/1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3440. ICGi054-C (PD69-4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3441. ICGi054-D (PD69-5)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3442. ICGi057-A (K9-4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3443. ICGi058-A (iP63)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Autism spectrum disorder

  3444. ICGi059-A (iHD46Q7.1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  3445. ICGi060-A (PD92-22)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3446. ICGi060-B (PD92-21)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3447. ICGi060-C (PD92-39)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3448. ICHi001-A (TTNtv-001)

    Italy IRCCS Istituto Clinico Humanitas (ICH)
    Disease:

    Cardiomyopathy, dilated

  3449. ICHi002-A (TTNtv-002)

    Italy IRCCS Istituto Clinico Humanitas (ICH)
    Disease:

    Cardiomyopathy, dilated

  3450. ICHi003-A (TTNtv-003)

    Italy IRCCS Istituto Clinico Humanitas (ICH)
    Disease:

    Cardiomyopathy, dilated

  3451. ICHi004-A (TTNtv-004)

    Italy IRCCS Istituto Clinico Humanitas (ICH)
    Disease:

    Cardiomyopathy, dilated

  3452. ICHi005-A (RYR2_G1885E-HOMO)

    Italy IRCCS Istituto Clinico Humanitas (ICH)
    Disease:

    Left ventricular noncompaction

  3453. ICHi006-A (RYR2_G1885E-HET)

    Italy IRCCS Istituto Clinico Humanitas (ICH)
    Disease:

    Normal (average)

  3454. ICMi001-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3455. ICMi001-B

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3456. ICMi001-C

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3457. ICMi002-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3458. ICMi002-B

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3459. ICMi002-C

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3460. ICMi003-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3461. ICMi003-B

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3462. ICMi003-C

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3463. ICMi004-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3464. ICMi004-B

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3465. ICMi004-C

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3466. ICMi005-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3467. ICMi005-B

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3468. ICMi005-C

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3469. ICMi006-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3470. ICMi006-B

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3471. ICMi006-C

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3472. ICMi007-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3473. ICMi007-B

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3474. ICMi007-C

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3475. ICMi008-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3476. ICMi008-B

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3477. ICMi008-C

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  3478. ICNDXHi001-A

    China Innovation Center for Neurological Disorders, Xuanwu Hospital, National Clinical Research Center for Geriatric Diseases (ICNDXH)
    Disease:

    Frontotemporal dementia

  3479. ICSSUi002-A

    China Institute for Cardiovascular Science of Soochow University (ICSSU)
    Disease:

    Aortic dissection

  3480. ICSSUi004-A

    China Institute for Cardiovascular Science of Soochow University (ICSSU)
    Disease:

    Restrictive cardiomyopathy

  3481. ICSSUi005-A

    China Institute for Cardiovascular Science of Soochow University (ICSSU)
    Disease:

    Maternally-inherited diabetes and deafness

  3482. ICSSUi006-A

    China Institute for Cardiovascular Science of Soochow University (ICSSU)
    Disease:

    Dilated cardiomyopathy

  3483. IDIBGIi001-A (GPG1-C23)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Normal (average)

  3484. IDIBGIi002-A (RB20234)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Brugada syndrome

  3485. IDIBGIi003-A (​RB20235)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Brugada syndrome

  3486. IDIBGIi004-A (RB20236)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Brugada syndrome

  3487. IDIBGIi005-A (RB20237)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Normal (average)

  3488. IDIBGIi006-A (CPVT FiPS 51 EP6F-1 and RB20651)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3489. IDIBGIi007-A (RB20652 and CPVT FiPS 52 EP6F-8)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3490. IDIBGIi008-A (RB20653 and CPVT FiPS 53 EP6F-4)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3491. IDIBGIi009-A (RB20654 and CPVT FiPS 54 EP6F-6)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3492. IDIBGIi010-A (RB20655 and ​CPVT FiPS 55 EP6F-8)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Normal (average)

  3493. IDISi001-A

    Spain Health Research Institute of Santiago de Compostela (IDIS)
    Disease:

    Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy

  3494. IDMi001-A (K40)

    Germany Institute for Diabetes Research and Metabolic Diseases (IDM)
    Disease:

    Prediabetes syndrome

  3495. HMGUi001-A-4 (hiPSC-ARX-T2A-H2B-CFP-Flag)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3496. HMGUi001-A-5 (ΔINK4 T2D risk region hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3497. HMGUi001-A-8 (C-PEP-mCherry-hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3498. HMGUi001-A-42 (NEUROD2 nVenus/nVenus iPSCs)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3499. HMGUi001-A-43 (hINS-T2A-H2B-Cherry (-/-), hiPSC-INS-T2A-H2B-Cherry reporter and INSCherry/Cherry)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3500. HMGUi001-A-46 (ARX-CFP/PAX4-mCherry, ARX-T2A-H2B-CFP/H2B-mCherry-RGSHis-T2A-PAX4 and ARXnCFP/nCFP/PAX4mCherry/mCherry)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3501. HMGUi001-A-54 (ARX-T2A-H2B-CFP x C-PEP-mCherry -hiPSC, ARX-CFPxC-PEP-mCherry-hiPSC and ARXCFP/CFP x C-PEPmCherry/+ hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3502. HMGUi001-A-55 (Flattop-T2A-H2B-Venus-hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3503. HMGUi001-A-56 (Flattop-T2A-H2B-VenusxC-Peptide-mCherry-hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3504. HMGUi001-A-61 (SYT13-KOnVenus/nVenus-hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3505. HMGUi001-A-65 (CCKBRΔ12/KO)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3506. HMGUi001-A-67 (CCKBRKO/KO and CCKBRKO H2B-venus KI (C108))

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3507. IDVi001-A (iPS-NR2E3-86)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinitis pigmentosa

  3508. IDVi002-A (iPS-PRPF31-4138)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Normal (average)

  3509. IDVi005-A (hiPSC_5f)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Normal (average)

  3510. IDVi005-A-1 (5F-RHO-P347L-G7)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinitis pigmentosa

  3511. IDVi005-A-2 (5F-RHO-P347L-D8)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinitis pigmentosa

  3512. IDVi006-A (UBAP1L-3225)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinal dystrophy

  3513. IDVi006-A-1 (UBAP1L-3225_CRC2)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinal dystrophy

  3514. IDVi006-A-2 (UBAP1L-3225_CRB22)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinal dystrophy

  3515. IDVi006-A-3 (UBAP1L-3225_CRB112)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinal dystrophy

  3516. IDVi007-A (1U-RHO-P23H-01)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinitis pigmentosa

  3517. IDVi007-A-1 (1U-iso-RHO-D2)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinitis pigmentosa

  3518. IDVi007-A-2 (1U-iso-RHO-G2)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinitis pigmentosa

  3519. IDVi007-A-3 (1U-iso-RHO-H6)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinitis pigmentosa

  3520. IDVi007-B (1U-RHO-P23H-02)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinitis pigmentosa

  3521. IGGi001-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Obsolete sotos syndrome 1

  3522. IGGi001-B

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Obsolete sotos syndrome 1

  3523. IGGi002-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Cystic fibrosis

  3524. IGGi002-B (IPSC CF9 CLONE3)

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Cystic fibrosis

  3525. IGGi003-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Sotos syndrome

  3526. IGGi004-A (ZEB2 case 1)

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Mowat-wilson syndrome

  3527. IGGi005-A (ZEB2 case 2)

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Mowat-wilson syndrome

  3528. IGGi006-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Caprin1

  3529. IGGi007-A (iPSC hNECWT4 CLONE1)

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Normal (average)

  3530. IGGi007-B

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Normal (average)

  3531. IGGi008-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Mowat-wilson syndrome

  3532. IGGi009-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Mowat-wilson syndrome

  3533. IGGi010-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Normal (average)

  3534. IGGi011-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Normal (average)

  3535. IGGi011-B

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Normal (average)

  3536. IGGi012-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Normal (average)

  3537. IGGi013-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Normal (average)

  3538. IGGi016-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Normal (average)

  3539. IGIBi001-A (SCP28)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Sickle cell anemia

  3540. IGIBi002-A

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Beta-thalassemia

  3541. IGIBi011-A (GOC-13)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Spinocerebellar ataxia type 12

  3542. IGIBi012-A (FA-hiPSC_001)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Friedreich ataxia

  3543. IGIBi013-A (FA_hiPSC_002)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Friedreich ataxia

  3544. IGIBi016-A (FA-hiPSC_005)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Friedreich ataxia

  3545. IGIBi017-A (CT_hiPSC_001)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3546. IGIBi018-A

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Rubinstein taybi like syndrome

  3547. IGIBi019-A (iPSC V2b)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3548. IGIBi020-A (iPSC V1b)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3549. IGIBi021-A (iPSC V3b)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3550. IGIBi022-A (iPSC V2c)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3551. IGIBi023-A (iPSC V1c)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3552. IGIBi024-A (iPSC V3c)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3553. IGIBi025-A (iPSC V3a)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3554. IGIBi026-A (BKWD01)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Wilson disease

  3555. IIMCBi003-A (K-Pic1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)
    Disease:

    Normal (average)

  3556. IIMCBi003-B (K-Pic2)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)
    Disease:

    Normal (average)

  3557. IIMCBi004-A (PM-H1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)

  3558. IIMCBi005-A (EM-K3)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)

  3559. IIMCBi006-A (M-T1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)
    Disease:

    Huntington's disease

  3560. IIMCBi006-B (M-T2)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)
    Disease:

    Huntington's disease

  3561. IIMCBi007-A (jK-N1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)
    Disease:

    Normal (average)

  3562. IIMCBi008-A (jHD-V1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)

  3563. IMAGINi002-A (IMAGINE002)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Epidermolysis bullosa

  3564. IMAGINi003-A (IMAGINE003)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Epidermolysis bullosa

  3565. IMAGINi004-A (IMAGINE004)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  3566. IMAGINi005-A (IMAGINE005)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  3567. IMAGINi013-A (IMAGINE013)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  3568. IMAGINi020-A (IMAGINE020)

    France Imagine Institute / INSERM U1163 (IMAGIN)

  3569. IMAGINi021-A (IMAGINE021)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  3570. IMAGINi022-A (IMAGINE022)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Waardenburg syndrome

  3571. IMAGINi039-A (IMAGINE039)

    France Imagine Institute / INSERM U1163 (IMAGIN)

  3572. IMAGINi045-A (IMAGINE045)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Loeys-dietz syndrome

  3573. IMAGINi050-A (IMAGINE050)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Tay-sachs disease

  3574. IMAGINi051-A (IMAGINE051)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Tay-sachs disease

  3575. IMAGINi052-A (IMAGINE052)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Tay-sachs disease

  3576. IMAGINi070-A (IMAGINE070)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Meier-gorlin syndrome 1

  3577. IMBAi001-A (SCCF-176J clone#1 and HD.1 ARID1B+/+ clone 3a (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3578. IMBAi001-A-1 (HD.1 ARID1B+/- clone 3b (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3579. IMBAi001-B (SCCF-176J clone#2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3580. IMBAi002-A (SCCF-177J clone#8)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3581. IMBAi002-B (SCCF-177J clone#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3582. IMBAi002-C (SCCF-177J clone#6)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3583. IMBAi003-A (SCCF-178J clone#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3584. IMBAi003-B (SCCF-178J clone#6)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3585. IMBAi004-A (SCCF-733J clone#1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3586. IMBAi004-B (SCCF-733J clone#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3587. IMBAi004-C (SCCF-733J clone#17)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3588. IMBAi005-A (SCCF-734J clone#2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3589. IMBAi005-B (SCCF-734J clone#3)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3590. IMBAi005-C (SCCF-734J clone#10)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3591. IMBAi006-A (SCCF-735J clone#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3592. IMBAi006-B (SCCF-735J clone#17)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3593. IMBAi006-C (SCCF-735J clone#20)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3594. IMBAi007-A (SCCF-180J clone#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3595. IMBAi007-B (SCCF-180J clone#11)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3596. IMBAi007-C (SCCF-180J clone#21)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3597. IMBAi008-A (SCCF-181J clone#16)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3598. IMBAi008-B (SCCF-181J clone#20)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3599. IMBAi008-C (SCCF-181J clone#24)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3600. IMBAi009-A (SCCF-179J clone#13)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3601. IMBAi009-B (SCCF-179J clone#15)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3602. IMBAi009-C (SCCF-179J clone#18)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3603. IMBAi010-A (SCCF-2298J clone#1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3604. IMBAi010-B (SCCF-2298J clone#2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3605. IMBAi010-C (SCCF-2298J clone#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3606. IMBAi011-A (SCCF-736J clone#1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3607. IMBAi011-B (SCCF-736J clone#6)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3608. IMBAi011-C (SCCF-736J clone#8)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3609. IMBAi012-A (DBA 13j #1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3610. IMBAi013-A (DBA 14J #2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Diamond-blackfan anemia 1

  3611. IMBAi014-A (DBA 15J #3)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Diamond-blackfan anemia 1

  3612. IMBAi015-A (DBA 16J #1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Diamond-blackfan anemia 1

  3613. IMBAi016-A (B001-ARID1B#10 and Pat.1 ARID1B+/- clone 1a (XY))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3614. IMBAi017-A (B002-ARID1B#8 and Pat.2 ARID1B+/- clone 2a (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3615. IMBAi017-A-1 (Pat.2 ARID1B+/+ clone 2c (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3616. IMBAi017-A-2 (Pat.2 ARID1B+/+ clone 2d (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3617. IMBAi017-A-3 (Pat.2 ARID1B+/- clone 2b (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3618. IMBAi018-A (622_DS04 #1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Dravet syndrome

  3619. IMBAi019-A (623_DS22 #10)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Dravet syndrome

  3620. IMBAi020-A (624_DS40 #8)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Dravet syndrome

  3621. IMBAi020-B (624_DS40 #3)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Dravet syndrome

  3622. IMBAi021-A (TSC107J #5 and TSC#14 clone 107J#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  3623. IMBAi022-A (TSC112#4 and TSC#24 clone 112#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  3624. IMBAi022-A-1 (TSC112#4r2c4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  3625. IMBAi023-A (TSC#5 clone 32S and TSCp5#32S)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  3626. IMBAi023-B (TSC#5 clone 30S, TSCp5#30S and TSC98#30S)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  3627. IMBPASi001-A (iPSC-WFS1-#1)

    Poland Institute of Medical Biology of Polish Academy of Sciences (IMBPAS)
    Disease:

    Wolfram syndrome 1

  3628. ISFi001-A-1

    Switzerland Institute of Medical Genetics (IMG)
    Disease:

    Joubert syndrome 5

  3629. ISFi001-A-2

    Switzerland Institute of Medical Genetics (IMG)
    Disease:

    Joubert syndrome

  3630. IMGi003-A (COQ4_Phe146Cys_Cl.1.1)

    Switzerland Institute of Medical Genetics (IMG)
    Disease:

    Primary coenzyme q10 deficiency 7

  3631. IMGTi001-A (iTAF5-29)

    Russia Research Institute of Medical Genetics, TNMRC (IMGT)
    Disease:

    Phelan-mcdermid syndrome

  3632. IMGTi001-B (iTAF5-32)

    Russia Research Institute of Medical Genetics, TNMRC (IMGT)
    Disease:

    Phelan-mcdermid syndrome

  3633. IMGTi003-A (iTAF6-6)

    Russia Research Institute of Medical Genetics, TNMRC (IMGT)
    Disease:

    Ring chromosome 13 syndrome

  3634. IMOi001-A (STGD PBiPS1-SV4F-1)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3635. IMOi002-A (STGD PBiPS2-SV4F-1)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3636. IMOi003-A (STGD PBiPS3-SV4F-10)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3637. IMOi004-A (STGD PBiPS4-SV4F-1)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3638. IMOi005-A (STGD PBiPS5-SV4F-2)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3639. IMOi006-A (STGD PBiPS6-SV4F-2)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3640. IMRi002-A

    Malaysia Institute for Medical Research (IMR)
    Disease:

    Normal (average)

  3641. INDBi001-A (INDB5.2.14)

    Germany Institute for Neuroanatomy and Developmental Biology, University of Tuebingen (INDB)
    Disease:

    Normal (average)

  3642. INDBi002-A

    Germany Institute for Neuroanatomy and Developmental Biology, University of Tuebingen (INDB)
    Disease:

    Normal (average)

  3643. INDBi002-B

    Germany Institute for Neuroanatomy and Developmental Biology, University of Tuebingen (INDB)
    Disease:

    Normal (average)

  3644. INEUi002-A (iPSC-FN2.1, FN2.1 and FN2.1 WT)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Normal (average)

  3645. INEUi002-A-1 (PKP2 S140F)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Cardiomyopathy

  3646. INEUi002-A-2 (PKP2 KO)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Cardiomyopathy

  3647. INEUi002-A-7 (PKG-KO)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Cardiomyopathy

  3648. INEUi003-A (FHL1-T)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Muscular dystrophy

  3649. INEUi004-A (FHL1-V)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Muscular dystrophy

  3650. INEUi005-A (FOXA2S229*-iPSCs)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Non-acquired combined pituitary hormone deficiency

  3651. INEUi006-A (DESS and IV-A hiPSC line)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Normal (average)

  3652. INEUi007-A (IV-B hiPSC line and DESY-HE)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Desminopathy

  3653. INEUi007-A-1 (IV-B-HO hiPSC line and DESY-HO)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Desminopathy

  3654. INEUi008-A (IV-C hiPSC line and DESJ)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Desminopathy

  3655. IRMBi001-A-1 (AD-PS1-ISO1)

    France Institute for Neurosciences of Montpellier (INM)
    Disease:

    Obsolete_alzheimer's disease

  3656. IRMBi001-A-2 (AD-PS1-ISO2)

    France Institute for Neurosciences of Montpellier (INM)
    Disease:

    Obsolete_alzheimer's disease

  3657. INNDSUi001-A (186-Nml-F-24)

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Normal (average)

  3658. INNDSUi002-A (21-013)

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Multiple acyl-coa dehydrogenase deficiency

  3659. INNDSUi003-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Becker muscular dystrophy

  3660. INNDSUi004-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Nemaline myopathy

  3661. INNDSUi005-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Normal (average)

  3662. INNDSUi006-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Myotonic dystrophy type 1

  3663. INNDSUi007-A (ZHH-KD)

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Kennedy disease

  3664. INNDSUi008-A (JKL-SCA)

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Machado-joseph disease

  3665. INNDSUi009-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Amyotrophic lateral sclerosis

  3666. INNDSUi010-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Dermatomyositis

  3667. INNDSUi011-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Peripheral neuropathy

  3668. INSAi001-A

    Portugal Instituto Nacional de Saude Ricardo Jorge (INSA)
    Disease:

    Gaucher disease type 3

  3669. INSAi002-A

    Portugal Instituto Nacional de Saude Ricardo Jorge (INSA)
    Disease:

    Fabry disease

  3670. INSAi003-A

    Portugal Instituto Nacional de Saude Ricardo Jorge (INSA)
    Disease:

    Mucolipidosis type ii

  3671. TMOi001-A-11

    France INSERM (INSRM)
    Disease:

    Cardiomyopathy

  3672. INSRMi002-A (PC117_c2)

    France INSERM (INSRM)
    Disease:

    Obsolete_epilepsy

  3673. INSRMi003-A (PC128_c5)

    France INSERM (INSRM)
    Disease:

    Normal (average)

  3674. INSRMi004-A (PC118_c7)

    France INSERM (INSRM)
    Disease:

    Obsolete_epilepsy

  3675. INSRMi005-A (PC119_c7)

    France INSERM (INSRM)
    Disease:

    Normal (average)

  3676. INSRMi006-A (PC131_c8)

    France INSERM (INSRM)
    Disease:

    Obsolete_epilepsy

  3677. INSRMi007-A (pc132-c4)

    France INSERM (INSRM)
    Disease:

    Normal (average)

  3678. INSRMi012-C (PC173T19)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  3679. INSRMi013-A (PC179c1)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  3680. INSRMi014-A

    France INSERM (INSRM)

  3681. INSRMi015-A

    France INSERM (INSRM)
    Disease:

    Long qt syndrome

  3682. INSRMi019-A (PC129K8)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  3683. INSRMi020-A (PC130k2c)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  3684. INSRMi021-A (PC177 3c14)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  3685. IOBi001-A (F49B7 and 01F49i-N-B7)

    Switzerland Institute of Molecular and Clinical Ophthalmology Basel (IOB) (IOB)
    Disease:

    Normal (average)

  3686. IOCVi002-A (iPSC-FOXE3)

    Mexico Institute of Ophthalmology "Conde de Valenciana" (IOCV)

  3687. IPi001-A (iPSC-healthy-AFC-001)

    France Institut Pasteur (IP)
    Disease:

    Normal (average)

  3688. IPi001-B (iPSC-healthy-AFC-002)

    France Institut Pasteur (IP)
    Disease:

    Normal (average)

  3689. IPi001-C (iPSC-healthy-AFC-003)

    France Institut Pasteur (IP)
    Disease:

    Normal (average)

  3690. IPi002-A (iPSC-MARCH-AFC-001)

    France Institut Pasteur (IP)
    Disease:

    Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome

  3691. IPi002-B (iPSC-MARCH-AFC-002)

    France Institut Pasteur (IP)
    Disease:

    Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome

  3692. IPi002-C (iPSC-MARCH-AFC-003)

    France Institut Pasteur (IP)
    Disease:

    Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome

  3693. IPBi001-A (IPB-HD-001)

    South Korea iPSBIO (IPB)
    Disease:

    Huntington disease

  3694. IPBi002-A (IPB-HD-002)

    South Korea iPSBIO (IPB)
    Disease:

    Huntington disease

  3695. IPBi003-A (IPB-HD-003)

    South Korea iPSBIO (IPB)
    Disease:

    Huntington disease

  3696. IPBi004-A (IPB-HD-004)

    South Korea iPSBIO (IPB)
    Disease:

    Huntington disease

  3697. IPBi101-A (IPB-WT-001)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3698. IPBi102-A (IPB-WT-002)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3699. IPBi103-A (IPB-WT-003)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3700. IPBi104-A (IPB-WT-004-LOY)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3701. IPBi104-B (IPB-WT-004)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3702. IPBi105-A (IPB-WT-005)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3703. IPBi106-A (IPB-WT-006)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3704. IPBi107-A (IPB-WT-007)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3705. IPBi108-A (IPB-WT-008)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3706. IPBi109-A (IPB-WT-009)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3707. IPBi110-A (IPB-WT-010)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3708. IPBi111-A (IPB-WT-011)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3709. IPBi112-A (IPB-WT-012)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3710. IPBi113-A (IPB-WT-013)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3711. IPBi114-A (IPB-WT-014)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3712. IPBi115-A (IPB-WT-015)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3713. IPBi116-A (IPB-WT-016)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3714. IPBi117-A (IPB-WT-017)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3715. IPBi118-A (IPB-WT-018)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3716. IPBi119-A (IPB-WT-019)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3717. IPBi124-A (IPB-WT-024)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3718. IPBi126-A (IPB-WT-026)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3719. IPBi128-A (IPB-WT-028)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3720. IPBi129-A (IPB-WT-029)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3721. IPSCi001-A (IPSC-087-3)

    Taiwan iPSC Core (IPSC)
    Disease:

    Occult macular dystrophy

  3722. IPSCZHi001-A (GM769_S6)

    Switzerland iPSCore Zurich (IPSCZH)
    Disease:

    Periventricular nodular heterotopia

  3723. IPTi001-A (15M0008)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  3724. IPTi002-A (15F0009)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  3725. IPTi003-A (15M0010)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  3726. IPTi004-A (15M0011)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  3727. IPTi005-A (16M0064)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal (average)

  3728. IPTi006-A (16M0065)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal (average)

  3729. IPTi007-A (16F0066)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal (average)

  3730. IRDWCHi001-A

    China Institute of Rare Diseases (IRDWCH)
    Disease:

    Hearing loss

  3731. IRFMNi001-A (iPS clone IV)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal (average)

  3732. CIGLi001-A-8

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal (average)

  3733. IRFMNi001-B (iPS clone XI)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal (average)

  3734. IRFMNi001-B-1 (Clone XI CIITAKO)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal (average)

  3735. IRFMNi001-B-2 (CIone M CIITAKO-B2MKO)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal (average)

  3736. IRFMNi002-A (PRM#14)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  3737. IRFMNi002-B (PRM#18)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  3738. IRFMNi003-A

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal (average)

  3739. IRFMNi003-A-1 (KO PKD2#17)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Obsolete_autosomal dominant polycystic kidney disease

  3740. IRFMNi003-A-2 (KO PKD2#36)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Obsolete_autosomal dominant polycystic kidney disease

  3741. IRFMNi003-A-3 (KO PKD1#16)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Obsolete_autosomal dominant polycystic kidney disease

  3742. IRFMNi003-A-4 (KO PKD1#5)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Obsolete_autosomal dominant polycystic kidney disease

  3743. IRMBi001-A (AD-PS1 hiPSC)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Obsolete_alzheimer's disease

  3744. IRMBi002-A (AD-APP hiPSC)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Obsolete_alzheimer's disease

  3745. IRMBi003-A (CT1)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Normal (average)

  3746. IRMBi003-B

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Normal (average)

  3747. IRMBi004-A (CT4)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Normal (average)

  3748. IRMBi005-A (SAD)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Alzheimer disease

  3749. ISCRMi001-A (3-0062 and DSP Leu462fs)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  3750. UCSFi001-A-1X

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Normal (average)

  3751. ISCRMi002-A (6672.4)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Normal (average)

  3752. ISCRMi004-A (6706.7)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer disease

  3753. ISCRMi005-A (6713.1)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer disease

  3754. ISCRMi006-A (6729.4)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

  3755. ISCRMi007-A (6745.2)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

  3756. ISCRMi008-A (6763.1)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Normal (average)

  3757. ISCRMi009-A (6770.2)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

  3758. ISCRMi010-A (6774.1)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Normal (average)

  3759. ISCRMi011-A (6776.2)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

  3760. ISCRMi012-A (6829.4)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

  3761. ISCRMi013-A (6832.2)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

  3762. ISCRMi014-A (6841.4)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

  3763. ISCRMi015-A (6851.2)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

    Disease:

    Lewy body dementia

  3764. ISCRMi016-A (6859.6)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Normal (average)

  3765. ISCRMi017-A (6862.4)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Normal (average)

  3766. ISCRMi018-A (6868.6)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

  3767. ISCRMi019-A (6874.2)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

    Disease:

    Vascular brain injury

  3768. ISCRMi020-A (6888.2)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

  3769. ISCRMi021-A (6904.1)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Normal (average)

  3770. ISCRMi022-A (6992.4)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Normal (average)

  3771. ISCRMi023-A (7027.2)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

  3772. ISCRMi024-A (7029.22)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Normal (average)

  3773. ISCRMi025-A (7060.12)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Normal (average)

  3774. ISCRMi026-A (7124.2)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Alzheimer's disease

  3775. ISCRMi027-A (7152.2)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Lewy body dementia

  3776. ISCRMi028-A (6674.1)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Lewy body dementia

  3777. ISFi001-A (HMGU1 and #1)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Normal (average)

  3778. ISFi002-A (HMGU12)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Normal (average)

  3779. ISFi003-A (D2)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Van maldergem syndrome 1

  3780. ISFi004-A (F1)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Van maldergem syndrome 1

  3781. ISMMSi001-A (SAMEA104275576 and MFS44-E)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  3782. UCSFi001-A-79 (MSE2336A and WTC11-AAVS1-GCamp6s C1)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3783. ISMMSi001-B (SAMEA104275577 and MFS44-16)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  3784. ISMMSi002-A (SAMEA104275578 and MFS60-12)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  3785. ISMMSi002-B (MFS60-3-1 and SAMEA104276575)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  3786. ISMMSi004-A (MSN01-02S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3787. ISMMSi005-A (MSN02-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3788. ISMMSi006-A (MSN03-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3789. ISMMSi007-A (MSN04-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3790. ISMMSi008-A (MSN05-01R)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3791. ISMMSi009-A (MSN06-07R)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3792. ISMMSi010-A (MSN07-07S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3793. ISMMSi011-A (MSN08-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3794. ISMMSi012-A (MSN09-02S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3795. ISMMSi013-A (MSN10-07S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3796. ISMMSi014-A (MSN11-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3797. ISMMSi015-A (MSN12-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3798. ISMMSi016-A (MSN13-03S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3799. ISMMSi017-A (MSN14-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3800. ISMMSi017-B (MSN14-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3801. ISMMSi017-C (MSN14-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3802. ISMMSi018-A (MSN15-31S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3803. ISMMSi019-A (MSN16-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3804. ISMMSi020-A (MSN17-07S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3805. ISMMSi021-A (MSN18-03S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3806. ISMMSi022-A (MSN19-07S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3807. ISMMSi023-A (MSN20-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3808. ISMMSi024-A (MSN21-08S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3809. ISMMSi025-A (MSN22-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3810. ISMMSi026-A (MSN23-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3811. ISMMSi027-A (MSN24-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3812. ISMMSi028-A (MSN25-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3813. ISMMSi028-B (MSN25-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3814. ISMMSi028-C (MSN25-09S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3815. ISMMSi029-A (MSN26-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3816. ISMMSi030-A (MSN27-03S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3817. ISMMSi031-A (MSN28-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3818. ISMMSi032-A (MSN29-03S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3819. ISMMSi033-A (MSN30-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3820. ISMMSi034-A (MSN31-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3821. ISMMSi035-A (MSN32-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3822. ISMMSi036-A (MSN33-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3823. ISMMSi037-A (MSN34-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3824. ISMMSi038-A (MSN35-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3825. ISMMSi039-A (MSN36-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3826. ISMMSi040-A (MSN37-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3827. ISMMSi041-A (MSN38-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3828. ISMMSi042-A (MSN39-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3829. ISMMSi043-A (MSN40-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3830. ISMMSi044-A (PLNR14del-1BC1)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  3831. ISMMSi045-A (PLNR14del-2BC4)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  3832. ISMMSi046-A (PLN-R14del-3BC7)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  3833. ISMMSi047-A (PLN-R14del-4AC4)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  3834. ISMMSi048-A (PLN-R14del-5BC4)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  3835. ISMMSi049-A (PLN-1CC1)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3836. ISMMSi050-A (PLN-4CC4)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3837. ISMMSi051-A (PLN-5AC2)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3838. ISMMSi060-A (CSI2101A)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Combined oxidative phosphorylation defect type 25

  3839. ISTEMi001-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease type iii

  3840. ISTEMi002-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease type iii

  3841. ISTEMi003-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease type iii

  3842. ISTEMi004-A (CAC1, 7255_clG, 7255cloneG and 7255_CACNA1S-01 cloneG)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Congenital myopathy 18

  3843. ISTEMi005-A (CAC2, 9881-clC and 9881cloneC)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Congenital myopathy 18

  3844. ISTEMi006-A (CAC3, 18169-clAA, 18169cloneAA and 18169_CACNA1S-03 cloneAA)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Congenital myopathy 18

  3845. ISTEMi007-A (CAC4, 19895_clR, 19895_CACNA1S-04 cloneR and 19895cloneR)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Congenital myopathy 18

  3846. ISTEMi008-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease ii

  3847. ISTEMi009-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease ii

  3848. ISTEMi010-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease ii

  3849. ISTEMi011-A (WDR45 BPAN01 c02 and CO-A Cl2)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3850. ISTEMi011-B (WDR45 BPAN01 c09 and CO-A Cl9)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3851. ISTEMi012-A (WDR45 BPAN02 c04 and HE-M Cl4)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3852. ISTEMi013-A (WDR45 BPAN03 c05 and SI-A Cl5)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3853. ISTEMi013-B (WDR45 BPAN03 c12 and SI-A Cl12)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3854. ISTEMi014-A (WDR45 BPAN04 c04 and BT-O cl4)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3855. ISTEMi015-A (4603c53)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Normal (average)

  3856. ISTEMi015-A-1 (4603c53_LC3)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Normal (average)

  3857. ISTEMi016-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Danon disease

  3858. ISTEMi017-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Danon disease

  3859. ISTEMi018-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Duchenne muscular dystrophy

  3860. ISTEMi019-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Duchenne muscular dystrophy

  3861. ISTEMi020-A (PYROXD1B)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Pyroxd1

  3862. ISTEMi021-A (ACTN2)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Congenital myopathy

  3863. ISTEMi022-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Duchenne muscular dystrophy

  3864. ITBi001-A (EP1A)

    Italy Institute for Biomedical Technologies (ITB)
    Disease:

    Developmental and epileptic encephalopathy 85 with or without midline brain defects

  3865. ITBi002-A (EP2B)

    Italy Institute for Biomedical Technologies (ITB)
    Disease:

    Developmental and epileptic encephalopathy 85 with or without midline brain defects

  3866. ITXi001-A (hERG CT Cl9)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3867. ITXi001-A-1 (GPR146KO Cl2)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3868. ITXi002-A (IRX5-Wt and H166Wt C09)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3869. ITXi002-A-1 (CRISPR-2 IRX5 F12 Het and IRX5-Het)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3870. ITXi002-A-2 (CRISPR-2 IRX5 D8 KO and IRX5-KO)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3871. ITXi002-A-3 (IRX5-KI and CRISPR-3 IRX5 F6 KI)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3872. ITXi003-A (MS368)

    France l’institut du thorax (ITX)
    Disease:

    Long qt syndrome

  3873. ITXi004-A (MS381)

    France l’institut du thorax (ITX)
    Disease:

    Long qt syndrome

  3874. ITXi005-A (MS573)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3875. ITXi006-A (WT8288)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3876. ITXi006-A-1 (IM-R406W)

    France l’institut du thorax (ITX)
    Disease:

    Desminopathy

  3877. ITXi007-A (202CT)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3878. ITXi008-A (SD378M)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3879. ITXi009-A (CPVT068)

    France l’institut du thorax (ITX)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3880. ITXi010-A (CPVT249)

    France l’institut du thorax (ITX)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3881. ITXi011-A (CPVT033)

    France l’institut du thorax (ITX)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3882. ITXi012-A (Lp(a) Cl23)

    France l’institut du thorax (ITX)
    Disease:

    Hyperlipoproteinemia

  3883. ITXi013-A (PT-R406W)

    France l’institut du thorax (ITX)
    Disease:

    Desminopathy

  3884. ITXi013-B (IC-R406)

    France l’institut du thorax (ITX)
    Disease:

    Desminopathy

  3885. IUFi002-A

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Leigh syndrome

  3886. WTSIi018-B-19

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Loss of function gene mutation

  3887. WTSIi018-B-20

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Loss of function gene mutation

  3888. WTSIi018-B-28 (DU411)

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Duchenne muscular dystrophy

  3889. WTSIi018-B-29 (DU414)

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Duchenne muscular dystrophy

  3890. WTSIi018-B-30 (DU434)

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Xeroderma pigmentosum group a

  3891. WTSIi018-B-35 (DU545)

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Ichthyosis

    Disease:

    Atopic dermatitis

  3892. WTSIi018-B-36 (DU546)

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Ichthyosis

    Disease:

    Atopic dermatitis

  3893. IUFi020-A (DU372r)

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Autoimmune encephalitis

  3894. WTSIi018-B-12 (KOLF2.1J)

    United Kingdom Jackson Laboratories (JAX)
    Disease:

    Normal (average)

  3895. JHUi005-A (HFD1)

    United States Johns Hopkins University (JHU)
    Disease:

    Marfan syndrome

  3896. JHUi006-A (HFD2 Clone 11)

    United States Johns Hopkins University (JHU)
    Disease:

    Marfan syndrome

  3897. JHUi007-A (i0195, Clone 5)

    United States Johns Hopkins University (JHU)
    Disease:

    Ehlers-danlos syndrome, vascular type

  3898. JHUi007-A-1 (i0195 SubClone D8)

    United States Johns Hopkins University (JHU)
    Disease:

    Ehlers-danlos syndrome, vascular type

  3899. JHUi008-A (JHU001, clone 2)

    United States Johns Hopkins University (JHU)
    Disease:

    Normal (average)

  3900. JHUi009-A (JHU004 Clone 3)

    United States Johns Hopkins University (JHU)
    Disease:

    Ehlers-danlos syndrome, vascular type

  3901. JHUi009-A-1 (JHU004, Clone F6)

    United States Johns Hopkins University (JHU)
    Disease:

    Ehlers-danlos syndrome, vascular type

  3902. JHUi010-A (JHU013, Clone 2)

    United States Johns Hopkins University (JHU)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  3903. JNCHi002-A (JNCHi002-A)

    China Jinan children's Hospital (JNCH)
    Disease:

    Familial hypercholesterolemia

  3904. JNMUi001-A (JNMUi001-A)

    China Jining Medical University (JNMU)
    Disease:

    Schizophrenia

  3905. JNMUi002-A (JNMUi002-A)

    China Jining Medical University (JNMU)
    Disease:

    Schizophrenia

  3906. JNMUi003-A (iPSCs—PB-SCZ-70#-C1P19)

    China Jining Medical University (JNMU)
    Disease:

    Schizophrenia

  3907. JTUi001-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Charge syndrome

  3908. JTUi002-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Waardenburg syndrome

  3909. JTUi003-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Obsolete_otosclerosis

  3910. JTUi004-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Obsolete_otosclerosis

  3911. JTUi005-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Neuronal intranuclear inclusion disease

  3912. JTUi007-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

  3913. JUCGRMi001-A (VPS35A4)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3914. JUCGRMi001-B (VPS35A5)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3915. JUCGRMi001-C (VPS35A8)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3916. JUCGRMi002-A (DupA5)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3917. JUCGRMi002-B (DupA13)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3918. JUCGRMi002-C (DupA18)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3919. JUCGRMi003-A (PH13)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3920. JUCGRMi004-A (CMTA6)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Charcot-marie-tooth disease

  3921. JUCGRMi005-A (JA5)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Normal (average)

  3922. JUCGRMi006-A (JB6)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Normal (average)

  3923. JUCGRMi007-A (MAPTC3)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Frontotemporal dementia

  3924. JUCGRMi007-B (MAPTC5)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Frontotemporal dementia

  3925. JUCGRMi007-C (MAPTC9)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Frontotemporal dementia

  3926. JUCGRMi008-A (WDRC2)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Neurodegeneration with brain iron accumulation

  3927. JUCTCi018-A

    Jordan the University of Jordan / Cell Therapy center (JUCTC)
    Disease:

    Charcot-marie-tooth disease

  3928. JUCTCi019-A

    Jordan the University of Jordan / Cell Therapy center (JUCTC)
    Disease:

    Charcot-marie-tooth disease type 2

  3929. JUFMDOi007-A

    Japan Juntendo University Faculty of Medicine, Department of Otorhinolaryngology (JUFMDO)
    Disease:

    Ush2a

  3930. JUFMDOi008-A (CP009)

    Japan Juntendo University Faculty of Medicine, Department of Otorhinolaryngology (JUFMDO)
    Disease:

    Autosomal recessive nonsyndromic deafness 12

  3931. KAIMRCi002-A (HLA-iPSC#1)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Normal (average)

  3932. KAIMRCi002-B (HLA-iPSC#2)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Normal (average)

  3933. KAIMRCi003-A (DRVT-iPSC#1)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Dravet syndrome

  3934. KAIMRCi003-B (DRVT-iPSC#2)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Dravet syndrome

  3935. KAIMRCi004-A (BTBGD-iPSC#1)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Biotin-thiamine-responsive basal ganglia disease

  3936. KAIMRCi004-B (BTBGD-iPSC#2)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Biotin-thiamine-responsive basal ganglia disease

  3937. KAIMRCi010-A (LQTS-iPSC#1)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Long qt syndrome

  3938. KAIMRCi010-B (LQTS-iPSC#2)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Long qt syndrome

  3939. KAIMRCi011-A (LQTS-WT-iPSC#1)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Normal (average)

  3940. KAIMRCi011-B (LQTS-WT-iPSC#2)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Normal (average)

  3941. KAIMRCi019-A (HLA2-iPSC#1)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Normal (average)

  3942. KAIMRCi019-B

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Normal (average)

  3943. KAUSTi001-A (KS7-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3944. KAUSTi001-B (KS7-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3945. KAUSTi003-A (KS1-iPSC#D)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3946. KAUSTi004-A (HM-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  3947. KAUSTi004-B (HM-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  3948. KAUSTi005-A (HB-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  3949. KAUSTi005-B (HB-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  3950. KAUSTi005-C (HB-iPSC#C)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  3951. KAUSTi006-A (KS6-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3952. KAUSTi006-B (KS6-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3953. KAUSTi007-A (KS2-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3954. KAUSTi007-B (KS2-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3955. KAUSTi008-A (KS4-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3956. KAUSTi008-B (KS4-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3957. KAUSTi008-C (KS4-iPSC#C)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3958. KAUSTi008-D (KS4-iPSC#D)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3959. KAUSTi008-E (KS4-iPSC#E)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3960. KAUSTi008-F (KS4-iPSC#F)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3961. KAUSTi008-G (KS4-iPSC#G)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3962. KAUSTi009-A (KS3-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3963. KAUSTi009-B (KS3-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3964. KAUSTi010-A (KS5-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3965. KAUSTi010-B (KS5-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Obsolete_klinefelter's syndrome

  3966. KAUSTi011-A (iPSC-GLP1R-KO-C1)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Developmental and epileptic encephalopathy

  3967. KAUSTi011-B (iPSC-GLP1R-KO-H4)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Developmental and epileptic encephalopathy

  3968. KCGMHi001-A (KCGMH-CEP85L-K303-A4)

    Taiwan Kaohsiung Chang Gung Memorial Hospital (KCGMH)
    Disease:

    Lissencephaly

  3969. KCGMHi002-A (KCGMH-MAST1-K2271-A1)

    Taiwan Kaohsiung Chang Gung Memorial Hospital (KCGMH)
    Disease:

    Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations

  3970. KCGMHi003-A (KCGMH-SCA8-K3143-A4)

    Taiwan Kaohsiung Chang Gung Memorial Hospital (KCGMH)
    Disease:

    Spinocerebellar ataxia type 8

  3971. KCLi001-A (iOP118)

    United Kingdom King's College London (KCL)
    Disease:

    Obsolete_atopic eczema

  3972. KCLi002-A (iOP107)

    United Kingdom King's College London (KCL)
    Disease:

    Obsolete_atopic eczema

  3973. KCLi003-A (iOP101)

    United Kingdom King's College London (KCL)
    Disease:

    Obsolete_atopic eczema

  3974. KEIOi001-A (SM4-4-5)

    Japan Keio University (KEIO)
    Disease:

    Amyotrophic lateral sclerosis type 10

  3975. KEIOi005-A (KAD-0001 and EK-0076)

    Japan Keio University (KEIO)
    Disease:

    Alzheimer's disease

  3976. KEIOi006-A (RPC771-EA)

    Japan Keio University (KEIO)
    Disease:

    Normal (average)

  3977. KEIUi002-A (KOMENT-A)

    Japan Keio University (KEIU)
    Disease:

    Normal (average)

  3978. KEIUi003-A (KOMENT-B)

    Japan Keio University (KEIU)
    Disease:

    Normal (average)

  3979. KEIUi004-A (EYA4-1)

    Japan Keio University (KEIU)
    Disease:

    Hearing loss

  3980. KEIUi005-A (EYA4-2)

    Japan Keio University (KEIU)
    Disease:

    Hearing loss

  3981. KEIUi006-A (EYA4-3)

    Japan Keio University (KEIU)
    Disease:

    Hearing loss

  3982. KEIUi007-A (EYA4-4)

    Japan Keio University (KEIU)
    Disease:

    Hearing loss

  3983. KEIUi008-A (A1555G)

    Japan Keio University (KEIU)
    Disease:

    Hearing loss

  3984. KGUi001-A (AR1023)

    Germany Department of Psychiatry, Psychotherapy and Psychosomatic Medicine, University Hospital, Goethe University of Frankfurt/Main (KGU)
    Disease:

    Obsolete_bipolar disorder

  3985. KGUi002-A (AR1034)

    Germany Department of Psychiatry, Psychotherapy and Psychosomatic Medicine, University Hospital, Goethe University of Frankfurt/Main (KGU)
    Disease:

    Obsolete_bipolar disorder

  3986. KKUi002-A (PD-iPSC)

    South Korea School of medicine, Konkuk University (KKU)
    Disease:

    Normal (average)

  3987. KLRMMEi001-A

    China Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University. (KLRMME)
    Disease:

    Retinitis pigmentosa

  3988. KLRMMEi002-A

    China Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University. (KLRMME)
    Disease:

    Usher syndrome

  3989. KLRMMEi003-A

    China Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University. (KLRMME)
    Disease:

    Usher syndrome

  3990. KMUGMCi001-A (KMUGMCi001ACVRL1)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic

  3991. KMUGMCi002-A (KMUGMCi002NIPBL)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Cornelia de lange syndrome

  3992. KMUGMCi003-A (KMUGMCi003ERCC2 and KN610)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Trichothiodystrophy 1, photosensitive

  3993. KMUGMCi004-A (KMUGMCi004APC and KN615)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Familial adenomatous polyposis

  3994. KMUGMCi005-A (KMUGMCi005TMC8 and KN627)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Epidermodysplasia verruciformis

  3995. KMUGMCi006-A (TS271 #12 WT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  3996. KMUGMCi006-B (TS271 #5 MT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  3997. KMUGMCi006-C (TS271 #21 WT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  3998. KMUGMCi006-D (TS271 #23 WT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  3999. KMUGMCi006-E (TS271 #4 MT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  4000. KMUGMCi006-F (TS271 #20 MT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  4001. KMUGMCi007-A (KMUGMCi007PEPD and KN649)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Prolidase deficiency

  4002. KMUGMCi008-A (KN695 KAT6B and KN695)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Ohdo syndrome

  4003. KMUGMCi009-A (KN686 and KN686 MED12)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Blepharophimosis - intellectual disability syndrome, mkb type

  4004. KMUGMCi010-A (KN687B and KN687B MED12)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Blepharophimosis - intellectual disability syndrome, mkb type

  4005. KRIBBi005-A (CB-iPS-C7)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    Normal (average)

  4006. KRIBBi009-A (KRIBB-BC15)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    Normal (average)

  4007. KRIBBi010-A (XLRS_R141C)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    X-linked retinoschisis

  4008. KRIBBi011-A (XLRS_G44fs)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    X-linked retinoschisis

  4009. KRIBBi012-A (XLRS_E72K)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    X-linked retinoschisis

  4010. KSCBi001-A (hUSiPS2)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4011. KSCBi002-A (hFSiPS1)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4012. KSCBi002-B (hFmiPS1)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4013. KSCBi002-B-1 (hFmiPS2)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4014. KSCBi003-A (hAdMSiPS1 and hAdMSCiPS1)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4015. KSCBi005-A (CMC-hiPSC-003)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4016. KSCBi005-A-1 (CMC-hiPSC-003(Nestin-GFP) and CMC-003i-Nestin.EGFP)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4017. KSCBi005-A-2 (CMC-hiPSC-003(Sox1-GFP) and CMC-003i-Sox1.EGFP)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4018. KSCBi005-A-3 (CMC-003i-Pdx1.EGFP and CMC-hiPSC-003(PDX1-GFP))

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4019. KSCBi005-A-7

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4020. KSCBi006-A (KNIH-OI001i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Osteogenesis imperfecta type 1

  4021. KSCBi007-A (KNIH-PWS001i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Prader-willi syndrome

  4022. KSCBi010-A (DKH005i-A and DKHi005-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Senior-loken syndrome

  4023. KSCBi011-A (DKHi090-A and DKH090i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Leber congenital amaurosis

  4024. KSCBi012-A (NU01-EiPS07)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4025. KSCBi016-A (LQT06-hiPSC, DPHCi06 and KNIH-LQT6-hiPSC)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Long qt syndrome

  4026. KSCBi017-A (PB01-EiPS21)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4027. KSCBi017-A-1 (PB01-EiPS21_GATA6-EGFP)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4028. KSCBi017-A-2

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4029. KSCBi017-A-4

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  4030. KSCBi024-A (Down syndrome-EiPSC)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Down syndrome

  4031. KSCBi025-A (DPHKi08 and KNIH-LQT37-hiPSC)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Brugada syndrome

  4032. KSCBi026-A (KNIH-LQT13-hiPSC, DPHCi13 and LQT-13)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Atrial fibrillation

  4033. BIONi010-C-56 (BIONi010-C-A713T-C25)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  4034. BIONi010-C-57 (BIONi010-C-A713T-C42)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  4035. BIONi010-C-58 (BIONi010-C-A713T-C1)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  4036. BIONi010-C-59 (BIONi010-C-A713T-C33)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  4037. BIONi010-C-60 (BIONi010-C-R589C-C7)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  4038. BIONi010-C-61 (BIONi010-C-R589C-C16)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  4039. BIONi010-C-62 (BIONi010-C-R589C-C5)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  4040. BIONi010-C-63 (BIONi010-C-R589C-C9)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  4041. KUi012-A (JM09)

    Denmark University of Copenhagen (KU)
    Disease:

    Normal (average)

  4042. KUi012-A-1 (JM09 GC)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  4043. KUi013-A (SK)

    Denmark University of Copenhagen (KU)
    Disease:

    Normal (average)

  4044. KUi013-A-1 (SK GC)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  4045. KUCFRi005-A

    South Korea Korea University Cell Function Regulation Lab (KUCFR)
    Disease:

    Normal (average)

  4046. KUCFRi005-A-1

    South Korea Korea University Cell Function Regulation Lab (KUCFR)
    Disease:

    African swine fever virus

  4047. KUIFMSi004-A (201B1)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal (average)

  4048. KUIFMSi004-B (201B6)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal (average)

  4049. KUIFMSi004-C (201B7)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal (average)

  4050. KUIFMSi004-D (201B2)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal (average)

  4051. KUIFMSi004-E (201B3)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal (average)

  4052. KUIFMSi009-A (243H1)

    Japan Kyoto University (KUIMS)

  4053. KUIFMSi009-B (243H7)

    Japan Kyoto University (KUIMS)

  4054. KUIFMSi011-A (246G1)

    Japan Kyoto University (KUIMS)

  4055. KUIFMSi011-B (246G3)

    Japan Kyoto University (KUIMS)

  4056. KUIFMSi011-C (246G4)

    Japan Kyoto University (KUIMS)

  4057. KUIFMSi011-D (246G5)

    Japan Kyoto University (KUIMS)

  4058. KUIFMSi011-E (246G6)

    Japan Kyoto University (KUIMS)

  4059. SIGi001-A-21 (SIGi001-AAVS1-FRT)

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  4060. SIGi001-A-22 (SIGi001-ICAM1-GFP)

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  4061. SIGi001-A-23 (SIGi001-HC3x)

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  4062. SIGi001-A-24 (SIGi001-HC3x-ICAM1-GFP)

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  4063. SIGi001-A-25

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  4064. SIGi001-A-26

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  4065. KULi003-A

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  4066. KULi004-A (SPRED1_01_cln11_UC)

    Belgium KU Leuven (KUL)
    Disease:

    Legius syndrome

  4067. KULi004-B (SPRED1_01_cln11.5.E3)

    Belgium KU Leuven (KUL)
    Disease:

    Legius syndrome

  4068. KULi005-A (SPRED1_02_cln10_UC)

    Belgium KU Leuven (KUL)
    Disease:

    Legius syndrome

  4069. KULi005-B (SPRED1_02_cln18.2_GC)

    Belgium KU Leuven (KUL)
    Disease:

    Legius syndrome

  4070. KULi006-A (SPRED1_04_cln9_UC)

    Belgium KU Leuven (KUL)
    Disease:

    Legius syndrome

  4071. KULi006-B (SPRED1_04_cln9.8.18_GC)

    Belgium KU Leuven (KUL)
    Disease:

    Legius syndrome

  4072. KULi007-A (SPRED1_05_cln3_UC)

    Belgium KU Leuven (KUL)
    Disease:

    Legius syndrome

  4073. KULi007-B (SPRED1_05_cln3.33_GC)

    Belgium KU Leuven (KUL)
    Disease:

    Legius syndrome

  4074. KUMi001-A (KUMi001-A_CML(Ph+))

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Myeloid leukemia, philadelphia-positive

  4075. KUMi002-A (CD34+ CML (Ph-) hiPSCs)

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Chronic myeloid leukemia

  4076. KUMi003-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Obsolete_acute promyelocytic leukemia

  4077. KUMi004-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Chronic lymphocytic leukemia

  4078. KUMi005-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Obsolete_multiple myeloma

  4079. KUMi006-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Obsolete_multiple myeloma

  4080. KUMCi001-A (ALLCD34+)

    South Korea KOREA UNIVERSTY COLLEGE OF MEDICINE (KUMC)
    Disease:

    Acute lymphoblastic leukemia

  4081. KUMCi002-A (MM_CD34+iPSCs)

    South Korea KOREA UNIVERSTY COLLEGE OF MEDICINE (KUMC)
    Disease:

    Obsolete_multiple myeloma

  4082. LBi001-A (PH-BL-001 Clone 4 and iLB-268bfs4)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4083. LBi001-B (iLB-268bfs9 and PH-BL-001 Clone 9)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4084. LBi002-A (PH-BL-002 Clone 2 and iLB-272bfs2)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4085. LBi002-B (PH-BL-002 Clone 9 and iLB-272bfs9)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4086. LBi003-A (iLB-273bms57 and PH-BL-003 Clone 57)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4087. LBi003-B (PH-BL-003 Clone 61 and iLB-273bms61)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4088. LBi004-A (PH-BL-204 Clone 210 and iLB-278bfs210)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4089. LBi004-B (PH-BL-204 Clone 211 and iLB-278bfs211)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4090. LBi005-A (iLB-293bms257 and PH-BL-411 Clone 257)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4091. LBi005-B (iLB-293bms258 and PH-BL-411 Clone 258)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4092. LBi006-A (PH-BL-102 Clone 16 and iLB-269bms16)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4093. LBi006-B (iLB-269bms8 and PH-BL-102 Clone 8)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4094. LBi007-A (iLB-285bfs98 and PH-BL-406 Clone 98)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4095. LBi007-B (iLB-285bfs99 and PH-BL-406 Clone 99)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4096. LBi008-A (PH-BL-407 Clone 128 and iLB-289bms128)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4097. LBi008-B (iLB-289bms145 and PH-BL-407 Clone 145)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4098. LBi009-A (PH-BL-405 Clone 174 and iLB-284bms174)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4099. LBi009-B (iLB-284bms179 and PH-BL-405 Clone 179)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4100. LBi010-A (PH-BL-403 Clone 275 and iLB-282bfs275)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4101. LBi010-B (iLB-282bfs283 and PH-BL-403 Clone 283)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4102. LBi011-A (PH-BL-004 Clone 14 and iLB-274bfs14)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4103. LBi011-B (PH-BL-004 Clone 17 and iLB-274bfs17)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4104. LBi012-A (iLB-292bms74 and PH-BL-410 Clone 74)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4105. LBi012-B (PH-BL-410 Clone 80 and iLB-292bms80)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4106. LBi013-A (PH-BL-304 Clone 117 and iLB-279bfs117)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4107. LBi014-A (iLB-281bfs191 and PH-BL-402 Clone 191)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4108. LBi014-B (PH-BL-402 Clone 192 and iLB-281bfs192)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4109. LBi015-A (iLB-277bms227 and PH-BL-303 Clone 227)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4110. LBi015-B (iLB-277bms234 and PH-BL-303 Clone 234)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4111. LBi016-A (PH-BL-414 Clone 10 and iLB-296bfs10)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4112. LBi016-B (PH-BL-414 Clone 16 and iLB-296bfs16)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4113. LBi017-A (PH-BL-401 Clone 22 and iLB-280bfs22)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4114. LBi017-B (PH-BL-401 Clone 36 and iLB-280bfs36)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4115. LBi018-A (PH-BL-409 Clone 43 and iLB-291bfs43)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4116. LBi018-B (PH-BL-409 Clone 45 and iLB-291bfs45)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4117. LBi019-A (PH-BL-901 Clone 154 and iLB-275bms154)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4118. LBi019-B (iLB-275bms162 and PH-BL-901 Clone 162)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4119. LBi020-A (iLB-294bms22 and PH-BL-412 Clone 238)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  4120. LBMi001-A (idic(Y))

    China Dongfang Hospital of Xiamen University (LBM)
    Disease:

    Infertility

  4121. LCPHi001-A

    China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)
    Disease:

    Obsolete_parkinson's disease

  4122. LCPHi002-A

    China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)
    Disease:

    Parkinson disease

  4123. LCPHi003-A

    China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)
    Disease:

    Parkinson disease

  4124. LCSBi001-A (VPS35 1_2)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Obsolete_parkinson's disease

  4125. LCSBi001-A-2

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Obsolete_parkinson's disease

  4126. LCSBi001-A-3

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Obsolete_parkinson's disease

  4127. LCSBi002-B (ND40066-clone 7 and ND40066-PINK1/PARK6-ILE368ASN-clone 7)

    United States Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4128. LCSBi002-C (ND40066-clone 8 and ND40066-PINK1/PARK6-ILE368ASN-clone 8)

    United States Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4129. LCSBi004-A (ND29369-clone 1 and ND29369-PARKIN/PRKN/PARK2-R275W-clone 1)

    United States Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4130. LCSBi004-B (ND29369-PARKIN/PRKN/PARK2-R275W-clone 4, ND29369-clone 4, ND29369-4 and LCSBi004-B)

    United States Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4131. LCSBi008-A (delP and DJ-1-delP)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4132. LCSBi008-A-1 (delP GC13 and DJ-1-delP GC13)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4133. LCSBi009-A (RHOT1_R272Q_clone1_PD)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4134. LCSBi009-A-1 (RHOT1_R272Q_clone18_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4135. LCSBi010-A (RHOT1_R450C_clone5_PD)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4136. LCSBi010-A-1 (RHOT1_R450C_clone6_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4137. LCSBi010-A-2 (RHOT1_R450C_clone10_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4138. LCSBi011-A (RHOT1_T351A_clone1_PD)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4139. LCSBi011-A-1 (RHOT1_T351A_clone25.2_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4140. LCSBi012-A (RHOT1_T610A_clone6_PD)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4141. LCSBi012-A-1 (RHOT1_T610A_clone62.19.37_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4142. LCSBi013-A (GL2)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4143. LCSBi014-A (#89739 and S1 Cl19a)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4144. LCSBi015-A (S2 Cl4 and 89732)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4145. LCSBi016-A (S3 Cl17 and 90812)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4146. LCSBi017-A (M1 Cl6b and #89721)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4147. LCSBi018-A (M2 Cl4 and #90806)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  4148. LEIi004-A

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  4149. LEIi004-A-1

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  4150. LEIi005-A

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  4151. LEIi006-A

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  4152. LEIi019-A (1020ips3)

    Australia Lions Eye Institute (LEI)
    Disease:

    Pattern dystrophy

  4153. LEIi020-A (1049ips2)

    Australia Lions Eye Institute (LEI)
    Disease:

    Usher syndrome type 1b

  4154. LEIi020-B

    Australia Lions Eye Institute (LEI)
    Disease:

    Usher syndrome type 1b

  4155. LEIi021-A (1577ips7)

    Australia Lions Eye Institute (LEI)
    Disease:

    Normal (average)

  4156. LEIi021-B (1577ips9)

    Australia Lions Eye Institute (LEI)
    Disease:

    Normal (average)

  4157. LEIi022-A (CMRIi0032-A-1 and 1765ips1)

    Australia Lions Eye Institute (LEI)
    Disease:

    Normal (average)

  4158. LEIi022-B (1765ips2 and CMRIi0032-A-2)

    Australia Lions Eye Institute (LEI)
    Disease:

    Normal (average)

  4159. LEIi023-A (1150ips4)

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa 11

  4160. LGMi001-A (ALMS1-STBG-1)

    France Medical Genetics Laboratory (LGM)
    Disease:

    Alstrom syndrome

  4161. LGMi002-A (iPSC-BBS5stbg1)

    France Medical Genetics Laboratory (LGM)
    Disease:

    Bardet-biedl syndrome

  4162. LIBDi020-A (4001.02)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4163. LIBDi021-A (4002.04)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4164. LIBDi022-A (4003.07)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4165. LIBDi023-A (4004.04)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4166. LIBDi024-A (4005.03)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4167. LIBDi025-A (4006.02)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4168. LIBDi026-A (4007.07)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4169. LIBDi027-A (4008.02)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4170. LIMFRi001-A (LIMFR-A)

    France University of Limoges (LIMFR)
    Disease:

    Normal (average)

  4171. LINi001-A (Linea 1)

    Canada LineaBio (LIN)
    Disease:

    Normal (average)

  4172. LNDWCHi001-A (LNDWCH-iPS-PD-PLA2G6–001)

    China Laboratory of Neurodegenerative Disorders (LNDWCH)
    Disease:

    Parkinson disease

  4173. LNRCUi001-A

    United Kingdom Laboratories for Neuroscience Research, Cardiff University (LNRCU)
    Disease:

    Obsessive-compulsive personality disorder

    Disease:

    Phobia

  4174. LNRCUi002-A

    United Kingdom Laboratories for Neuroscience Research, Cardiff University (LNRCU)
    Disease:

    Avoidant personality disorder

    Disease:

    Autism spectrum disorder

  4175. LNRCUi003-A

    United Kingdom Laboratories for Neuroscience Research, Cardiff University (LNRCU)
    Disease:

    Autism spectrum disorder

    Disease:

    Intellectual disability

  4176. LNRCUi004-A

    United Kingdom Laboratories for Neuroscience Research, Cardiff University (LNRCU)
    Disease:

    Major depressive disorder

  4177. LSCTRi006-A (LSCTR-LiPSC-4 and i4)

    South Korea Laboratory of Stem Cells and Tissue Regeneration (LSCTR)
    Disease:

    Normal (average)

  4178. LSCTRi007-A (LSCTR-LiPSC-5 and i5)

    South Korea Laboratory of Stem Cells and Tissue Regeneration (LSCTR)
    Disease:

    Normal (average)

  4179. UCSFi001-A-72 (FUS-R521G HET 2B10 and LSUHSi004-A-72)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  4180. UCSFi001-A-73 (FUS-R521G HOM 1D9)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  4181. UCSFi001-A-74 (FUS-P525L HET 2D1)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  4182. UCSFi001-A-75 (FUS-P525L HOM 2D2)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  4183. LUi001-A (CALP1.3)

    Latvia University of Latvia (LU)
    Disease:

    Calpain-3-related limb-girdle muscular dystrophy r1

  4184. LUi002-A (CALP2.2)

    Latvia University of Latvia (LU)
    Disease:

    Calpain-3-related limb-girdle muscular dystrophy r1

  4185. LUi003-A (CALP3.1)

    Latvia University of Latvia (LU)
    Disease:

    Calpain-3-related limb-girdle muscular dystrophy r1

  4186. LUBi001-A (PGRN-8310, PGRN8310, RCi195 and RCFB58 c12.5)

    Denmark H. Lundbeck A/S (LUB)
    Disease:

    Frontotemporal dementia

  4187. LUBi001-B (PGRN-8310, RCFB58 c4.4, PGRN8310 and RCi194)

    Denmark H. Lundbeck A/S (LUB)
    Disease:

    Frontotemporal dementia

  4188. LUBi001-C (PGRN-8310, RCFB58 c3.7, RCi200 and PGRN8310)

    Denmark H. Lundbeck A/S (LUB)
    Disease:

    Frontotemporal dementia

  4189. LUEi012-A (iPS-L-2131)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Normal (average)

  4190. LUEi013-A (iPS-L-2135)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Normal (average)

  4191. LUEi014-A (iPS-B-125)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Parkinson disease

  4192. LUEi015-A (iPS-B-11)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Parkinson disease

  4193. LUEi017-A (iPS-L-2122)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Parkinson disease

  4194. LUEi018-A (iPS-L-2124)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Parkinson disease

  4195. LUEi019-A (iPS-L-8172-1)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  4196. LUEi019-B (iPS-L-8172-2)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  4197. LUEi020-A (iPS-L9827-6)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  4198. LUEi020-A-1 (iPS-L9827-6_TOR1A_WT-3xFLAG/dGAG)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  4199. LUEi020-A-2 (iPS-L9827-6_TOR1A_WT-3xFLAG/WT-3xFLAG)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  4200. LUEi020-A-3 (iPS-L9827-6_TOR1A_dGAG-3xFLAG/dGAG)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  4201. LUEi020-A-4 (iPS-L9827-6_TOR1A_WT/dGAG-3xFLAG)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  4202. LUMCi001-A (LUMC0054iCTRL02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4203. LUMCi001-B (LUMC0054iCTRL03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4204. LUMCi002-A (113-6 and LUMC0113iATAX06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4205. LUMCi002-B (113-7 and LUMC0113iATAX07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4206. LUMCi002-C (113-8 and LUMC0113iATAX08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4207. LUMCi003-A (114-1 and LUMC0114iCTRL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4208. CRMi003-A-2

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4209. CRMi003-A-3 (Proliving and GMNN-mScarletI Reporter)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4210. LUMCi003-B (114-2 and LUMC0114iCTRL02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4211. LUMCi004-A (LUMC0099iCTRL04)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4212. LUMCi004-A-1 (LU99_AAVS1-bxb-v2)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4213. LUMCi004-A-2 (LU99_CLYBL-bxb-v2)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4214. LUMCi004-A-3 (LUMCi099_XPA_B8)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Xeroderma pigmentosum group a

  4215. LUMCi004-A-4 (LUMCi099_XPC_D10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Xeroderma pigmentosum group c

  4216. LUMCi004-A-5 (LU99_SCN5A-R282H_cis)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Brugada syndrome

  4217. LUMCi004-A-6 (LU99_SCN5A-R282H_trans)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Brugada syndrome

  4218. LUMCi004-A-7 (LU99-04_AAVS-bxb-dual)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4219. LUMCi004-A-8 (LU99 CLYBL-Bxb-v3_Dual and LUMC0099iCLYBL-06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4220. LUMCi004-B (LUMC0030iCTRL12)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4221. LUMCi004-C (LUMC0031iCTRL08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4222. LUMCi004-D (LUMC0289iCTRL07, LUMC0289iCTRL10 and LUMC0289iCTRL12)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4223. LUMCi007-A (LUMC0151iHD01 and 151-1)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  4224. LUMCi007-B (LUMC0151iHD05 and 151-5)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  4225. LUMCi008-A (152-2 and LUMC0152iHD02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  4226. LUMCi008-B (152-3 and LUMC0152iHD03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  4227. LUMCi008-C (152-4 and LUMC0152iHD04)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  4228. LUMCi013-A (LUMC0133iCTRL06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4229. LUMCi014-A (LUMC0134iCTRL29)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4230. LUMCi015-A (LUMC0135iCTRL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4231. LUMCi016-A (LUMC0136iCTRL09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4232. LUMCi017-A (LUMC0111iALK and LUMC0111iALK07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4233. LUMCi017-A-1 (iso01LUMC0111iALK07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4234. LUMCi017-A-2 (iso02LUMC0111iALK07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4235. LUMCi018-A (LUMC0112iALK and LUMC0112iALK08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4236. LUMCi018-A-1 (iso01LUMC0112iALK08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4237. LUMCi018-A-2 (iso02LUMC0112iALK08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4238. LUMCi022-A (115-1 and LUMC0115iATAX01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4239. LUMCi022-B (115-2 and LUMC0115iATAX02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4240. LUMCi022-C (115-7 and LUMC0115iATAX07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4241. LUMCi023-A (LUMC0125iCTRL06 and 125-6)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4242. LUMCi023-A-1 (CQ_SCA1_1_26-37 and Qx8.5A.109.17.11 (37 repeats))

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4243. LUMCi023-A-2 (Qx8.5A.187.28.19 (42 repeats) and CQ_SCA1_1_26-42)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4244. LUMCi023-A-3 (Qx8.1.15.30.8 (54 repeats) and CQ_SCA1_1_29-54)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4245. LUMCi023-A-4 (Qx8.5A.178.5.34 (42 and 48 repeats) and CQ_SCA1_1_42-48)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4246. LUMCi027-A (LUMC0153iPKP03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Arrhythmogenic right ventricular dysplasia 9

  4247. LUMCi027-A-1 (iso01LUMC0153iPKP03 and LUMC0153iPKP03corr#22)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Arrhythmogenic right ventricular dysplasia 9

  4248. LUMCi028-A (LUMC0020iCTRL06 and FLB6)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4249. LUMCi029-A (LUMC0072iCTRL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4250. LUMCi029-A-2 (IsoLUMC0072iENG p.Met1Val-F5)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 1

  4251. LUMCi029-A-3 (IsoLUMC0072iALK1Het(p.Gly48Glu))

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4252. LUMCi029-B (LUMC0004iCTRL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4253. LUMCi030-A (LUMC0110iALK04)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Hereditary hemorrhagic telangiectasia

  4254. LUMCi030-A-1 (iso03LUMC0110iALK04)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Hereditary hemorrhagic telangiectasia

  4255. LUMCi030-B (LUMC0110iALK10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Hereditary hemorrhagic telangiectasia

  4256. LUMCi030-B-1 (iso01LUMC0110iALK10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Hereditary hemorrhagic telangiectasia

  4257. LUMCi031-A (LUMC0065iCTRL08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4258. LUMCi039-A (LQT1-1781G/A hiPSC and LUMC0021iKCNQ-30)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Long qt syndrome 1

  4259. LUMCi040-A (LUMC0053iSCN01B)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Brugada syndrome

  4260. LUMCi045-A (LUMC0145iKLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4261. LUMCi045-A-1 (iso01LUMC0145iKLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4262. LUMCi046-A (LUMC0146iKLHL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4263. LUMCi046-A-1 (iso2LUMC0146iKLHL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4264. LUMCi048-A (LUMCi048CTRL-A, 48CTRL-A and 48CTRL-3)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4265. LUMCi048-B (48CTRL-B, LUMCi048CTRL-B and 48CTRL-6)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4266. LUMCi048-C (LUMCi048CTRL-C, 48CTRL-C and 48CTRL-8)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4267. LUMCi049-A (LUMCi049SCA3-A, 49SCA3-A and 49SCA3-1)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4268. LUMCi049-B (LUMCi049SCA3-B, 49SCA3-B and 49SCA3-2)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4269. LUMCi049-C (LUMCi049SCA3-C, 49SCA3-C and 49SCA3-4)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4270. LUMCi051-A

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 7

  4271. LUMCi051-B

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 7

  4272. LUMCi052-A

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia 7

  4273. LUMCi052-B

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia 7

  4274. LUMCi052-C

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia 7

  4275. LUMCi054-A (CRB1 patient c.3122T>C p.(Met1041Thr) homozygote and LUMC0116iCRB09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  4276. LUMCi054-A-1 (LUMC0116iCRB09 ISO-02, LUMC0116iCRB09 homozygote CRISPR corrected isogenic clone 02 and iso02LUMC0116iCRB09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  4277. LUMCi054-A-2 (LUMC0116iCRB09 ISO-03, LUMC0116iCRB09 heterozygote CRISPR corrected isogenic clone 03 and iso03LUMC0116iCRB09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  4278. LUMCi055-A (CRB1 patient 117 compound heterozygous 2983G>T p.(Glu995*) c.1892A>G, p.(Tyr631Cys) and LUMC0117iCRB01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  4279. LUMCi056-A (CRB1 patient 128 compound heterozygous c.2843G>A p.(Cys948Tyr) and c.3122T>C p.(Met1041Thr) and LUMC0128iCRB01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  4280. LUMCi056-A-1 (LUMC0128iCRB01 heterozygote CRISPR corrected isogenic clone 02 and iso02LUMC0128iCRB01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  4281. LUMCi058-A (LUMCi231KLHL03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4282. LUMCi058-A-1 (Iso35LUMCi231KLHL03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4283. LUMCi059-A (LUMCi232KLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4284. LUMCi059-A-1 (Iso71LUMCi232KLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4285. LUMCi062-A (LUMC0322iFOPA-03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Single ventricle defect

    Disease:

    Congenital abnormality

  4286. LUMCi062-A-1 (iso1LUMC0322iFOPA-03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Single ventricle defect

    Disease:

    Congenital abnormality

  4287. LUMCi062-A-2 (iso2LUMC0322iFOPA-03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Single ventricle defect

    Disease:

    Congenital abnormality

  4288. LUMCi062-B (LUMC0322iFOPA-05)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Single ventricle defect

    Disease:

    Congenital abnormality

  4289. LUMCi062-C (LUMC0322iFOPA-06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Single ventricle defect

    Disease:

    Congenital abnormality

  4290. LUMCi063-A (LUMC0214iAPOL)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Chronic kidney disease

  4291. LUMCi064-A (LUMC0216iAPOL)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Chronic kidney disease

  4292. LUMCi064-A-1 (ISO1LUMC0216iAPOL05)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Chronic kidney disease

  4293. LUMCi064-A-2 (ISO3LUMC0216iAPOL05)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Chronic kidney disease

  4294. LUMCi065-A (LUMC0201iCSC02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Central serous chorioretinopathy

  4295. LUMCi067-A (LUMC0202iCSC01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Central serous chorioretinopathy

  4296. LUMCi068-A (LUMC0240iCSC02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Central serous chorioretinopathy

  4297. LUMCi069-A (LUMC0238iCSC06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Central serous chorioretinopathy

  4298. LUMCi070-A (APPV742L Clone B1)

    Netherlands Leiden University Medical Center (LUMC)

  4299. LUMCi070-B (APPV742L Clone D1)

    Netherlands Leiden University Medical Center (LUMC)

  4300. LUMCi070-C (APPV742L Clone K)

    Netherlands Leiden University Medical Center (LUMC)

  4301. LUMCi070-D (APPV742L Clone G)

    Netherlands Leiden University Medical Center (LUMC)

  4302. LVPEIi001-A (hiPSC-F2-3F1, LVIP01-NC-F2-1 and F2-4F)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Normal (average)

  4303. LVPEIi001-B (LVIP02-NC-F2-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Normal (average)

  4304. LVPEIi002-A (LVIP02-RB-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Retinoblastoma

  4305. RUCDRi002-A-63 (LVIP05-RB1-CS1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Retinoblastoma

  4306. RUCDRi002-A-64 (LVIP05-RB1-CS2)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Retinoblastoma

  4307. RUCDRi002-A-65 (LVIP05-RB1-CS3)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Retinoblastoma

  4308. LVPEIi004-A (LVIP02-LC2-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Leber congenital amaurosis 2

  4309. LVPEIi005-A (LVIP02-LC2-2)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Leber congenital amaurosis 2

  4310. LVPEIi006-A (LVIP02-LC12-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Leber congenital amaurosis 12

  4311. LVPEIi006-B (LVIP04-LC12-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Leber congenital amaurosis 12

  4312. LVPEIi006-B-1 (LVIP04-LC12-1-BE1 and VS-CTS-RD3-BE1, Clone 27)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Leber congenital amaurosis 12

  4313. LVPEIi007-B (LVIP04-SD1-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Stargardt disease

  4314. LVPEIi008-A (LVIP02-SD1-2)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Stargardt disease

  4315. LVPEIi008-B (LVIP04-SD1-2)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Stargardt disease

  4316. LZUSHi001-A (ips98)

    China Lanzhou University Second Hospital (LZUSH)
    Disease:

    Generalized epilepsy

  4317. LZUSHi002-A

    China Lanzhou University Second Hospital (LZUSH)
    Disease:

    Madd

  4318. LZUSHi003-A (DMD-27-delG)

    China Lanzhou University Second Hospital (LZUSH)
    Disease:

    Duchenne muscular dystrophy

  4319. MCRIi001-A (PB001)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4320. MCRIi001-A-1 (PB001-OI26)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Osteogenesis imperfecta

  4321. MCRIi001-A-2 (MCRIi001-A-SOX9tdTom and PB001-SOX9tdTom)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4322. UCSFi001-A-1M (iN-SRCAP-R2444-3)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Floating-harbor syndrome

  4323. UCSFi001-A-1N (iN-SRCAP-R2444-5)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Floating-harbor syndrome

  4324. MCRIi002-A (PB002)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4325. MCRIi003-A (PB003)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4326. MCRIi004-A (PB004)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4327. MCRIi005-A (PB005)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4328. MCRIi006-A (PB006)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4329. MCRIi007-A (PB007)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4330. MCRIi008-A (PB008)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4331. MCRIi009-A (PB009)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4332. MCRIi010-A (PB010)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4333. MCRIi019-A (1502)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4334. MCRIi025-A (CANVAS1-2)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4335. MCRIi025-B (CANVAS1-2 Het GC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4336. MCRIi026-A (CANVAS3-2)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4337. MCRIi026-B (CANVAS3-2 Het GC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4338. MCRIi027-A (CANVAS4-6)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4339. MCRIi027-B (CANVAS4-6 Het GC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4340. MCRIi029-A (808 iPSC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4341. MCRIi029-A-1 (GM21808-NAXEko-Cln19)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1

  4342. MCRIi029-A-2 (GM21808-NAXEko-Cln34)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1

  4343. MCRIi030-A (522 iPSC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4344. MCRIi031-A (468 iPSC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4345. MCRIi031-A-4 (GM03468-NAXEko-Cln2)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1

  4346. MCRIi031-A-5 (GM03468-NAXEko-Cln5)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1

  4347. MCRIi032-A (SCT 3010 iPSC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4348. MCRIi033-A (SCT 7002 iPSC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4349. MCRIi035-A (MCRIi-TC160154-UC-cl2)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4350. MCRIi035-B (MCRIi-TC160154-UC-cl5)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4351. MCRIi035-B-1 (MCRIi-TC160154-GC-cl5.1.49)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4352. MCRIi035-B-2 (MCRIi-TC160154-GC-cl5.30.4)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4353. MCRIi035-C (MCRIi-TC160154-UC-cl6)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4354. MCRIi036-A (MCRIi-TC110367-UC-cl4)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4355. MCRIi036-B (MCRIi-TC110367-UC-cl5)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4356. MCRIi036-B-1 (MCRIi-TC110367-GC-cl5.64.4.17)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4357. MCRIi036-C (MCRIi-TC110367-UC-cl6)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4358. MCRIi041-A (NF1_301_Cln9_UC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurofibromatosis type 1

  4359. MCRIi041-B (NF1_301_Cln8_GC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurofibromatosis type 1

  4360. MCRICBi002-B (GMP CB01 C3b)

    Australia Cord Blood Advanced Therapies Research Laboratory (MCRICB)
    Disease:

    Normal (average)

  4361. HMGUi001-A-22 (NCS1-KO Clone 19)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4362. MDCi007-A (8993-A12)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  4363. MDCi008-A (8993-B12)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  4364. MDCi009-A (8993-C11)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  4365. MDCi010-A (8993-D7)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  4366. MDCi011-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4367. MDCi011-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4368. MDCi012-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4369. MDCi012-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4370. MDCi013-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4371. MDCi013-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4372. MDCi014-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4373. MDCi014-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4374. WTSIi018-B-18 (Kolf 2.1 J (TARDBP M337V WT/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4375. WTSIi018-B-21 (Kolf 2.1 J (TARDBP M337V SNV/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4376. WTSIi018-B-22 (Kolf 2.1 J (TARDBP Q331K WT/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4377. WTSIi018-B-23 (Kolf 2.1 J (TARDBP Q331K SNV/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4378. WTSIi018-B-24 (Kolf 2.1 J (FUS R495X WT/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4379. WTSIi018-B-25 (Kolf 2.1 J (FUS R495X SNV/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4380. WTSIi018-B-26 (Kolf 2.1 J (FUS R521H WT/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4381. WTSIi018-B-27 (Kolf 2.1 J (FUS R521H SNV/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4382. MDCi233-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Limb-girdle muscular dystrophy type 2b

  4383. MDCi233-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Limb-girdle muscular dystrophy type 2b

  4384. MDCi237-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Maternally-inherited leigh syndrome

  4385. MDCi237-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Maternally-inherited leigh syndrome

  4386. MDCi238-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Maternally-inherited leigh syndrome

  4387. MDCi239-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Narp syndrome

  4388. METUi002-A

    Turkey Middle East Technical University (METU)

  4389. MHHi001-A (hHSC_Iso4_ADCF_SeViPS2 (Phönix))

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4390. MHHi001-A-6 (NRF2_A_Phönix-iPSC clone12)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4391. MHHi001-A-7 (NRF2_A_Phönix-iPSC clone19)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4392. MHHi001-A-20 (cyclinB1-eGFP hiPSCs)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4393. MHHi002-A (CF(1)iPS5)

    Germany Hannover Medical School (MHH)
    Disease:

    Cystic fibrosis

  4394. MHHi003-A (CF(15)iPS10)

    Germany Hannover Medical School (MHH)
    Disease:

    Cystic fibrosis

  4395. MHHi004-A (CF(16)iPS1)

    Germany Hannover Medical School (MHH)
    Disease:

    Cystic fibrosis

  4396. MHHi005-A (CF(17)iPS6)

    Germany Hannover Medical School (MHH)
    Disease:

    Cystic fibrosis

  4397. MHHi006-A (HSC1285_T-iPS2)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4398. MHHi015-A (hCD34iPSC16)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4399. MHHi015-B (hCD34iPSC11)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4400. MHHi029-A (F01 #20)

    Germany Hannover Medical School (MHH)

  4401. MHHi033-A (237_2020_01)

    Germany Hannover Medical School (MHH)
    Disease:

    Heritable pulmonary arterial hypertension

  4402. MHHi034-A (291_2020_01)

    Germany Hannover Medical School (MHH)
    Disease:

    Heritable pulmonary arterial hypertension

  4403. MHHi035-A (298_21_01)

    Germany Hannover Medical School (MHH)
    Disease:

    Heritable pulmonary arterial hypertension

  4404. MHHi036-A

    Germany Hannover Medical School (MHH)
    Disease:

    Heritable pulmonary arterial hypertension

  4405. MHHi037-A (207-21-01)

    Germany Hannover Medical School (MHH)
    Disease:

    Heritable pulmonary arterial hypertension

  4406. MHHi040-A (F10 #24)

    Germany Hannover Medical School (MHH)
    Disease:

    Fabry disease

  4407. MHHi041-A (F03 #3)

    Germany Hannover Medical School (MHH)
    Disease:

    Fabry disease

  4408. MHHi041-B (F03 #7)

    Germany Hannover Medical School (MHH)
    Disease:

    Fabry disease

  4409. MHHi042-A (F04 #13)

    Germany Hannover Medical School (MHH)
    Disease:

    Fabry disease

  4410. MHHi042-B (F04 #8)

    Germany Hannover Medical School (MHH)
    Disease:

    Fabry disease

  4411. MHHi043-A (F09 #26)

    Germany Hannover Medical School (MHH)
    Disease:

    Fabry disease

  4412. MHHi043-B (F09 #30)

    Germany Hannover Medical School (MHH)
    Disease:

    Fabry disease

  4413. MHRCCGi001-A (P1SH)

    Russia Laboratory Clinical Genetics (MHRCCG)
    Disease:

    Schizophrenia

  4414. MHRCCGi004-A (A1SH)

    Russia Laboratory Clinical Genetics (MHRCCG)
    Disease:

    Normal (average)

  4415. MHRCCGi005-A (A2SH)

    Russia Laboratory Clinical Genetics (MHRCCG)
    Disease:

    Normal (average)

  4416. MICCNi001-A (ADHD Stem Cell Study_subject 6, hiPSC_03 family control sibling and clone C1)

    Australia ​Monash Institute of Cognitive and Clinical Neurosciences (MICCN)
    Disease:

    Normal (average)

  4417. MICCNi001-B (ADHD Stem Cell Study_subject 6, hiPSC_03 family control sibling and clone C2)

    Australia ​Monash Institute of Cognitive and Clinical Neurosciences (MICCN)
    Disease:

    Normal (average)

  4418. MICCNi002-A (ADHD Stem Cell Study_subject 5, clone A1 and hiPSC_03 affected sibling)

    Australia ​Monash Institute of Cognitive and Clinical Neurosciences (MICCN)
    Disease:

    Obsolete_attention deficit hyperactivity disorder

  4419. MICCNi002-B (ADHD Stem Cell Study_subject 5, hiPSC_03 affected sibling and clone A16)

    Australia ​Monash Institute of Cognitive and Clinical Neurosciences (MICCN)
    Disease:

    Obsolete_attention deficit hyperactivity disorder

  4420. MILi001-A (K10 and hFF-iPSCs)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4421. MILi001-B (F5)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4422. MILi001-C (F10)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4423. MILi002-A (1E12 and CL220420-16632)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4424. MILi002-B (3E5 and CL220420-16634)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4425. MILi002-C (3D2 and CL220420-16630)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4426. MILi002-D (3D9 and CL220420-16631)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4427. MILi002-E (4D8 and CL220420-16633)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4428. MILi002-F (5C5 and CL220420-16635)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4429. MILi002-G (5E4 and CL220420-16636)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4430. MILi002-H (7C1 and CL220420-16637)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4431. MILi002-I (7C7 and CL220420-16639)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4432. MILi002-J (6G1 and CL220420-16638)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4433. MILi003-A (2H9 and CL220627-16697)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4434. MILi003-B (CL220627-16700 and 5A8)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4435. MILi003-C (CL220627-16699 and 4A2)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4436. MILi003-D (CL220627-16701 and 5C7)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4437. MILi003-E (CL220627-16698 and 3G2)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4438. MILi003-F (CL220627-16702 and 6F4)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4439. MILi004-A (1C3 and CL220725-16717)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4440. MILi004-B (CL220725-16720 and 3A3)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4441. MILi004-C (1C12 and CL220725-16716)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4442. MILi004-D (CL220725-16719 and 1H5)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4443. MILi004-E (CL220725-16721 and 3C9)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4444. MILi004-F (5B2 and CL220725-16722)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4445. MILi004-G (4E6 and CL220725-16724)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4446. MILi004-H (5E12 and CL220725-16723)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4447. MILi005-A (1E5 and CL230411-16867)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4448. MILi005-B (CL230411-16869 and 1D2)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4449. MILi005-C (2C3 and CL230411-16868)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4450. MILi005-D (5D3 and CL230411-16870)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4451. MILi005-E (6D2 and CL230411-16871)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4452. MILi006-A (4G9 and CL230530-16917)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4453. MIPTi001-A (NAA)

    Russia Moscow Institute of Physics and Technology (MIPT)
    Disease:

    X-linked adrenoleukodystrophy

  4454. MIPTi002-A

    Russia Moscow Institute of Physics and Technology (MIPT)
    Disease:

    Obsolete_hyperparathyroidism

  4455. MLi002-A (iEBS)

    Slovenia Faculty of Medicine University of Ljubljana (ML)
    Disease:

    Epidermolysis bullosa simplex

  4456. MLi002-A-1 (iso-hiEBS and hiEBS clone 8)

    Netherlands Faculty of Medicine University of Ljubljana (ML)
    Disease:

    Epidermolysis bullosa simplex

  4457. MLi003-A (iWT)

    United Kingdom Faculty of Medicine University of Ljubljana (ML)
    Disease:

    Normal (average)

  4458. MLi004-A (iMS)

    Slovenia Faculty of Medicine University of Ljubljana (ML)
    Disease:

    Epidermolysis bullosa dystrophica, autosomal recessive

  4459. MLi005-A (iDDEB)

    Slovenia Faculty of Medicine University of Ljubljana (ML)
    Disease:

    Epidermolysis bullosa dystrophica

  4460. MLUi001-M

    Germany Medical Faculty of the Martin Luther University Halle-Wittenberg (MLU)
    Disease:

    Schizophrenia

  4461. MLUi002-G

    Germany Medical Faculty of the Martin Luther University Halle-Wittenberg (MLU)
    Disease:

    Schizophrenia

  4462. MLUi007-J

    Germany Medical Faculty of the Martin Luther University Halle-Wittenberg (MLU)
    Disease:

    Alzheimer disease

  4463. MMCi001-A (MMC-iPSC-052B-02)

    Taiwan Mackay Medical College (MMC)
    Disease:

    Deafness, autosomal recessive 1a

  4464. MMCi002-A (MMC-iPSC-002-A)

    Taiwan Mackay Medical College (MMC)
    Disease:

    Hearing loss

  4465. MMGi001-A (EPI03-M-MB-D (T274M))

    France Marseille Medical Genetics Center - MMG (MMG)

  4466. MMGi002-A (12528-G (T287N))

    France Marseille Medical Genetics Center - MMG (MMG)

  4467. MMGi003-A (16312-TS (L203P))

    France Marseille Medical Genetics Center - MMG (MMG)

  4468. MNDi001-A (MND-Nek1-P001)

    Germany Institut für Anatomie und Zellbiologie, Universität Ulm (MND)
    Disease:

    Amyotrophic lateral sclerosis

  4469. MNDi002-A (MND-Nek1-P002)

    Germany Institut für Anatomie und Zellbiologie, Universität Ulm (MND)
    Disease:

    Amyotrophic lateral sclerosis

  4470. MNDi003-A (MND-Nek1-P003)

    Germany Institut für Anatomie und Zellbiologie, Universität Ulm (MND)
    Disease:

    Amyotrophic lateral sclerosis

  4471. MNDi004-A (MND-Nek1-P004)

    Germany Institut für Anatomie und Zellbiologie, Universität Ulm (MND)
    Disease:

    Amyotrophic lateral sclerosis

  4472. MNDi005-A (MND-Nek1/C9-P001)

    Germany Institut für Anatomie und Zellbiologie, Universität Ulm (MND)
    Disease:

    Amyotrophic lateral sclerosis

  4473. MNZTASi001-A (MS_0004, 2125-2 and TOB-02125)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Obsolete_primary progressive multiple sclerosis

  4474. MNZTASi002-A (MS_0001.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4475. MNZTASi003-A (MS_0002)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Obsolete_relapsing-remitting multiple sclerosis

  4476. MNZTASi004-A (MS_0003)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Obsolete_relapsing-remitting multiple sclerosis

  4477. MNZTASi005-A (MS_0006)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Obsolete_relapsing-remitting multiple sclerosis

  4478. MNZTASi006-A (MS_0005, TOB-02161 and 2161-4)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Obsolete_primary progressive multiple sclerosis

  4479. MNZTASi007-A (MS_0007)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Obsolete_relapsing-remitting multiple sclerosis

  4480. MNZTASi009-A (MS_0009.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4481. MNZTASi009-B (MS_0009.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4482. MNZTASi010-A (MS_0010)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4483. MNZTASi014-A (MS_0014)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4484. MNZTASi015-A (MS_0015.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4485. MNZTASi015-B (MS_0015.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4486. MNZTASi015-C (MS_0015.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4487. MNZTASi016-A (MS_0016)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4488. MNZTASi017-A (MS_0017)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4489. MNZTASi018-A (MS_0018)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4490. MNZTASi019-A (MS_0019)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4491. MNZTASi020-A (MS_0020.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4492. MNZTASi020-B (MS_0020.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4493. MNZTASi021-A (MS_0021)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4494. MNZTASi022-A (MS_0022)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4495. MNZTASi029-A (MS_0029.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4496. MNZTASi029-B (MS_0029.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4497. MNZTASi029-C (MS_0029.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4498. MNZTASi030-A (MS_0030.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4499. MNZTASi030-B (MS_0030.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4500. MNZTASi030-C (MS_0030.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4501. MNZTASi031-A (MS_0031.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Secondary progressive multiple sclerosis

  4502. MNZTASi031-B (MS_0031.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Secondary progressive multiple sclerosis

  4503. MNZTASi031-C (MS_0031.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Secondary progressive multiple sclerosis

  4504. MNZTASi032-A (MS_0032.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4505. MNZTASi032-B (MS_0032.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4506. MNZTASi032-C (MS_0032.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4507. MNZTASi033-A (MS_0033.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4508. MNZTASi033-B (MS_0033.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4509. MNZTASi033-C (MS_0033.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4510. MNZTASi034-A (MS_0034.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4511. MNZTASi034-B (MS_0034.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4512. MNZTASi034-C (MS_0034.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4513. MONUi001-A (86200001.1)

    Australia Monash University (MONU)
    Disease:

    Obsolete_autism spectrum disorder

  4514. MONUi001-B (86200001.2)

    Australia Monash University (MONU)
    Disease:

    Obsolete_autism spectrum disorder

  4515. MONUi001-C (86200001.4)

    Australia Monash University (MONU)
    Disease:

    Obsolete_autism spectrum disorder

  4516. MONUi002-A (86202443.3)

    Australia Monash University (MONU)
    Disease:

    Obsolete_autism spectrum disorder

  4517. MONUi002-B (86202443.5)

    Australia Monash University (MONU)
    Disease:

    Obsolete_autism spectrum disorder

  4518. MONUi002-C (86202443.6)

    Australia Monash University (MONU)
    Disease:

    Obsolete_autism spectrum disorder

  4519. MONUi003-A (86203213.1)

    Australia Monash University (MONU)
    Disease:

    Obsolete_autism spectrum disorder

  4520. MONUi003-B (86203213.2)

    Australia Monash University (MONU)
    Disease:

    Obsolete_autism spectrum disorder

  4521. MONUi003-C (86203213.4)

    Australia Monash University (MONU)
    Disease:

    Obsolete_autism spectrum disorder

  4522. MPIi001-A

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Normal (average)

  4523. MPIi002-A (T4 and L1-1Mut)

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Obsolete_parkinson's disease

  4524. MPIi003-A (IM2 and L2-2Mut)

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Obsolete_parkinson's disease

  4525. MPIi003-A-1 (IM2GC and L2-2GC)

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Obsolete_parkinson's disease

  4526. MPIi005-A (SF2.1 and wt1)

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Normal (average)

  4527. MPIPi057-A (UL1)

    Germany Max Planck Institute of Psychiatry (MPIP)
    Disease:

    Progressive myoclonic epilepsy type 1

  4528. MPIPi058-A (UL4)

    Germany Max Planck Institute of Psychiatry (MPIP)
    Disease:

    Progressive myoclonic epilepsy type 1

  4529. MRIi001-A (C6)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4530. MRIi001-A-1 (C6-AAVS1-iCasRx)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4531. MRIi003-A (HK)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4532. MRIi003-A-1 (MYH10+/-)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4533. MRIi003-A-2 (MYH10-/-)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4534. MRIi003-A-3 (TRPM4+/-)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4535. MRIi003-A-4 (TRPM4-/-)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4536. MRIi003-A-5 (AAVS1-CAG-VSFP-hetero)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4537. MRIi003-A-6 (AAVS1-CAG-VSFP-homo)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4538. MRIi003-A-7 (HK-AAVS1-iCasRx)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4539. MRIi003-A-8 (HK-AAVS1-CAG-eGFP-homo)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4540. MRIi003-A-9 (HK-AAVS1-CAG-FRT-stop-FRT-mKate2-hetero)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4541. MRIi003-A-10 (AAVS-CAG-DTPA-R heterozygous)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4542. MRIi003-A-11 (AAVS-CAG-DTPA-R homozygous)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4543. MRIi005-A

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Long qt syndrome 1

  4544. MRIi010-A (DCM)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Dilated cardiomyopathy 1g

  4545. MRIi016-A (Shox2.1)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Atrial fibrillation

  4546. MRIi017-A (TRPM4)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Brugada syndrome

  4547. MRIi018-A (HLHS_375)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Hypoplastic left heart syndrome

  4548. MRIi024-A (Shox2.2)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Atrial fibrillation

  4549. MRIi025-A (Noonan 3a)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Noonan syndrome

  4550. MRIi026-A (Noonan 3d)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Noonan syndrome

  4551. MRIi027-A (DMD 01)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Duchenne muscular dystrophy

  4552. MRIi028-A (PPC-4)

    Germany Klinikum rechts der Isar (MRI)

  4553. MRIi030-A (LVNC1)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Left ventricular noncompaction cardiomyopathy

  4554. MRIi031-A (LVNC2)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Left ventricular noncompaction cardiomyopathy

  4555. MRIi032-A (LVNC3)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Left ventricular noncompaction cardiomyopathy

  4556. MSKi002-A (C27 and iPS-27)

    United States Memorial Sloan Kettering Cancer Center (MSK)
    Disease:

    Normal (average)

  4557. MUi010-A (MYH9)

    Thailand Mahidol University (MU)
    Disease:

    Myh9-related syndromic thrombocytopenia

  4558. MUi015-A (RB1)

    Thailand Mahidol University (MU)
    Disease:

    Retinoblastoma

  4559. MUi026-A (MU012.C4)

    Thailand Mahidol University (MU)
    Disease:

    Obsolete_autosomal dominant polycystic kidney disease

  4560. MUi027-A (MU013.C2)

    Thailand Mahidol University (MU)

  4561. MUi028-A

    Thailand Mahidol University (MU)
    Disease:

    Normal (average)

  4562. MUi030-A (Gaucher iPSC2)

    Thailand Mahidol University (MU)
    Disease:

    Gaucher disease type 3

  4563. MUi031-A (Gaucher iPSC3)

    Thailand Mahidol University (MU)
    Disease:

    Gaucher disease type 3

  4564. MUi032-A

    Thailand Mahidol University (MU)
    Disease:

    Choroideremia

  4565. MUi033-A (MU020 and homoHbE iPSC)

    Thailand Mahidol University (MU)
    Disease:

    Normal (average)

  4566. MUi034-A (homoHbCS iPSC and MU018)

    Thailand Mahidol University (MU)
    Disease:

    Alpha thalassemia spectrum

  4567. MUi036-A

    Thailand Mahidol University (MU)
    Disease:

    Normal (average)

  4568. MUi038-A (EYS mutation)

    Thailand Mahidol University (MU)
    Disease:

    Retinitis pigmentosa

  4569. MUi040-A

    Thailand Mahidol University (MU)
    Disease:

    Amyloidosis

  4570. MUBi002-A (CF 001)

    Poland Medical University of Bialystok (MUB)
    Disease:

    Cystic fibrosis

  4571. MUBi005-A (iPSC_COPD)

    Poland Medical University of Bialystok (MUB)
    Disease:

    Chronic obstructive pulmonary disease

  4572. MULi001-A (iPSC-RESET-#21)

    Poland Medical University of Lodz (MUL)
    Disease:

    Thrombocytopenia 5

  4573. MUNIi001-A (DMD02)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  4574. MUNIi002-A (MDMD02)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  4575. MUNIi003-A (DMD03)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  4576. MUNIi004-A (DMD04)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  4577. MUNIi005-A (fAD1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer disease 3

  4578. MUNIi006-A (fAD2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer disease 3

  4579. MUNIi007-A (fAD3 and ADF81)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer disease 4

  4580. MUNIi008-A (fWT1, WTM52, fHC1 and fCTRL1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4581. MUNIi009-A (fWT2, WTF50, fHC2 and fCTRL2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4582. MUNIi010-A (WTF80, fHC3, fWT3 and fCTRL3)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4583. MUNIi011-A (BAD1 and sAD1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer's disease

  4584. MUNIi012-A (BAD2 and sAD2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer's disease

  4585. MUNIi013-A (BAD4 and sAD3)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer's disease

  4586. MUNIi014-A (sHC1, BHC2 and sCTRL1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4587. MUNIi015-A (sHC2, BHC1 and sCTRL2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4588. MUNIi016-A (sHC3, BHC3 and sCTRL3)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4589. MUNIi017-A (BWT3)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4590. MUNIi018-A (HUVEC-iPSC)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4591. MUNIi018-B (HUVEC-hiPSC-macroH2A1.1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4592. MUNIi018-C (HUVEC-hiPSC-macroH2A1.2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4593. MUNIi018-D (mHU-C)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4594. MUNIi019-A (NBS-M and NBS)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Nijmegen breakage syndrome

  4595. MUNIi020-A (sHC5)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4596. MUNIi021-A (sAD5)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer's disease

  4597. MUNIi022-A (PKP2 and PKP2_AKAP9)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  4598. MUNIi023-A (mUC-K)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4599. MUNIi024-A (PB2C1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4600. MUNIi025-A (mLAM-A)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4601. MUNIi025-B (mLAM-D)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4602. MURAi001-A (TET1mutationC18)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)

  4603. MURAi002-A (-4bp/HbE C11)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Hemoglobin e-beta-thalassemia syndrome

  4604. MURAi003-A (HoHLA, Homozygous-HLA and HoHLA C3)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Normal (average)

  4605. MURAi004-A (Bart)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Junctional epidermolysis bullosa

  4606. MURAi006-A (FL23C9)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Hemoglobin e-beta-thalassemia syndrome

  4607. MURAi007-A

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Inherited retinal dystrophy

  4608. MURAi009-A

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Normal (average)

  4609. MUSCSDi001-A (iPSK3)

    United States Steve's Duncan Lab (MUSCSD)
    Disease:

    Normal (average)

  4610. MUSCSDi001-A-1 (PCCB ∆14/∆29)

    United States Steve's Duncan Lab (MUSCSD)
    Disease:

    Propionic acidemia

  4611. MUSCSDi001-A-2 (PCCB ∆19/∆481)

    United States Steve's Duncan Lab (MUSCSD)
    Disease:

    Propionic acidemia

  4612. MUSIi001-A (SFiPSC01)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4613. MUSIi001-A-1 (B2M-KO-SFiPSC5 and HLA-I-null SFiPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4614. MUSIi001-A-2 (HLA-I/II-null SFiPSCs and B2M-/-/CIITA-/- SFiPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4615. MUSIi001-A-3 (TIGIT-KO-SFiPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4616. MUSIi004-A

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Spinocerebellar ataxia type 3

  4617. MUSIi005-A (SUiPSC02)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4618. MUSIi006-A (SKiPSC02)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4619. MUSIi009-A (HDF-iPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4620. MUSIi011-A (STiPSC01.1)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4621. MUSIi011-B (STiPSC01.8)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4622. MUSIi013-A (CBNK-iPSC)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4623. MUSIi013-A-2 (CAR-TIM3 iPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4624. MUSIi016-A (TyO)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4625. MUSIi017-A (Oneg)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4626. MUSIi019-A (SLC4A1-21-C1)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Distal renal tubular acidosis

  4627. MUSIi023-A (hmziPSC and Homozygous HLA iPSC)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4628. NCAi001-A

    Netherlands Ncardia B.V. (NCA)
    Disease:

    Normal (average)

  4629. NCBSi003-A (Park14-R741Q-2022)

    India National Center for Biological Sciences (NCBS)
    Disease:

    Autosomal recessive parkinson disease 14

  4630. NCBSi004-A (Park14-control-2022)

    India National Center for Biological Sciences (NCBS)
    Disease:

    Normal (average)

  4631. NCCSEDi001-A

    China National Chengdu Center for Safety Evaluation of Drugs (NCCSED)
    Disease:

    Normal (average)

  4632. NCCSEDi001-A-1

    China National Chengdu Center for Safety Evaluation of Drugs (NCCSED)
    Disease:

    Intellectual developmental disorder 61

  4633. NCHi001-A (LCL-iPSC4802)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Congenital heart disease

  4634. NCHi003-A (NCH005)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Pulmonary valve atresia with intact ventricular septum

  4635. NCHi004-A (NCH140)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Down syndrome

  4636. NCHi006-A (NCH023)

    United States Nationwide Children's Hospital (NCH)

  4637. NCHi009-A (NCH78)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Hypoplastic left heart syndrome

  4638. NCHi010-A (NCH141)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Down syndrome

  4639. NCHi011-A (NCH092)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Alagille syndrome

  4640. NCHi012-A (NCH089)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Alagille syndrome

  4641. NCHi013-A (NCH17)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Pulmonary valve atresia with intact ventricular septum

  4642. NCHi014-A (NCH3-N1HET)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Normal (average)

  4643. NCHi015-A (NCH178)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Type i truncus arteriosus

  4644. NCHi016-A (NCH012)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Pulmonary atresia-intact ventricular septum syndrome

  4645. NCHi020-A (S63del hiPSCs)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Charcot-marie-tooth disease type 1b

  4646. NCHi021-A (R98C hiPSCs)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Charcot-marie-tooth disease type 1b

  4647. NCHi023-A (NCH217)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Nemaline myopathy

  4648. NCHi024-A (NCH27)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Bicuspid aortic valve

  4649. NCHi025-A

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Pulmonary stenosis

  4650. NCHi026-A (iPSC486AB)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Duchenne muscular dystrophy

  4651. NCHi027-A

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Cloaca

  4652. NCHi028-A

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Prune belly syndrome

  4653. NCHi030-A (NCH80)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Normal (average)

  4654. NCKDi006-A (NCKD-iPS-FSGS-TRPC6-006)

    China National Center of Kidney Diseases (NCKD)
    Disease:

    Focal segmental glomerulosclerosis

  4655. NCKUi001-A (human amniotic fluid stem cells derived iPSC and hAFSC-iPSC)

    Taiwan National Cheng Kung University (NCKU)
    Disease:

    Normal (average)

  4656. NCSi001-A (NCS065)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Alzheimer's disease

  4657. NCSi002-A (NCS066)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Normal (average)

  4658. NCSi003-A (NCS067)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Normal (average)

  4659. NCSi004-A (NCS068)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Normal (average)

  4660. NCSi005-A (NCS069)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Alzheimer's disease

  4661. NCSi006-A (NCS070)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Normal (average)

  4662. NCSi007-A (NCS071)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Alzheimer's disease

  4663. NEIi001-A (iPSC-F34)

    United States National institutes of Health (NEI)
    Disease:

    Opa1-related optic atrophy with or without extraocular features

  4664. NEIi002-A (iPSC-F35)

    United States National institutes of Health (NEI)
    Disease:

    Opa1-related optic atrophy with or without extraocular features

  4665. NEIi003-A (iPSC-F36)

    United States National institutes of Health (NEI)
    Disease:

    Opa1-related optic atrophy with or without extraocular features

  4666. NEIi004-A (iPSC-F41)

    United States National institutes of Health (NEI)
    Disease:

    Opa1-related optic atrophy with or without extraocular features

  4667. NENCKIi001-A (MPAN-3.1)

    Poland Nencki Institute of Experimental Biology PAS (NENCKI)
    Disease:

    Mitochondrial membrane protein-associated neurodegeneration

  4668. NENCKIi002-A (MPAN-9.3)

    Poland Nencki Institute of Experimental Biology PAS (NENCKI)
    Disease:

    Mitochondrial membrane protein-associated neurodegeneration

  4669. NENCKIi003-A (MPAN-18.1)

    Poland Nencki Institute of Experimental Biology PAS (NENCKI)
    Disease:

    Mitochondrial membrane protein-associated neurodegeneration

  4670. NENCKIi004-A (MPAN-22.3)

    Poland Nencki Institute of Experimental Biology PAS (NENCKI)
    Disease:

    Mitochondrial membrane protein-associated neurodegeneration

  4671. NERCi001-A

    China National Engineering and Research Center of Human Stem Cell (NERC)
    Disease:

    Dyskeratosis congenita

  4672. NFHHMUi001-A

    China Department of Neurosurgery of The First Affiliated Hospital of Harbin Medical University (NFHHMU)
    Disease:

    Cerebral cavernous malformation

  4673. NHGRIi001-A (iPSC-1 and FISAL04_Sia80)

    United States National Human Genome Research Institute (NHGRI)

  4674. NHGRIi002-A (iPSC-2 and CDG.1121_Sia74)

    United States National Human Genome Research Institute (NHGRI)

  4675. NHLBIi001-A (MS19-ES-D)

    United States NHLBI iPSC Core (NHLBI)
    Disease:

    Normal (average)

  4676. NHLBIi001-B (MS19-ES-H)

    United States NHLBI iPSC Core (NHLBI)
    Disease:

    Normal (average)

  4677. NHLBIi003-A (ND2.0 and mND2-0)

    United States NHLBI iPSC Core (NHLBI)
    Disease:

    Normal (average)

  4678. NHLBIi003-A-1 (ND2-tdTom1)

    United States NHLBI iPSC Core (NHLBI)
    Disease:

    Normal (average)

  4679. NHLBIi003-A-2 (ND2-tdTom4)

    United States NHLBI iPSC Core (NHLBI)
    Disease:

    Normal (average)

  4680. NIHTVBi016-A (HT876D)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  4681. NIHTVBi017-A (HT939A)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  4682. NIHTVBi018-A (HT940B)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  4683. NIHTVBi019-A (HT852)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Leukodystrophy

  4684. NIHTVBi019-A-1 (HT852-DC)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Leukodystrophy

  4685. NIHTVBi020-A (HT853)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Normal (average)

  4686. NIHTVBi021-A (HT854)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Normal (average)

  4687. NIHTVBi022-A (HT964)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Leukodystrophy

  4688. NIHTVBi024-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  4689. NIHTVBi025-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Sting-associated vasculopathy with onset in infancy

  4690. NIHTVBi026-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Sting-associated vasculopathy with onset in infancy

  4691. NIHTVBi027-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Sting-associated vasculopathy with onset in infancy

  4692. NIHTVBi028-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Lyn gene mutation

  4693. NIHTVBi029-A (HT1127A (NIHTVBi029-A))

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Cdc42

  4694. NIHTVBi030-A (HT1128A (NIHTVBi030-A))

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Cdc42 gene

  4695. NIHTVBi031-A (HT1129D)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Autoimmune interstitial lung, joint, and kidney disease

  4696. NIMHi001-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Obsolete_parkinson's disease

  4697. NIMHi001-A-1 (PD01 Isogenic)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Obsolete_parkinson's disease

  4698. NIMHi002-A (BPPD02)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Parkinson disease

  4699. NIMHi003-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Parkinson disease

  4700. NIMHi004-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4701. NIMHi005-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4702. NIMHi006-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4703. NIMHi007-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4704. NIMHi008-A (NphyiALS1)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Amyotrophic lateral sclerosis

  4705. NIMHi009-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4706. NIMHi010-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4707. NIMHi011-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Congenital myasthenic syndrome

  4708. NIMHi012-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Epilepsy

  4709. NIMHi013-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Epilepsy

  4710. NIMHi014-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Epilepsy

  4711. NIMHi015-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Autosomal recessive juvenile parkinson disease 2

  4712. NIMHi016-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Phosphoglycerate kinase 1 deficiency

  4713. NIMHi017-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Biotin-responsive basal ganglia disease

  4714. NIMHi018-A (PD07)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Parkinson's disease 6

  4715. NIMHi019-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Congenital myasthenic syndrome

  4716. NIMHi020-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Mitochondrial disease

  4717. NIMHi021-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4718. NIMHi022-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Congenital myasthenic syndrome

  4719. NIMHi023-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4720. NIMHi026-A (MSA1)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Multiple system atrophy

  4721. NIMHi027-A (PD09)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Early-onset parkinson's disease

  4722. NIMHi028-A (MSA04)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Multiple system atrophy

  4723. NIMHi032-A (PSP03)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Progressive supranuclear palsy

  4724. NIMHi033-A (CBMNIMH_G381)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Autism spectrum disorder

  4725. NIMHi034-A (NphyiNC2)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4726. NJDTHi001-A

    China Department of Cardio-Thoracic Surgery, Nanjing Drum Tower Hospital (NJDTH)
    Disease:

    Danon disease

  4727. NMIi001-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Normal (average)

  4728. TMOi001-A-5 (DISC1 Ex2 D5)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Normal (average)

  4729. TMOi001-A-6 (DISC1 Ex2 C4)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Normal (average)

  4730. NMIi002-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4731. NMIi002-B

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4732. NMIi004-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4733. NMIi005-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4734. NMIi006-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4735. NMIi006-B

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4736. NMIi010-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Normal (average)

  4737. NMIi011-A (B1.4)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4738. NMIi011-B (B1.6)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4739. NMIi011-C (B1.7)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4740. NMIi011-D (B1.10)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4741. NMIi012-A (DG1)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4742. NMIi012-B (DG2)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4743. NMIi012-D (DG4)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4744. NMIi012-E (DG5)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4745. NRIFPi001-A (WJWKYSi001-A)

    China National Research Institute for Family Planning (NRIFP)
    Disease:

    Phenylketonuria

  4746. NSi003-A (NSi-DS)

    India Stem Cell and Neurobiology Lab (NS)
    Disease:

    Down syndrome

  4747. NSi003-B (NSi-isoEu)

    India Stem Cell and Neurobiology Lab (NS)
    Disease:

    Down syndrome

  4748. NSHDMUi001-A

    China Department of Neurology of the Second Hospital of Dalian Medical University (NSHDMU)
    Disease:

    Obsolete_diabetes mellitus

  4749. NTUHi002-A

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Aceruloplasminemia

  4750. NTUHi003-A (NTUH-iPSC-003-40)

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Premature ovarian insufficiency

  4751. NTUHi004-A

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Leigh syndrome

  4752. NTUHi005-A (IBMS-iPSC-071-01)

    Taiwan National Taiwan University Hospital (NTUH)

  4753. NTUHi006-A (NTUH-iPSC-008-1)

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Polycystic ovary syndrome

  4754. NTUHi007-A (IBMS-iPSC-104-02)

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Parkinson disease

  4755. NUIGi001-A (iPSC ARO1-11)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autosomal recessive osteopetrosis

  4756. NUIGi003-A (LQT002C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4757. NUIGi003-B (LQT002C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4758. NUIGi004-A (LQT003C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4759. NUIGi005-A (LQTS004C7 and LQT004C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4760. NUIGi005-B (LQTS004C9 and LQT004C9)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4761. NUIGi005-C (LQTS004Cx and LQT004Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4762. NUIGi006-A (LQTS005C2 and LQT005C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4763. NUIGi006-B (LQTS005C4 and LQT005C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4764. NUIGi006-C (LQTS005Cx and LQT005Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4765. NUIGi007-A (LQTS006C6 and LQT006C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4766. NUIGi007-B (LQTS006C8 and LQT006C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4767. NUIGi008-A (LQTS007C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4768. NUIGi008-B (LQTS007C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4769. NUIGi008-C (LQTS007Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4770. NUIGi009-A (LQTS008C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4771. NUIGi009-B (LQTS008C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4772. NUIGi009-C (LQTS008Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4773. NUIGi010-A (LQTS009C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4774. NUIGi010-B (LQTS009C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4775. NUIGi010-C (LQTS009Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4776. NUIGi011-A (LQTS010C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4777. NUIGi011-B (LQTS010C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4778. NUIGi011-C (LQTS010Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4779. NUIGi012-A (LQT011C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4780. NUIGi015-A (LQT014C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4781. NUIGi015-B (LQT014C9)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4782. NUIGi015-C (LQT014C12)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4783. NUIGi018-A (LQT017C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4784. NUIGi018-B (LQT017C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4785. NUIGi018-C (LQT017Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4786. NUIGi020-A (LQT019C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4787. NUIGi020-B (LQT019C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4788. NUIGi020-C (LQT019Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4789. NUIGi022-A (ND11C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4790. NUIGi022-B (ND11C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4791. NUIGi023-A (ND12C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4792. NUIGi023-B (ND12C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4793. NUIGi024-A (CND13C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4794. NUIGi024-B (CND13C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4795. NUIGi025-A (ND14C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4796. NUIGi025-B (ND14C9)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4797. NUIGi026-A (CND15C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4798. NUIGi026-B (CND15C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4799. NUIGi027-A (RP001C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Retinitis pigmentosa

  4800. NUIGi028-A (RP002C12)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Retinitis pigmentosa

  4801. NUIGi029-A (RP003C12)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Retinitis pigmentosa

  4802. NUIGi033-A (ASD012-Q)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism spectrum disorder

  4803. NUIGi034-A (ASDC012-AI)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4804. NUIGi035-A (02V-AD)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4805. NUIGi036-A (03V-D)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4806. NUIGi037-A (05C-J)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4807. NUIGi038-A (LQTH002C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4808. NUIGi038-B (LQTH002Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4809. NUIGi038-B-1 (CR.LQTH002Cx-A17)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4810. NUIGi038-B-2 (CR.LQTH002Cx-A21)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4811. NUIGi038-B-3 (CR.LQTH002Cx-3A15)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4812. NUIGi038-B-4 (CR.LQTH002Cx-3A18)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4813. NUIGi038-C (LQTH002C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4814. NUIGi039-A (ND1C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_autism spectrum disorder

  4815. NUIGi039-B (ND1C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_autism spectrum disorder

  4816. NUIGi040-A (CND1C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4817. NUIGi040-B (CND1C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4818. NUIGi041-A (ND3C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_autism spectrum disorder

  4819. NUIGi041-B (ND3C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_autism spectrum disorder

  4820. NUIGi042-A (CND3C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4821. NUIGi042-B (CND3C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4822. NUIGi043-A (ALS52C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4823. NUIGi043-B (ALS52C9)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4824. NUIGi043-C (ALS52C10)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4825. NUIGi044-A (ALS69C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4826. NUIGi044-B (ALS69C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4827. NUIGi044-C (ALS69C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4828. NUIGi045-A (ND2C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_autism spectrum disorder

  4829. NUIGi046-A (LQTH001C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4830. NUIGi046-B (LQTH001C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4831. NUIGi046-C (LQTH001C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4832. NUIGi047-A (LQTH003C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4833. NUIGi047-B (LQTH003C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4834. NUIGi047-C (LQTH003Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4835. NUIGi048-A (ALSH84C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4836. NUIGi048-B (ALSH84C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4837. NUIGi048-C (ALSH84C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4838. NUIGi049-A (ALSH47C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4839. NUIGi049-B (ALSH47C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4840. NUIGi049-C (ALSH47C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4841. NUIGi050-A (ALS53C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4842. NUIGi050-B (ALS53C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4843. NUIGi050-C (ALS53C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4844. NUIGi051-A (ALS57C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4845. NUIGi051-B (ALS57C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4846. NUIGi051-C (ALS57C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4847. NUIGi052-A

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Non-specific early-onset epileptic encephalopathy

  4848. NUIGi052-B

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Non-specific early-onset epileptic encephalopathy

  4849. NUIGi052-C

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Non-specific early-onset epileptic encephalopathy

  4850. NUIGi055-A (iPSC C1-15)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4851. NUIGi055-B (iPSC C1-16)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4852. NUIGi055-C (iPSC C1-17)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4853. NUIGi057-A (EP2004 C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Developmental and epileptic encephalopathy

  4854. NUIGi057-B (EP2004 C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Developmental and epileptic encephalopathy

  4855. NUIGi057-C (EP2004 C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Developmental and epileptic encephalopathy

  4856. NUIGi058-A (EP2C004 C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4857. NUIGi058-B (EP2C004 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4858. NUIGi058-C (EP2C004 C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4859. NUIGi059-A (EP2001 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Epileptic encephalopathy

  4860. NUIGi059-B (EP2001 C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Epileptic encephalopathy

  4861. NUIGi059-C (EP2001 C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Epileptic encephalopathy

  4862. NUIGi060-A (EP2C001 C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4863. NUIGi060-B (EP2C001 C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4864. NUIGi060-C (EP2C001 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4865. NUIGi061-A (EP2002 C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Developmental and epileptic encephalopathy

  4866. NUIGi061-B (EP2002 C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Developmental and epileptic encephalopathy

  4867. NUIGi061-C (EP2002 C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Developmental and epileptic encephalopathy

  4868. NUIGi062-A (EP2C002 C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4869. NUIGi062-B (EP2C002 C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4870. NUIGi062-C (EP2C002 C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4871. NUIGi063-A (EP2003 C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Kcnq2-related developmental and epileptic encephalopathy

  4872. NUIGi063-B (EP2003 C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Kcnq2-related developmental and epileptic encephalopathy

  4873. NUIGi063-C (EP2003 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Kcnq2-related developmental and epileptic encephalopathy

  4874. NUIGi064-A (EP2C003 C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4875. NUIGi064-B (EP2C003 C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4876. NUIGi064-C (EP2C003 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4877. NUMNi001-A

    Japan Department of Nephrology, Nagoya University Hospital (NUMN)
    Disease:

    Normal (average)

  4878. NUMNi002-A

    Japan Department of Nephrology, Nagoya University Hospital (NUMN)

  4879. NUMNi003-A

    Japan Department of Nephrology, Nagoya University Hospital (NUMN)
    Disease:

    Autosomal dominant polycystic kidney disease

  4880. NYSCFi001-A (AL0002-01-MR-131)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4881. NYSCFi001-B (AL0002-01-MR-132)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4882. NYSCFi001-C (AL0002-01-SV-008)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4883. NYSCFi001-D (AL0002-01-SV-010)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4884. NYSCFi002-A (AL0004-01-SV-002)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4885. NYSCFi002-B (AL0004-01-SV-008)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4886. NYSCFi003-A (CO0002-01-SV-003)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Alzheimer's disease

  4887. NYSCFi008-A (BR0010-01-MSV-163)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Ogden syndrome

  4888. NYSCFi008-A-1 (BR0010-01-MCS-421-EDIT0062B)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Ogden syndrome

  4889. NYSCFi020-A (BR0015-01-MCS-224-EDIT0138)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Ogden syndrome

  4890. NYSCFi020-A-1

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Ogden syndrome

  4891. NYSCFi020-A-2 (BR0015-01-MCS-671-EDIT0138)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Ogden syndrome

  4892. OFi001-A (ASD011-A)

    South Korea OrganFactory (OF)
    Disease:

    Autism spectrum disorder

  4893. OFi002-A (OFi015-A)

    South Korea OrganFactory (OF)
    Disease:

    Autism spectrum disorder

  4894. OGIi001-A

    United States Ocular Genomics Institute at Mass Eye and Ear Hospital (OGI)
    Disease:

    Normal (average)

  4895. ORIONi001-A (iALS-1)

    Slovakia Biomedical center Martin, Jessenius Faculty of Medicine in Martin, COMENIUS UNIVERSITY IN BRATISLAVA (ORION)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4896. ORIONi002-A (iALS-2)

    Slovakia Biomedical center Martin, Jessenius Faculty of Medicine in Martin, COMENIUS UNIVERSITY IN BRATISLAVA (ORION)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  4897. ORIONi003-A

    Slovakia Biomedical center Martin, Jessenius Faculty of Medicine in Martin, COMENIUS UNIVERSITY IN BRATISLAVA (ORION)
    Disease:

    Duchenne muscular dystrophy

  4898. ORIONi004-A (iDMD-2)

    Slovakia Biomedical center Martin, Jessenius Faculty of Medicine in Martin, COMENIUS UNIVERSITY IN BRATISLAVA (ORION)
    Disease:

    Duchenne and becker muscular dystrophy

  4899. OSRi001-A (PD-OPA1-A495V#72)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Parkinson disease

  4900. OSRi004-A (ND#37)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Normal (average)

  4901. OSRi005-A (ND#68)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Normal (average)

  4902. OSRi009-A (SGS_D868N)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Schinzel-giedion midface-retraction syndrome

  4903. OSRi009-A-1 (SGS_D868D)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Schinzel-giedion midface-retraction syndrome

  4904. OSRi010-A (SGS_I871T)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Schinzel-giedion midface-retraction syndrome

  4905. OSRi010-A-1 (SGS_I871I)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Schinzel-giedion midface-retraction syndrome

  4906. OSRi011-A (4xSNCA)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Parkinsonian disorder

  4907. OSRi011-A-1 (Iso SNCA)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Parkinsonian disorder

  4908. OSRi013-A (OSR_001#10)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Multiple sclerosis

  4909. OSRi014-A (OSR_002#1)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Multiple sclerosis

  4910. OSRi015-A (OSR_003#56)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Multiple sclerosis

  4911. OSRi016-A (OSR_004#30)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Multiple sclerosis

  4912. OSRi017-A (PTL6)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4913. OSRi017-A-1 (PTL6-SD10)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4914. OSRi017-A-2 (PTL6-LD3)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4915. OSRi018-A (PTS36)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4916. OSRi018-A-1 (PTS36-SD23)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4917. OSRi018-A-2 (PTS36-LD3)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4918. OTATi001-A (HC4)

    United States Office of Tissues and Advanced Therapies, CBER, FDA (OTAT)
    Disease:

    Normal (average)

  4919. OTATi002-A (HC8)

    United States Office of Tissues and Advanced Therapies, CBER, FDA (OTAT)
    Disease:

    Normal (average)

  4920. PCIi001-A (PC124)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4921. PCIi003-A (PC126)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4922. PCIi004-A (PC127)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4923. PCIi005-A (PC137)

    France PHENOCELL (PCI)
    Disease:

    Danon disease

  4924. PCIi007-A (PC153)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4925. PCIi008-A (PC154)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4926. PCIi009-A (PC168)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4927. PCIi010-A (PC169)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4928. PCIi011-A (PC170)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4929. PCIi012-A (PC171)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4930. PCIi015-A (PC191)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4931. PCIi016-A (PC192)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4932. PCIi017-A (PC198)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4933. PCIi018-A (PC199)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4934. PCIi019-A (PC200)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4935. PCIi020-A (PC201)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4936. PCIi021-A (PC202)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4937. PCIi022-A (PC203)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4938. PCIi023-A (PC204)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4939. PCIi024-A (PC205)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4940. PCIi025-A (PC084)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  4941. PCIi026-A (PC085)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  4942. PCIi027-A (PC086)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  4943. PCIi029-A (PC076)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome type 1

  4944. PCIi030-A (PC078)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome type 1

  4945. PCIi031-A (PC079)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome type 1

  4946. PCIi032-A (PC087)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  4947. PCIi033-A (PCi-CAU2)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4948. PCIi034-A (PC138)

    France PHENOCELL (PCI)
    Disease:

    Aicardi-goutieres syndrome

  4949. PCIi035-A (PC139)

    France PHENOCELL (PCI)
    Disease:

    Aicardi-goutieres syndrome

  4950. WTSIi018-B-13

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Ataxia telangiectasia syndrome

  4951. WTSIi018-B-14

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Ataxia telangiectasia syndrome

  4952. WTSIi018-B-15

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Ataxia telangiectasia syndrome

  4953. WTSIi018-B-16

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Ataxia telangiectasia syndrome

  4954. PEIi021-A (PEIi004-A)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4955. PEIi021-B (PEIi004-B)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4956. PEIi021-C (PEIi004-C)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4957. PEIi021-D (PEIi004-D)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4958. PEIi022-A (PEIi005-A)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4959. PEIi022-B (PEIi005-B)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4960. PEIi022-C (PEIi005-C)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4961. PEIi022-D (PEIi005-D)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4962. PENNi001-A (PENN123i-SV20 and SV20)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4963. PENNi001-A-1 (SV20 ACE2KO D1)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4964. PENNi002-A (ND535 Sev1)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4965. PENNi003-A (HPAP021 Sev2)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  4966. PENNi004-A (HPAP030 Sev10)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  4967. PENNi005-A (HPAP031 Sev7)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  4968. PENNi006-A (HPAP112 Sev12)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4969. PENNi007-A (HPAP114 Sev10)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4970. PENNi008-A (HPAP135 Sev7)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  4971. PENNi009-A (HPAP149 Sev3)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  4972. PENNi010-A (HPAP155 Sev2)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4973. PFIZi001-A (EM1-3F)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4974. RCi001-A (Thp3C-6 and RCi88)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4975. RCi001-B (RCi89 and Thp3C-9)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4976. PFIZi002-A (EM1-7M)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4977. RCi002-A (FP5C-14 and RCi92)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4978. RCi002-B (FP5C-16 and RCi93)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4979. PFIZi003-A (EM2-7M)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4980. RCi003-A (RCi115 and CIP11A-5)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Obsolete_pain agnosia

  4981. RCi003-B (CIP11A-9 and RCi117)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Obsolete_pain agnosia

  4982. PFIZi004-A (EM2-7F)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4983. PFIZi009-A (RCi188)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4984. PFIZi010-A (FB65c7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  4985. PFIZi010-B (FB65c16)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  4986. PFIZi010-C (FB65c20)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  4987. PFIZi011-A (RCi199 and FB67c2)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  4988. PFIZi012-A (FB66c17 and RCi198)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  4989. PFIZi013-A (RCi215 and RCFB59 C9)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Amyotrophic lateral sclerosis

  4990. PFIZi014-A (OD002-s7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4991. PFIZi015-A (OD003-s5)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4992. PFIZi016-A (OD005-s9)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4993. PFIZi017-A (BC142c7 and RCi209)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4994. PFIZi018-A (BC143c8 and RCi207)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4995. PFIZi019-A (RCi202 and BC145c6)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4996. PFIZi021-A (OD001-s7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4997. PFIZi022-A (B219c2)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epileptic encephalopathy

  4998. PFIZi023-A (B217c8)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Bilateral frontoparietal polymicrogyria

  4999. PFIZi024-A (B218c6)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Obsolete_epilepsy

  5000. PFIZi025-A (B220c16)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Obsolete_epilepsy

  5001. PFIZi027-A (B221c13)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Lissencephaly

  5002. PFIZi028-A (B212c7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Neurodevelopmental disorder

  5003. PFIZi029-A (B222c4)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Obsolete_myoclonic epilepsy

  5004. PFIZi030-A (B216c13)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Acromesomelic dysplasia

  5005. PFIZi031-A (B213c1)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epileptic encephalopathy

  5006. PFIZi032-A (B214c8)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Tuberous sclerosis

  5007. PGNMi001-A (AG08C5)

    France Institut NeuroMyoGene - Pathophysiology and Genetics of Neuron and Muscle (INMG-PGNM) (PGNM)
    Disease:

    Normal (average)

  5008. PHAi003-A (PIDi003-A)

    Sweden Pan-Hammarström laboratory (PHA)
    Disease:

    Primary immunodeficiency

  5009. PHAi003-B (PIDi003-B)

    Sweden Pan-Hammarström laboratory (PHA)
    Disease:

    Primary immunodeficiency

  5010. PMUi001-A (Alice and BMACA-CT2-A)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal (average)

  5011. PMUi001-B (Betty and BMACA-CT2-B)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal (average)

  5012. PMUi001-C (Chantal and BMACA-CT2-C)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal (average)

  5013. PMUi002-A (Cornelius and UCB144-CT2-C)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal (average)

  5014. PMUi002-A-1 (UCB144-CT2-C DOCK2KO clone 19 and Cornelius DOCK2KO clone 19)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Severe combined immunodeficiency

  5015. PMUi002-A-2 (UCB144-CT2-C DOCK2KO clone 20 and Cornelius DOCK2KO clone 20)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Severe combined immunodeficiency

  5016. PMUi002-A-3 (Cornelius DOCK2KO clone 22 and UCB144-CT2-C DOCK2KO clone 22)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Severe combined immunodeficiency

  5017. PMUi002-B (Gustav and UCB144-CT1-G)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal (average)

  5018. PNUi004-A

    Japan Department of Psychiatry, Nagoya University Graduate School of Medicine (PNU)
    Disease:

    Schizophrenia

  5019. PNUi004-B

    Japan Department of Psychiatry, Nagoya University Graduate School of Medicine (PNU)
    Disease:

    Schizophrenia

  5020. PNUi004-C

    Japan Department of Psychiatry, Nagoya University Graduate School of Medicine (PNU)
    Disease:

    Schizophrenia

  5021. PNURCKi001-A (CK-iAT1)

    South Korea Pusan National University Yangsan Hospital, Rare Disease Center (PNURCK)
    Disease:

    Arts syndrome

  5022. PNURCKi002-A (CK-iCD1)

    South Korea Pusan National University Yangsan Hospital, Rare Disease Center (PNURCK)
    Disease:

    Citrin deficiency

  5023. PNURCKi003-A (CK-iDS1)

    South Korea Pusan National University Yangsan Hospital, Rare Disease Center (PNURCK)
    Disease:

    Desanto-shinawi syndrome

  5024. PNUSCRi001-A (GBA PD iPSC7)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Parkinson disease

  5025. PNUSCRi002-A (GBA PD iPSC9)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Parkinson disease

  5026. PNUSCRi003-A (GBA Gaucher iPSC1)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Gaucher disease

  5027. PNUSCRi004-A (GBA PD iPSC8)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Parkinson disease

  5028. PNUSCRi005-A

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Hunter syndrome

  5029. PNUSCRi006-A (Sanfilippo hiPSCs)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Sanfilippo syndrome

  5030. PNUYHi002-A

    South Korea Pusan National University Yangsan Hospital (PNUYH)
    Disease:

    Alzheimer's disease

  5031. PNUYHi003-A

    South Korea Pusan National University Yangsan Hospital (PNUYH)
    Disease:

    Neuronal intranuclear inclusion disease

  5032. PNUYHi004-A (GBA2A)

    South Korea Pusan National University Yangsan Hospital (PNUYH)
    Disease:

    Hereditary spastic paraplegia

  5033. PSXi015-A (RUCDRi002-A and TC-1133)

    United States Pluristyx (PSX)
    Disease:

    Normal (average)

  5034. PUFHi004-A (TMEM163 c.227T>C p.(Leu76Pro) iPSC)

    China Peking University First Hospital (PUFH)
    Disease:

    Leukodystrophy

  5035. PUMCi002-A (AF-iPSCs and C1)

    China Peking Union Medical College (PUMC)
    Disease:

    Normal (average)

  5036. PUMCi006-A

    China Peking Union Medical College (PUMC)
    Disease:

    Alzheimer disease

  5037. PUMCHi001-A (IPS-34)

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Familial partial lipodystrophy type 2

  5038. PUMCHi001-A-1 (IPS34-R-17)

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Familial partial lipodystrophy type 2

  5039. PUMCHi002-A (20180908R-AE3 and PUMCH-IRC)

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Restrictive cardiomyopathy

  5040. PUMCHi004-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Hereditary systemic amyloidosis 1

  5041. PUMCHi005-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Cardiac transthyretin amyloid deposition

  5042. PUMCHi019-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Autosomal dominant optic atrophy plus syndrome

  5043. PUMCHi020-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Aicardi-goutieres syndrome

  5044. PVDMMi001-A (NG2266)

    Italy Molecular Medicine Department - University of Pavia (unipv) (PVDMM)
    Disease:

    Joubert syndrome

  5045. PVDMMi002-A (NG5925)

    Italy Molecular Medicine Department - University of Pavia (unipv) (PVDMM)
    Disease:

    Joubert syndrome

  5046. PVDMMi003-A (NG2685)

    Italy Molecular Medicine Department - University of Pavia (unipv) (PVDMM)
    Disease:

    Joubert syndrome

  5047. PVDMMi004-A (NG4713)

    Italy Molecular Medicine Department - University of Pavia (unipv) (PVDMM)
    Disease:

    Joubert syndrome

  5048. QBRIi001-A (Ctr1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  5049. QBRIi001-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  5050. QBRIi001-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  5051. QBRIi002-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  5052. QBRIi002-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  5053. QBRIi002-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  5054. QBRIi005-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  5055. QBRIi005-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  5056. QBRIi005-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  5057. QBRIi006-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_psoriasis

  5058. QBRIi006-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_psoriasis

  5059. QBRIi006-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_psoriasis

  5060. QBRIi007-A (GLUT2 Mut-int iPSCs)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Fanconi-bickel syndrome

  5061. QBRIi009-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Central hypothyroidism

  5062. QBRIi013-A

    Qatar Qatar Biomedical Research Institute (QBRI)

  5063. QBRIi014-A (NDD01 and hiPSC_11080401_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  5064. QBRIi015-A (NDD04 and hiPSC_11080404_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  5065. QBRIi016-A (NDD05 and hiPSC_11080405_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  5066. QBRIi017-A (CtrlM and hiPSC_11080402_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  5067. QBRIi018-A (hiPSC_11080403_c1 and CtrlF)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  5068. QBRIi019-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  5069. QBRIi020-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  5070. QBRIi021-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  5071. QBRIi021-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  5072. QBRIi022-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  5073. QBRIi022-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  5074. QBRIi023-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  5075. QBRIi023-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  5076. QBRIi024-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  5077. QBRIi024-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  5078. QBRIi025-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  5079. QBRIi025-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  5080. QBRIi026-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  5081. QBRIi027-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  5082. QBRIi027-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  5083. RAUi001-A

    Armenia Russian-Armenian University (RAU)
    Disease:

    Normal (average)

  5084. RAUi001-B

    Armenia Russian-Armenian University (RAU)
    Disease:

    Normal (average)

  5085. RAUi001-C

    Armenia Russian-Armenian University (RAU)
    Disease:

    Normal (average)

  5086. RAUi002-A

    Armenia Russian-Armenian University (RAU)
    Disease:

    Familial mediterranean fever

  5087. RBi001-A (fb101 and RB101)

    United Kingdom R Biomedical (RB)
    Disease:

    Normal (average)

  5088. RCi004-A (PDSC-10 and RCi150)

    United Kingdom Roslin Cells (RC)
    Disease:

    Huntington disease

  5089. RCi004-B (RCi68 and PDSC-3)

    United Kingdom Roslin Cells (RC)
    Disease:

    Huntington disease

  5090. RCi005-A (FB71c4 and RCi171)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  5091. RCi006-A (FB69c4 and RCi169)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  5092. RCi007-A (FB70c1 and RCi170)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  5093. RCi007-C

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  5094. RCi009-A (Rci201 and FB73c6)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  5095. RCMGi001-A (P1L5)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  5096. RCMGi002-A (P7L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  5097. RCMGi004-A (P6L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  5098. RCMGi004-B (P6L8)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  5099. RCMGi005-A (P5L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  5100. RCMGi005-B (P5L5)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  5101. RCMGi006-A (VII_MAK_C)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Normal (average)

  5102. RCMGi007-A (P8L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  5103. RCMGi008-A (P9L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  5104. RCMGi009-A (P14L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Fibrodysplasia ossificans progressiva

  5105. RCMGi011-A (P10L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Mucopolysaccharidosis type ivb

    Disease:

    Autosomal recessive nonsyndromic deafness 12

  5106. RCMGi011-B (P10L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Mucopolysaccharidosis type ivb

    Disease:

    Autosomal recessive nonsyndromic deafness 12

  5107. RCMGi012-A (P11L3)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Maroteaux-lamy syndrome

  5108. RCMGi013-A (P2L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  5109. RCMGi014-A (P20L7)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Fibrodysplasia ossificans progressiva

  5110. RCMGi015-A (P16L4)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Glycogen storage disease i

  5111. RCMGi016-A (P17L16)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Glycogen storage disease i

  5112. RCMGi017-A (P12L3)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Normal (average)

  5113. RCMGi018-A (P22L5)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Duchenne muscular dystrophy

  5114. RCNSi003-A (2GMB7)

    Hungary RCNS-Institute of Molecular Life Sciences (RCNS)
    Disease:

    Normal (average)

  5115. RCPCMi002-A (HD76)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Huntington disease

  5116. RCPCMi003-A (ATXN1KCl2)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Spinocerebellar ataxia 1

  5117. RCPCMi004-A (Park14-4)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Obsolete_parkinson's disease

  5118. RCPCMi005-A (IPSP12-1)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Obsolete_parkinson's disease

  5119. RCPCMi007-A (IPSFF1S)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Normal (average)

  5120. RCPCMi007-A-1 (IPSFF1S deltab2m)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Normal (average)

  5121. RCPCMi008-A (IPS SCA17 sev cln4)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Spinocerebellar ataxia 17

  5122. RCPCMi009-A (IPSRG4S and UEF-3B)

    Finland Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Normal (average)

  5123. RCPCMi009-A-1 (IPSRG4S-206)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    X-linked intellectual disability, nascimento type

  5124. RCPCMi010-A (iPS 67-7)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    X-linked intellectual disability, nascimento type

  5125. RCPCMi011-A (IPSFIL24S)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Restrictive cardiomyopathy

  5126. RCPCMi011-B (IPSFIL23S)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Restrictive cardiomyopathy

  5127. RCPCMi012-A (CYFIP-MV-9R)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    West syndrome

  5128. RCPCMi013-A (IPSAVE2S)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Normal (average)

  5129. RCPCMi014-A (PBM022E5)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Normal (average)

  5130. RCPCMi014-B (PBM022E7)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Normal (average)

  5131. RCPCMi017-A (IPSCANVAS1E6)

    Russia Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Cerebellar ataxia, neuropathy, and vestibular areflexia syndrome

  5132. RCSIi001-A (iPDK)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Normal (average)

  5133. RCSIi002-A (iDFU8)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Obsolete_diabetes mellitus

  5134. RCSIi003-A (iNFF12)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Normal (average)

  5135. RCSIi004-A (iNFF14)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Normal (average)

  5136. RCSIi005-A (iDFF24)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Obsolete_diabetes mellitus

  5137. REGi001-A (LEB_M)

    France SAFE iPS Facility (REG)
    Disease:

    Bosch-boonstra-schaaf optic atrophy syndrome

  5138. REGi002-A (CHAP_P)

    France SAFE iPS Facility (REG)
    Disease:

    Bosch-boonstra-schaaf optic atrophy syndrome

  5139. REGi003-A (PIN_L)

    France SAFE iPS Facility (REG)
    Disease:

    Bosch-boonstra-schaaf optic atrophy syndrome

  5140. REGi004-A (MAR_N)

    France SAFE iPS Facility (REG)
    Disease:

    Bosch-boonstra-schaaf optic atrophy syndrome

  5141. REGi005-A (VER_C)

    France SAFE iPS Facility (REG)
    Disease:

    Bosch-boonstra-schaaf optic atrophy syndrome

  5142. REGi007-A (COL_T)

    France SAFE iPS Facility (REG)
    Disease:

    Bosch-boonstra-schaaf optic atrophy syndrome

  5143. REGUi001-A (IPS4FLV)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  5144. REGUi002-A (IPS6FLV)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  5145. REGUi009-A (myasthenic syndrome due to mutation in ColQ and hiPS 5-9016)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Congenital myasthenic syndrome

  5146. REGUi016-A (4F_Tie2_RNA190)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  5147. REGUi016-C (4F_Tie2_Sv190)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  5148. REGUi016-D (4F_PBMC_Sv190)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  5149. REGUi017-A (4F_Tie2_RNA191)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  5150. REGUi017-C (4F_Tie2_Sv191)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  5151. REGUi017-D (4F_PBMC_Sv191)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  5152. REGUi018-A (4F_Tie2_RNA192)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  5153. REGUi018-C (4F_Tie2_Sv192)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  5154. REGUi018-D (4F_PBMC_Sv192)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  5155. RFSCi001-A (RFSC3)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  5156. RFSCi002-A (RFSC4)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Age-related macular degeneration

  5157. RFSCi003-A (RFSC22)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  5158. RFSCi004-A (RFSC23)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Age-related macular degeneration

  5159. RFSCi005-A (RFSC18)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  5160. RFSCi006-A (RFSC19)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Age-related macular degeneration

  5161. RFSCi007-A (RFSC10)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  5162. RFSCi008-A (RFSC16)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  5163. RIi001-A (R.1.H.iPSC.1)

    Iran Royan Institute (RI)

  5164. RIi002-A (BOM.1.H.iPSC.1)

    Iran Royan Institute (RI)
    Disease:

    Normal (average)

  5165. RIi003-A (FHC.1.H.iPSC.3)

    Iran Royan Institute (RI)
    Disease:

    Familial hypercholesterolemia

  5166. RIi004-A (GSD.1.H.iPSC.7)

    Iran Royan Institute (RI)
    Disease:

    Glycogen storage disease

  5167. RIi005-A (TYR.1.H.iPSC.1)

    Iran Royan Institute (RI)
    Disease:

    Tyrosinemia type 1

  5168. RIi006-A (HER.1.H.iPSC.1)

    Iran Royan Institute (RI)
    Disease:

    Cholestasis

  5169. RIi007-A (R.1.H.iPSC.4)

    Iran Royan Institute (RI)

  5170. RIi008-A (R.1.H.iPSC.9)

    Iran Royan Institute (RI)

  5171. RIi009-A (RP2.H.iPSC.3)

    Iran Royan Institute (RI)
    Disease:

    Retinitis pigmentosa

  5172. RIi010-A (LCA.1.H.iPSC.1)

    Iran Royan Institute (RI)
    Disease:

    Leber congenital amaurosis

  5173. RIi011-A (USH.1.H.iPSC.6)

    Iran Royan Institute (RI)
    Disease:

    Usher syndrome

  5174. RIi012-A (RP.1.H.iPSC.2)

    Iran Royan Institute (RI)
    Disease:

    Retinitis pigmentosa

  5175. RIi013-A (ARMD.1.H.iPSC.2)

    Iran Royan Institute (RI)
    Disease:

    Obsolete_age-related macular degeneration

  5176. RIi014-A (LHON.1.H.iPSC.5)

    Iran Royan Institute (RI)
    Disease:

    Leber congenital amaurosis

  5177. RIi015-A (CNS.1.H.iPSC.10)

    Iran Royan Institute (RI)
    Disease:

    Crigler-najjar syndrome

  5178. RIi016-A (CNS.2.H.iPSC.7)

    Iran Royan Institute (RI)
    Disease:

    Crigler-najjar syndrome

  5179. UCSFi001-A-87

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Tuberous sclerosis 2

  5180. RMCGENi005-A

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  5181. RMCGENi005-A-1

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  5182. SCTCi017-A-1

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  5183. SCTCi018-A-1

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  5184. RMCGENi020-A (IPS15-00004)

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  5185. RMCGENi021-A (IPS22-00087)

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  5186. SCTCi043-A-1 (iPS23-00086 clE2 and fIPS_DM1Rescue_P1 clE2)

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Myotonic dystrophy type 1

  5187. SCTCi044-A-1 (iPS24-00086 clB5 and fiPS_DM1Rescue_P2 clB5)

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Myotonic dystrophy type 1

  5188. SCTCi045-A-1 (iPS24-00085 clE3 and fIPS_DM1Rescue_P3 clE3)

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Myotonic dystrophy type 1

  5189. RNRMUi001-A (RDEB-iPSC-d1)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Epidermolysis bullosa dystrophica, autosomal recessive

  5190. RNRMUi002-A (RDEB-iPSC-d2)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Epidermolysis bullosa dystrophica, autosomal recessive

  5191. RNRMUi003-A (RDEB-iPSC-d3A)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Epidermolysis bullosa dystrophica, autosomal recessive

  5192. KUIFMSi004-A-1 (hPSC MPP8 Neon Green)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Normal (average)

  5193. RNRMUi005-A (EB-iPSC-d4 and RDEB-iPSC-d4)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Recessive dystrophic epidermolysis bullosa

    Disease:

    Epidermolysis bullosa simplex

  5194. RNRMUi006-A (RDEB-IPSC-d10)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Recessive dystrophic epidermolysis bullosa

  5195. RNRMUi007-A (EBS-iPSC-d12)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Epidermolysis bullosa simplex 2f, with mottled pigmentation

  5196. RTIBDi001-A (MCND-TENS2)

    United States Regenerative Therapies for Inherited Blood Disorder (RTIBD)
    Disease:

    Normal (average)

  5197. RUCDRi002-A (TC-113, 50-001-21, 50-001-21.P20_10, ND50038, LiPSC-GR1.1 and TC-1133)

    United States RUCDR Infinite Biologics (RUCDR)
    Disease:

    Normal (average)

  5198. SANi011-A (PE1S40 cl.D and FLI1 clone D)

    Netherlands Sanquin (SAN)
    Disease:

    Bleeding disorder, platelet-type, 21

  5199. SANi012-A (ETV6 cl.6 and PE1L103 cl.6)

    Netherlands Sanquin (SAN)
    Disease:

    Thrombocytopenia 5

  5200. SANi013-A (TRACER #P5 clone F)

    Netherlands Sanquin (SAN)
    Disease:

    Diamond-blackfan anemia

  5201. SAPi002-A (ALS I, ALS I–FUS-R514S/wt and FUS-R514S/wt)

    Italy Sapienza University of Rome (SAP)
    Disease:

    Amyotrophic lateral sclerosis

  5202. SAPi003-A (ALS II, FUS-R521C/wt and ALS II–FUS-R521C/wt)

    Italy Sapienza University of Rome (SAP)
    Disease:

    Amyotrophic lateral sclerosis

  5203. SAPi004-A (ALS III, TDP43-A382T/A382T and ALS III-TDP43-A382T/A382T)

    Italy Sapienza University of Rome (SAP)
    Disease:

    Amyotrophic lateral sclerosis

  5204. SBIi006-A (SC102A-1)

    United States System Biosciences (SBI)
    Disease:

    Normal (average)

  5205. SBRIi001-A

    France Stem Cell and Brain Research - U1208 INSERM (SBRI)
    Disease:

    Normal (average)

  5206. SBWCHi001-A

    China Shenzhen Baoan Women's and Children's Hospital, Jinan University (SBWCH)
    Disease:

    Ctnnb1 gene mutation

  5207. SCAUi001-A

    China South China Agricultural University (SCAU)
    Disease:

    Normal (average)

  5208. SCAUi001-A-1

    China South China Agricultural University (SCAU)
    Disease:

    Cone-rod dystrophy

  5209. SCAUi001-A-2

    China South China Agricultural University (SCAU)
    Disease:

    Retinitis pigmentosa

  5210. SCHi001-A

    South Korea Severance Children’s Hospital (SCH)
    Disease:

    Adrenoleukodystrophy

  5211. SCHi001-A-1 (AMN5-Corrected iPSC)

    South Korea Severance Children’s Hospital (SCH)
    Disease:

    Adrenoleukodystrophy

  5212. SCIKFi001-A (D3-iR-2)

    Indonesia Stem Cell and Cancer Institute, PT. Kalbe Farma Tbk. (SCIKF)
    Disease:

    Normal (average)

  5213. SCIKFi001-B (D3-iE)

    Indonesia Stem Cell and Cancer Institute, PT. Kalbe Farma Tbk. (SCIKF)
    Disease:

    Normal (average)

  5214. SCMCi001-A

    China Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine (SCMC)
    Disease:

    Normal (average)

  5215. SCMCi001-A-1

    China Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine (SCMC)
    Disease:

    Congenital heart disease

  5216. SCTi001-A (STiPS-F016)

    Canada STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  5217. SCTi002-A (STiPS-M001)

    Canada STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  5218. SCTi003-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  5219. SCTi003-A-1

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Alzheimer's disease

  5220. SCTi003-A-2

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Alzheimer's disease

  5221. SCTi003-A-3

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Stargardt disease

  5222. SCTi004-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  5223. SCTi005-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  5224. SCTi006-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  5225. SCTCi008-A (IPS17-00095)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  5226. SCTCi009-A (IPS17-00097)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  5227. SCTCi010-A (IPS17-00041)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  5228. SCTCi011-A (IPS18-00072)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Obsolete_age-related macular degeneration

  5229. SCTCi012-A (IPS19-00027)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Obsolete_age-related macular degeneration

  5230. SCTCi013-A (IPS19-00053)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Obsolete_age-related macular degeneration

  5231. SCTCi014-A (IPS17-00056)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  5232. SCTCi014-A-1 (IPS17-00056 Crispr clone O5)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  5233. SCTCi015-A (IPS19-00051)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  5234. SCTCi015-A-1 (IPS19-00051 Crispr clone H6)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  5235. SCTCi016-A (IPS18-00092)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Leber congenital amaurosis

  5236. SCTCi017-A (IPS15-00006)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Stargardt disease

  5237. SCTCi018-A (IPS15-00007)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Stargardt disease

  5238. SCTCi020-A (IPS17-00028)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  5239. SCTCi021-A (IPS17-00027)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  5240. SCTCi022-A (IPS17-00042)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  5241. SCTCi023-A (IPS17-00063)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Self-limited familial neonatal epilepsy

  5242. SCTCi024-A (IPS18-00047)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  5243. SCTCi025-A (IPS18-00095)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Self-limited familial neonatal epilepsy

  5244. SCTCi026-A (IPS22-00005)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Pyridoxine-dependent epilepsy

  5245. SCTCi027-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Pyridoxine-dependent epilepsy

  5246. SCTCi028-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Pyridoxine-dependent epilepsy

  5247. SCTCi029-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Pyridoxine-dependent epilepsy

  5248. SCTCi030-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Glutaric acidemia type 1

  5249. SCTCi031-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Glutaric acidemia type 1

  5250. SCTCi032-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Glutaric acidemia type 1

  5251. SCTCi033-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Glutaric acidemia type 1

  5252. SCTCi037-A (IPS19-00015)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  5253. SCTCi037-A-1 (EPC26.1.1)

    Belgium Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  5254. SCTCi039-A (IPS19-00092)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  5255. SCTCi039-A-1 (NGC22.3.369)

    Belgium Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  5256. SCTCi041-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  5257. SCTCi042-A (IPS17-00036)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  5258. SCTCi043-A (fIPS_DM1_P1 cl1 and iPS19-00072 cl1)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Myotonic dystrophy type 1

  5259. SCTCi044-A (fIPS_DM1_P2 cl1 and iPS19-00073 cl1)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Myotonic dystrophy type 1

  5260. SCTCi045-A (iPS21-00148 cl1 and fIPS_DM1_P3 cl1)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Myotonic dystrophy type 1

  5261. SCTCi046-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Corneal dystrophy, fuchs endothelial, 3

  5262. SCTCi047-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Corneal dystrophy, fuchs endothelial, 3

  5263. SCVIi030-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  5264. SCVIi031-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  5265. SCVIi036-A (SCVI248)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  5266. SCVIi037-A (SCVI672)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  5267. SCVIi049-A (SCVI104)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5268. SCVIi050-A (SCVI2486)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5269. SCVIi051-A (477)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5270. SCVIi053-A (2021)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5271. SCVIi055-A (SCVI868 and SCVI-868)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5272. SCVIi056-A (SCVI956 and SCVI-956)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5273. SCVIi057-A (SCVI-975 and SCVI975)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5274. SCVIi059-A (SCVIi2413)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5275. SCVIi060-A (SCVi2506)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5276. SCVIi061-A (SCVI2149C1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome

  5277. SCVIi062-A (SCVI2150c1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome

  5278. SCVIi066-A (SCVI2047)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Cardiac attr amyloidosis

  5279. SCVIi067-A (SCVI2742)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Cardiac attr amyloidosis

  5280. SCVIi073-A (SCVIi574C2)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5281. SCVIi074-A (SCVIi599C1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5282. SCVIi075-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Obsolete_spinal muscular atrophy

  5283. SCVIi076-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Obsolete_spinal muscular atrophy

  5284. SCVIi077-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  5285. SCVIi078-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  5286. SCVIi079-A (SCVI167 and PHBI-ST-036)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Idiopathic pulmonary hypertension

  5287. SCVIi080-A (PHBI-ST-040 and SCVI171)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Idiopathic pulmonary hypertension

  5288. SCVIi081-A (SCVI2535)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5289. SCVIi082-A (SCVI2838)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5290. SCVIi083-A (SCVI2655)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5291. SCVIi084-A (SCVI2591)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5292. SCVIi085-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Obsolete_down syndrome

  5293. SCVIi086-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Obsolete_down syndrome

  5294. SCVIi087-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Duchenne muscular dystrophy

  5295. SCVIi088-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Duchenne muscular dystrophy

  5296. SCVIi091-A (SCVI2617)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hereditary systemic amyloidosis 1

  5297. SCVIi092-A (SCVI2628)

    United States Stanford Cardiovascular Institute (SCVI)

  5298. SCVIi096-A (SCVI-675fs1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5299. SCVIi097-A (SCVI-675fs2)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5300. SCVIi098-A (SCVI-675fs3)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5301. SCVIi099-A (SCVI-675fs4)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5302. SCVIi100-A (SCVI2009A)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5303. SCVIi101-A (SCVI926A)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5304. SCVIi104-A (SCVIi2996)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Li-fraumeni syndrome

  5305. SCVIi105-A (SCVIi3001)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Li-fraumeni syndrome

  5306. SCVIi106-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Williams syndrome

  5307. SCVIi107-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Williams syndrome

  5308. SCVIi108-A (SCVI2767)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Familial hypercholesterolemia

  5309. SCVIi109-A (SCVI3020)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Familial hypercholesterolemia

  5310. SCVIi110-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome 1

  5311. SCVIi111-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome 1

  5312. SCVIi114-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Lynch syndrome

  5313. SCVIi115-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Lynch syndrome

  5314. SCVIi116-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Phace syndrome

  5315. SCVIi117-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Phace syndrome

  5316. SCVIi118-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Phace syndrome

  5317. SCVIi121-A (SCVI 488)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5318. SCVIi123-A (SCVI 2176)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5319. SCVIi124-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Loeys-dietz syndrome 1

  5320. SCVIi125-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Loeys-dietz syndrome 1

  5321. SCVIi126-A (SCVI2899)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Facioscapulohumeral muscular dystrophy

  5322. SCVIi127-A (SCVI2830)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Facioscapulohumeral dystrophy

  5323. SCVIi128-A (SCVI766)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Marfan syndrome

  5324. SCVIi129-A (SCVI2454)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Marfan syndrome

  5325. SCVIi132-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5326. SCVIi134-A (SCVI 692)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Myotonic dystrophy type 1

  5327. SCVIi135-A (SCVI3161)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5328. SCVIi136-A (SCVI3171)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5329. SCVIi137-A (SCVI 770)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Myotonic dystrophy type 1

  5330. SCVIi138-A (SCVI2741)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Thoracic aortic aneurysm

  5331. SCVIi139-A (SCVI2925)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Thoracic aortic aneurysm

  5332. SCVIi140-A (iPSC3503)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5333. SCVIi141-A (iPSC3880)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5334. SCVIi142-A (SCVI2900)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Pten hamartoma tumor syndrome

  5335. SCVIi143-A (SCVI3215)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Pten hamartoma tumor syndrome

  5336. SCVIi145-A (SCVI997)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Emery-dreifuss muscular dystrophy

  5337. SCVIi146-A (SCVI3443)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  5338. SCVIi150-A (GSB-L159)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Marfan syndrome

  5339. SCVIi151-A (GSB-L2728)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Marfan syndrome

  5340. SCVIi152-A (3135)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypokalemic periodic paralysis

  5341. SCVIi153-A (3136)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypokalemic periodic paralysis

  5342. SCVIi154-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5343. SCVIi155-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5344. SCVIi156-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5345. SCVIi157-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5346. SCVIi158-A (SCVI2930)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5347. SCVIi159-A (SCVI3070)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5348. SCVIi162-A (SCVI3067)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5349. SCVIi163-A (SCVI3354)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5350. SCVIi166-A (3041)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hereditary hemorrhagic telangiectasia

  5351. SCVIi167-A (3806)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hereditary hemorrhagic telangiectasia

  5352. SCVIi170-A (SCVI3138)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5353. SCVIi171-A (SCVI2254)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5354. SCVIi172-A (SCVI3308)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Immune checkpoint inhibitor-related myocarditis

  5355. SCVIi173-A (SCVI3766)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5356. SCVIi174-A (SCVIC7)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5357. SDASi001-A

    China Qilu University of Technology(Shandong Academy of Sciences) (SDAS)
    Disease:

    Schimke immuno-osseous dysplasia

  5358. SDCHi001-A

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Normal (average)

  5359. SDCHi005-A (DEPDC5-ZHW)

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Epilepsy

  5360. SDCHi007-A (RY-5)

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Epilepsy

  5361. SDCHi008-A (CX2)

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Epilepsy

  5362. SDCHi009-A (RY6)

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Epilepsy

  5363. SDCHi011-A

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Normal (average)

  5364. SDHi001-A (MVPSDHi001)

    China The Fourth Affiliated Hospital of Soochow University(Suzhou Dushu Lake Hospital) (SDH)
    Disease:

    Mitral valve prolapse

  5365. SDPHi002-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Lung cancer

  5366. SDPHi003-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Normal (average)

  5367. SDPHi004-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Normal (average)

  5368. SDPHi005-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Normal (average)

  5369. SDPHi006-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Normal (average)

  5370. SDPHi007-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Alagille syndrome

  5371. SDQLCHi028-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Xia-gibbs syndrome

  5372. SDQLCHi030-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Lesch-nyhan syndrome

  5373. SDQLCHi043-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)

  5374. SDQLCHi050-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Normal (average)

  5375. SDQLCHi054-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Intellectual developmental disorder, autosomal dominant 5

  5376. SDQLCHi059-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Congenital disorder of deglycosylation

  5377. SDQLCHi061-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Carbamoyl phosphate synthetase i deficiency disease

  5378. SDQLCHi062-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Focal segmental glomerulosclerosis 7

  5379. SDQLCHi063-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Maturity-onset diabetes of the young type 2

  5380. SDQLCHi064-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Canavan disease

  5381. SDQLCHi065-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Down syndrome

  5382. SDQLCHi066-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Th-deficient dopa-responsive dystonia

  5383. SDQLCHi067-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Subcortical band heterotopia

  5384. SDQLCHi068-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Immunodeficiency 14a, autosomal dominant

  5385. SDQLCHi072-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Autism spectrum disorder due to auts2 deficiency

  5386. SDQLCHi073-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Cockayne syndrome

  5387. SDQLCHi079-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Johanson-blizzard syndrome

  5388. SDQLCHi080-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Gm1 gangliosidosis

  5389. SDQLCHi081-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Rahman syndrome

  5390. SDQLCHi083-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Autosomal recessive cutis laxa type iid

  5391. SDQLCHi084-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Clark-baraitser syndrome

  5392. SDQLCHi087-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Normal (average)

  5393. SDUBMSi001-A

    China School of Basic Medical Sciences, Shandong University (SDUBMS)
    Disease:

    Hereditary spastic paraplegia

  5394. SDUCHi001-A

    China Children’s Hospital Affiliated to Shandong University (SDUCH)
    Disease:

    Normal (average)

  5395. SDZFYi001-A

    China Shandong Academy of Occupational Health and Occupational Medicine (SDZFY)
    Disease:

    Normal (average)

  5396. SEUi001-A

    China Southeast University (SEU)
    Disease:

    Normal (average)

  5397. SFMUi001-A

    China Shandong First Medical University (SFMU)
    Disease:

    Usher syndrome type 2

  5398. SFPHi001-A

    China Shanghai Fifth People’s Hospital (SFPH)
    Disease:

    Hereditary antithrombin deficiency

  5399. SHCDNi001-A (SHCDN001)

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Mitochondrial dna depletion syndrome

  5400. SHCDNi002-A (SHCDN002)

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Fg syndrome

    Disease:

    Lujan-fryns syndrome

  5401. SHCDNi003-A

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Allan-herndon-dudley syndrome

  5402. SHCDNi006-A (SHCDN006)

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Obsolete_epilepsy

  5403. SHCDNi007-A

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Pyruvate carboxylase deficiency

  5404. SHCDNRi001-A (IPS-51)

    China Shanghai Children's Hospital, Department of Nephrology and Rheumatology (SHCDNR)
    Disease:

    Alport syndrome

  5405. SHCHNDi002-A

    China Shanghai Children's Hospital (SHCHND)
    Disease:

    Infantile liver failure syndrome 2

  5406. SHEHi002-A (iPS36)

    China Shanghai East Hospital (SHEH)
    Disease:

    Long qt syndrome 8

  5407. SHEHDNi001-A

    China Department of Neurology (SHEHDN)
    Disease:

    Obsolete_alzheimer's disease

  5408. SHEHDNi002-A (KY03AP)

    China Department of Neurology (SHEHDN)
    Disease:

    Parkinson disease

  5409. SHETi001-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Floating-harbor syndrome

  5410. SHETi002-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Arrhythmia

  5411. SHETi003-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  5412. SHETi004-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Left bundle branch block artifact

  5413. SHETi005-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Normal (average)

  5414. SHFDi001-A (SHFD-1)

    China Shanghai Stomatological Hospital, Fudan University, Shanghai, China (SHFD)
    Disease:

    Ankylosing spondylitis

  5415. SHIPMi001-A

    China Shanghai Institute of Precision Medicine (SHIPM)
    Disease:

    Hypertrophic cardiomyopathy

  5416. SHIPMi002-A

    China Shanghai Institute of Precision Medicine (SHIPM)
    Disease:

    Normal (average)

  5417. SHTCMi001-A

    China Affiliated Hospital of Shandong University of Traditional Chinese Medicine (SHTCM)
    Disease:

    X-linked alport syndrome

  5418. SHUPLi001-A (IPS-14)

    China Shanghai University of Political Science and Law (SHUPL)
    Disease:

    Normal (average)

  5419. SHUPLi002-A (iPS-26)

    China Shanghai University of Political Science and Law (SHUPL)
    Disease:

    Normal (average)

  5420. SHUTCMi001-A (i0809-B1073B)

    China Shanghai University of Traditional Chinese Medicine (SHUTCM)
    Disease:

    Lung squamous cell carcinoma

  5421. SIAISi001-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Obsolete_alzheimer's disease

  5422. SIAISi002-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5423. SIAISi003-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Obsolete_alzheimer's disease

  5424. SIAISi004-A (ZYF)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Obsolete_alzheimer's disease

  5425. SIAISi006-A (JJY)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Alzheimer's disease

  5426. SIAISi007-A (ZSJ)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Alzheimer's disease

  5427. SIAISi008-A (ZMY)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Obsolete_alzheimer's disease

  5428. SIAISi009-A (YJP)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Mild cognitive impairment

  5429. SIAISi010-A (16F0040)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5430. SIAISi011-A (NZM)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5431. SIAISi012-A (QHL)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5432. SIAISi016-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Alzheimer's disease

  5433. SIAISi017-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5434. SIAISi018-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5435. SIAISi019-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5436. SIAISi020-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Mild cognitive impairment

  5437. SIAISi021-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Obsolete_alzheimer's disease

  5438. SIAISi022-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Alzheimer's disease

  5439. SIGi001-A (IPSC0028 parental and SAMEA4447455)

    United States Sigma-Aldrich (SIG)
    Disease:

    Normal (average)

  5440. SIGi001-A-1 (iPSC0028 SLC17A7/GFP E3)

    United States Sigma-Aldrich (SIG)
    Disease:

    Normal (average)

  5441. SIGi001-A-2 (iPSC0028 SLC17A7/GFP C3)

    United States Sigma-Aldrich (SIG)
    Disease:

    Normal (average)

  5442. SIGi001-A-3 (iPSC0028 MAPT P301L C4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5443. SIGi001-A-4 (iPSC0028 MAPT P301L D4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5444. SIGi001-A-5 (iPSC0028 MAPT P301S 1C9C4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5445. SIGi001-A-6 (iPSC0028 MAPT P301S 1B9C9)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5446. SIGi001-A-7 (iPSC0028 MAPT P301S 2G2B7)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5447. SIGi001-A-8 (iPSC0028 MAPT P301S+Ex10+16/Clone 7D11A7)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  5448. SIGi001-A-9 (iPSC0028 MAPT P301S+Ex10+16/Clone 7H6A1)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  5449. SIGi001-A-10 (iPSC0028 MAPT P301S+Ex10+16/Clone 7G4A8)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  5450. SIGi001-A-11 (iPSC0028 MAPT P301S+Ex10+16/Clone 7C6A4 and SAMEA4451118)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  5451. SIGi001-A-12 (iPSC0028 - BiAllelic MAPT_Ex10+16T/Clone 1F5-D12 and SAMEA104237570)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5452. SIGi001-A-13 (iPSC0028 – MonoAllelic MAPT_Ex10+16T/Clone 1D01-11)

    United States Sigma-Aldrich (SIG)
    Disease:

    Alzheimer disease

  5453. SIPDi001-A (Li-Campeau syndrome)

    China Shaanxi Institute of Pediatric Diseases (SIPD)
    Disease:

    Li-campeau syndrome

  5454. SJTUi003-A

    China Shanghai Jiao Tong University School of Medicine (SJTU)
    Disease:

    Alzheimer's disease

  5455. SJTUGHi001-A

    China Shanghai General Hospital (SJTUGH)
    Disease:

    Retinitis pigmentosa

  5456. SJTUGHi002-A

    China Shanghai General Hospital (SJTUGH)
    Disease:

    Retinitis pigmentosa

  5457. SJTUGHi004-A

    China Shanghai General Hospital (SJTUGH)
    Disease:

    Best vitelliform macular dystrophy

  5458. SJTUXHi001-A

    China Shanghai Xinhua Hospital (SJTUXH)
    Disease:

    Autism

  5459. SJTUXHi002-A

    China Shanghai Xinhua Hospital (SJTUXH)
    Disease:

    Autism

  5460. SJTUXHi003-A

    China Shanghai Xinhua Hospital (SJTUXH)
    Disease:

    Familial exudative vitreoretinopathy

  5461. SJTUXHi004-A

    China Shanghai Xinhua Hospital (SJTUXH)
    Disease:

    Retinoblastoma

  5462. SKi001-A (PGPC3-75 and SK1)

    Canada Hospital for Sick Children (SK)
    Disease:

    Normal (average)

  5463. SKi003-A (PGPC17-11 and SK2)

    Canada Hospital for Sick Children (SK)
    Disease:

    Normal (average)

  5464. SKi004-A (PGPC14-26 and SK4)

    Canada Hospital for Sick Children (SK)
    Disease:

    Normal (average)

  5465. SKLOi004-A

    China State Key Laboratory of Ophthalmology (SKLO)
    Disease:

    Retinoblastoma

  5466. SKLOi004-B

    China State Key Laboratory of Ophthalmology (SKLO)
    Disease:

    Retinoblastoma

  5467. SKLOi005-A

    China State Key Laboratory of Ophthalmology (SKLO)
    Disease:

    Leber congenital amaurosis

  5468. SKLOi005-B

    China State Key Laboratory of Ophthalmology (SKLO)
    Disease:

    Leber congenital amaurosis

  5469. SKLRMi001-A

    China State Key Laboratory of Reproductive Medicine, Nanjing Medical University (SKLRM)
    Disease:

    Androgen insensitivity syndrome

  5470. SKLRMi001-A-1 (AR repaired iPSCs)

    China State Key Laboratory of Reproductive Medicine, Nanjing Medical University (SKLRM)
    Disease:

    Androgen insensitivity syndrome

  5471. SMBCi002-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Clubfoot

  5472. SMBCi009-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Obsolete_familial hypercholesterolemia

  5473. SMBCi010-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Multiple osteochondromas

  5474. SMBCi011-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Prader-willi syndrome

  5475. SMBCi013-A (WD-iPSC)

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Hepatolenticular degeneration

  5476. SMBCi014-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Osteogenesis imperfecta

  5477. SMBCi018-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Clubfoot

  5478. SMBCi022-A (5003)

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Fabry disease

  5479. SMCPGHi001-A (SMCPGHi-ABCA3)

    China The Seven Medical Center of PLA General Hospital (SMCPGH)
    Disease:

    Pulmonary surfactant metabolism dysfunction-3

  5480. SMUSHi002-A

    China Southern Medical University Shenzhen hospital (SMUSH)
    Disease:

    Normal (average)

  5481. SMUSHi003-A

    China Southern Medical University Shenzhen hospital (SMUSH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  5482. SMUSHi005-A

    China Southern Medical University Shenzhen hospital (SMUSH)
    Disease:

    X-linked dominant hypophosphatemic rickets

  5483. SMUSHi006-A

    China Southern Medical University Shenzhen hospital (SMUSH)
    Disease:

    Amyotrophic lateral sclerosis

  5484. SNUHBBi001-A (SNUHBB2009_iPSC_C1)

    South Korea Seoul National University Hospital Dementia Brain Bank (SNUHBB)
    Disease:

    Parkinson disease

  5485. SNUHBBi002-A (SNUHBB2112_iPSC_C1)

    South Korea Seoul National University Hospital Dementia Brain Bank (SNUHBB)
    Disease:

    Alzheimer's disease

  5486. SNUHBBi003-A (SNUHBB2205_iPSC_C1)

    South Korea Seoul National University Hospital Dementia Brain Bank (SNUHBB)
    Disease:

    Pancreatic cancer

  5487. SPHi001-A (SLEi002HZY)

    China Shenzhen People's Hospital (SPH)
    Disease:

    Systemic lupus erythematosus

  5488. SPPHIi003-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)

  5489. SPPHIi004-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)
    Disease:

    Alzheimer disease

  5490. SPPHIi005-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)
    Disease:

    Normal (average)

  5491. SPPHIi006-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)

  5492. SPPHIi007-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)
    Disease:

    Normal (average)

  5493. SSMCi001-A

    China The Fourth People's Hospital of Shenzhen (Shenzhen Samii Medical Center) (SSMC)
    Disease:

    Dilated cardiomyopathy

  5494. SSMCi002-A

    China The Fourth People's Hospital of Shenzhen (Shenzhen Samii Medical Center) (SSMC)
    Disease:

    Dilated cardiomyopathy

  5495. STBCi004-A (SFC832-03-19)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5496. STBCi004-B (SFC832-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5497. STBCi004-B-1 (SFC832-03-06 LRRK2WT/WT C47)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5498. STBCi004-C (SFC832-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5499. STBCi005-A (SFC833-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5500. STBCi005-B (SFC833-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5501. STBCi005-C (SFC833-03-14)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5502. STBCi006-A (SFC140-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5503. STBCi007-A (SFC855-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5504. STBCi007-B (SFC855-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5505. STBCi007-C (SFC855-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5506. STBCi009-A (SFC801-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5507. STBCi009-B (SFC801-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5508. STBCi009-C (SFC801-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5509. STBCi010-A (SFC802-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5510. STBCi011-A (SFC803-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5511. STBCi011-B (SFC803-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5512. STBCi011-C (SFC803-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5513. STBCi012-A (SFC805-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5514. STBCi012-B (SFC805-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5515. STBCi012-C (SFC805-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5516. STBCi013-A (SFC807-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5517. STBCi013-B (SFC807-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5518. STBCi014-A (SFC808-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5519. STBCi014-B (SFC808-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5520. STBCi014-C (SFC808-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5521. STBCi015-A (SFC809-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5522. STBCi015-B (SFC809-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5523. STBCi015-C (SFC809-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5524. STBCi016-A (SFC810-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5525. STBCi016-B (SFC810-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5526. STBCi016-C (SFC810-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5527. STBCi017-A (SFC811-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5528. STBCi017-B (SFC811-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5529. STBCi017-C (SFC811-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5530. STBCi018-A (SFC815-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5531. STBCi018-B (SFC815-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5532. STBCi018-C (SFC815-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5533. STBCi019-A (SFC828-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5534. STBCi019-B (SFC828-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5535. STBCi019-C (SFC828-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5536. STBCi020-A (SFC800-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5537. STBCi020-B (SFC800-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5538. STBCi023-A (SFC829-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5539. STBCi023-B (SFC829-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5540. STBCi023-C (SFC829-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5541. STBCi024-A (SFC831-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5542. STBCi024-B (SFC831-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5543. STBCi024-C (SFC831-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5544. STBCi025-A (SFC834-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5545. STBCi025-B (SFC834-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5546. STBCi025-C (SFC834-03-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5547. STBCi026-A (SFC840-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5548. STBCi026-A-1 (SFC840-03-03 LRRK2-/-D10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5549. STBCi026-A-2 (SFC840-03-03 LRRK2-/-C11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5550. STBCi026-A-3 (SFC840-03-03 LRRK2 WT/R1441C H3)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5551. STBCi026-A-4 (SFC840-03-03-PITX3-GFP)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5552. STBCi026-B (SFC840-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5553. STBCi026-C (SFC840-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5554. STBCi026-D (SFC840-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5555. STBCi027-A (SFC017-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5556. STBCi027-B (SFC017-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5557. STBCi028-A (SFC018-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5558. STBCi028-B (SFC018-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5559. STBCi028-C (SFC018-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5560. STBCi029-A (SFC020-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5561. STBCi029-B (SFC020-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5562. STBCi030-A (SFC023-03-24)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5563. STBCi030-B (SFC023-03-43)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5564. STBCi031-A (SFC024-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5565. STBCi031-B (SFC024-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5566. STBCi031-C (SFC024-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5567. STBCi032-A (SFC042-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5568. STBCi032-B (SFC042-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5569. STBCi033-A (SFC084-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5570. STBCi033-B (SFC084-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5571. STBCi033-C (SFC084-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5572. STBCi034-A (SFC091-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5573. STBCi034-B (SFC091-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5574. STBCi035-A (SFC813-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5575. STBCi035-B (SFC813-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5576. STBCi035-C (SFC813-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5577. STBCi036-A (SFC814-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5578. STBCi037-A (SFC816-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5579. STBCi037-B (SFC816-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5580. STBCi037-C (SFC816-03-13)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5581. STBCi038-A (SFC011-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5582. STBCi038-B (SFC011-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5583. STBCi038-C (SFC011-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5584. STBCi039-A (SFC062-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5585. STBCi039-B (SFC062-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5586. STBCi039-C (SFC062-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5587. STBCi040-A (SFC029-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5588. STBCi040-B (SFC029-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5589. STBCi040-C (SFC029-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5590. STBCi041-A (SFC081-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5591. STBCi041-B (SFC081-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5592. STBCi041-C (SFC081-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5593. STBCi042-A (SFC848-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5594. STBCi042-B (SFC848-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5595. STBCi042-C (SFC848-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5596. STBCi043-A (SFC120-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5597. STBCi043-B (SFC120-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5598. STBCi043-C (SFC120-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5599. STBCi044-A (SFC841-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5600. STBCi044-B (SFC841-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5601. STBCi045-A (SFC039-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5602. STBCi045-B (SFC039-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5603. STBCi045-C (SFC039-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5604. STBCi046-A (SFC021-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5605. STBCi046-B (SFC021-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5606. STBCi047-A (SFC043-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5607. STBCi047-B (SFC043-03-13)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5608. STBCi048-A (SFC014-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5609. STBCi048-B (SFC014-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5610. STBCi048-C (SFC014-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5611. STBCi049-A (SFC040-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5612. STBCi049-B (SFC040-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5613. STBCi049-C (SFC040-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5614. STBCi050-A (SFC041-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5615. STBCi050-B (SFC041-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5616. STBCi050-C (SFC041-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5617. STBCi051-A (SFC056-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5618. STBCi051-B (SFC056-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5619. STBCi051-C (SFC056-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5620. STBCi052-A (SFC086-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5621. STBCi052-B (SFC086-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5622. STBCi052-C (SFC086-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5623. STBCi053-A (SFC089-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5624. STBCi053-B (SFC089-03-55)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5625. STBCi053-C (SFC089-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5626. STBCi054-A (SFC010-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5627. STBCi054-B (SFC010-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5628. STBCi055-A (SFC026-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5629. STBCi055-B (SFC026-04-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5630. STBCi055-C (SFC026-04-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5631. STBCi056-A (SFC064-03-39)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5632. STBCi056-B (SFC064-03-42)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5633. STBCi056-C (SFC064-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5634. STBCi057-A (SFC065-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5635. STBCi057-B (SFC065-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5636. STBCi057-C (SFC065-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5637. STBCi058-A (SFC012-04-20)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5638. STBCi058-B (SFC012-04-30)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5639. STBCi058-C (SFC012-04-31)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5640. STBCi059-A (SFC015-01-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5641. STBCi059-B (SFC015-01-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5642. STBCi059-C (SFC015-01-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5643. STBCi060-A (SFC038-07-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5644. STBCi060-B (SFC038-07-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5645. STBCi060-C (SFC038-07-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5646. STBCi061-A (SFC850-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5647. STBCi062-A (SFC851-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5648. STBCi063-A (SFC856-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5649. STBCi063-B (SFC856-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5650. STBCi063-C (SFC856-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5651. STBCi064-A (SFC180-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5652. STBCi065-A (SFC853-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5653. STBCi066-A (SFC854-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5654. STBCi067-A (SFC855-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5655. STBCi068-A (SFC035-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5656. STBCi068-B (SFC035-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5657. STBCi068-C (SFC035-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5658. STBCi069-A (SFC050-03-21)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5659. STBCi069-B (SFC050-03-22)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5660. STBCi069-C (SFC050-03-20)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5661. STBCi070-A (SFC052-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5662. STBCi070-B (SFC052-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5663. STBCi071-A (SFC057-07-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5664. STBCi071-B (SFC057-07-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5665. STBCi071-C (SFC057-07-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5666. STBCi072-A (SFC058-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5667. STBCi072-B (SFC058-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5668. STBCi072-C (SFC058-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5669. STBCi073-A (SFC106-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5670. STBCi073-B (SFC106-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5671. STBCi074-A (SFC109-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5672. STBCi074-B (SFC109-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5673. STBCi074-C (SFC109-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5674. STBCi075-A (SFC129-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5675. STBCi075-B (SFC129-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5676. STBCi075-C (SFC129-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5677. STBCi076-A (SFC134-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5678. STBCi077-A (SFC136-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5679. STBCi077-B (SFC136-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5680. STBCi077-C (SFC136-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5681. STBCi078-A (SFC013-07-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5682. STBCi078-B (SFC013-07-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5683. STBCi078-C (SFC013-07-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5684. STBCi079-A (SFC045-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5685. STBCi079-B (SFC045-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5686. STBCi079-C (SFC045-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5687. STBCi080-A (SFC047-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5688. STBCi080-B (SFC047-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5689. STBCi080-C (SFC047-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5690. STBCi081-A (SFC170-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5691. STBCi081-B (SFC170-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5692. STBCi081-C (SFC170-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5693. STBCi082-A (SFC888-07-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5694. STBCi082-B (SFC888-07-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5695. STBCi082-C (SFC888-07-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5696. STBCi083-A (SFC830-04-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5697. STBCi083-B (SFC830-04-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5698. STBCi084-A (SFC871-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5699. STBCi084-B (SFC871-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5700. STBCi084-C (SFC871-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5701. STBCi085-A (SFC866-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5702. STBCi085-B (SFC866-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5703. STBCi085-C (SFC866-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5704. STBCi086-A (SFC842-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5705. STBCi086-B (SFC842-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5706. STBCi087-A (SFC845-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5707. STBCi087-B (SFC845-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5708. STBCi087-C (SFC845-03-11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5709. STBCi088-A (SFC872-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5710. STBCi088-B (SFC872-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5711. STBCi088-C (SFC872-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5712. STBCi089-A (SFC868-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5713. STBCi089-B (SFC868-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5714. STBCi089-C (SFC868-03-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5715. STBCi090-A (SFC867-04-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5716. STBCi090-B (SFC867-04-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5717. STBCi091-A (SFC126-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5718. STBCi091-B (SFC126-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5719. STBCi091-C (SFC126-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5720. STBCi092-A (SFC049-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5721. STBCi092-B (SFC049-03-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5722. STBCi092-C (SFC049-03-13)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5723. STBCi093-A (SFC893-07-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5724. STBCi093-B (SFC893-07-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5725. STBCi094-A (BPC321-01-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_drug-induced liver injury

  5726. STBCi094-B (BPC321-01-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_drug-induced liver injury

  5727. STBCi094-C (BPC321-01-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_drug-induced liver injury

  5728. STBCi095-A (BPC339-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_drug-induced liver injury

  5729. STBCi096-A (BPC340-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Congenital long qt syndrome

  5730. STBCi097-A (SFC055-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5731. STBCi097-B (SFC055-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5732. STBCi097-C (SFC055-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5733. STBCi098-A (SFC048-07-14)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5734. STBCi098-B (SFC048-07-18)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5735. STBCi098-C (SFC048-07-17)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5736. STBCi099-A (SFC059-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5737. STBCi099-B (SFC059-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5738. STBCi100-A (SFC117-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5739. STBCi101-A (SFC156-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5740. STBCi102-A (SFC163-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5741. STBCi103-A (SFC294-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5742. STBCi104-A (SFC836-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5743. STBCi105-A (SFC067-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5744. STBCi106-A (SFC068-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5745. STBCi107-A (SFC104-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5746. STBCi108-A (SFC110-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5747. STBCi109-A (SFC113-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5748. STBCi110-A (SFC116-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Age-related macular degeneration

  5749. STBCi111-A (SFC131-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5750. STBCi112-A (SFC177-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5751. STBCi113-A (SFC178-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5752. STBCi114-A (SFC034-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5753. STBCi115-A (SFC162-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5754. STBCi116-A (SFC164-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5755. STBCi117-A (SFC246-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5756. STBCi118-A (SFC037-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5757. STBCi119-A (SFC044-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5758. STBCi120-A (SFC046-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5759. STBCi121-A (SFC112-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5760. STBCi122-A (SFC115-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5761. STBCi123-A (SFC053-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5762. STBCi124-A (SFC135-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5763. STBCi125-A (SFC175-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5764. STBCi126-A (SFC105-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5765. STBCi127-A (SFC107-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5766. STBCi128-A (SFC108-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5767. STBCi129-A (SFC137-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5768. STBCi130-A (SFC172-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5769. STBCi131-A (SFC295-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5770. STBCi132-A (SFC301-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5771. STBCi133-A (SFC302-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5772. STBCi134-A (SFC019-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5773. STBCi135-A (SFC033-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5774. STBCi136-A (SFC036-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5775. STBCi137-A (SFC076-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5776. STBCi138-A (SFC079-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5777. STBCi139-A (SFC101-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5778. STBCi140-A (SFC102-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5779. STBCi141-A (SFC103-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5780. STBCi142-A (SFC118-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5781. STBCi143-A (SFC122-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5782. STBCi144-A (SFC123-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5783. STBCi145-A (SFC125-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5784. STBCi146-A (SFC127-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5785. STBCi147-A (SFC128-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5786. STBCi148-A (SFC130-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5787. STBCi149-A (SFC132-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5788. STBCi150-A (SFC133-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5789. STBCi151-A (SFC145-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5790. STBCi152-A (SFC146-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5791. STBCi153-A (SFC147-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5792. STBCi154-A (SFC148-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5793. STBCi155-A (SFC149-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5794. STBCi156-A (SFC150-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5795. STBCi157-A (SFC154-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5796. STBCi158-A (SFC155-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5797. STBCi159-A (SFC158-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5798. STBCi160-A (SFC159-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5799. STBCi161-A (SFC160-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5800. STBCi162-A (SFC161-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5801. STBCi163-A (SFC165-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5802. STBCi164-A (SFC166-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5803. STBCi165-A (SFC168-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5804. STBCi166-A (SFC169-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5805. STBCi167-A (SFC174-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5806. STBCi168-A (SFC176-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5807. STBCi169-A (SFC179-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5808. STBCi170-A (SFC190-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5809. STBCi171-A (SFC191-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5810. STBCi172-A (SFC192-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5811. STBCi173-A (SFC193-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5812. STBCi174-A (SFC194-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5813. STBCi175-A (SFC195-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5814. STBCi176-A (SFC196-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5815. STBCi177-A (SFC197-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5816. STBCi178-A (SFC198-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5817. STBCi179-A (SFC243-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5818. STBCi180-A (SFC242-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5819. STBCi181-A (SFC247-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5820. STBCi182-A (SFC248-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5821. STBCi183-A (SFC250-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5822. STBCi184-A (SFC251-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5823. STBCi185-A (SFC253-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5824. STBCi186-A (SFC255-03-01 and SFC255-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5825. STBCi187-A (SFC256-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5826. STBCi188-A (SFC257-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5827. STBCi189-A (SFC258-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5828. STBCi190-A (SFC259-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5829. STBCi191-A (SFC260-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5830. STBCi192-A (SFC261-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5831. STBCi193-A (SFC262-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5832. STBCi194-A (SFC263-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5833. STBCi195-A (SFC286-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5834. STBCi196-A (SFC287-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5835. STBCi197-A (SFC288-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5836. STBCi198-A (SFC289-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5837. STBCi199-A (SFC290-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5838. STBCi200-A (SFC291-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5839. STBCi201-A (SFC292-03-02 and SFC292-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5840. STBCi202-A (SFC293-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5841. STBCi203-A (SFC296-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5842. STBCi204-A (SFC297-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5843. STBCi205-A (SFC298-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5844. STBCi206-A (SFC299-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5845. STBCi207-A (SFC300-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5846. STBCi208-A (SFC303-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5847. STBCi209-A (SFC304-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5848. STBCi210-A (SFC305-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5849. STBCi211-A (SFC306-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5850. STBCi212-A (SFC312-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5851. STBCi213-A (SFC313-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5852. STBCi214-A (SFC314-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5853. STBCi215-A (SFC318-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5854. STBCi216-A (SFC319-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5855. STBCi217-A (SFC320-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5856. STBCi218-A (SFC357-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5857. STBCi219-A (SFC358-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5858. STBCi220-A (SFC359-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5859. STBCi221-A (SFC360-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5860. STBCi222-A (SFC361-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5861. STBCi223-A (SFC363-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5862. STBCi224-A (SFC364-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5863. STBCi225-A (SFC365-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5864. STBCi226-A (SFC366-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5865. STBCi227-A (SFC367-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5866. STBCi228-A (SFC368-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5867. STBCi229-A (SFC369-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5868. STBCi230-A (SFC372-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5869. STBCi231-A (SFC374-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5870. STBCi232-A (SFC375-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5871. STBCi233-A (SFC873-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5872. STBCi234-A (SFC874-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5873. STBCi235-A (SFC879-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5874. STBCi236-A (SFC880-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5875. STBCi237-A (SFC881-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5876. STBCi238-A (SFC882-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5877. STBCi239-A (SFC883-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5878. STBCi240-A (SFC884-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5879. STBCi241-A (SFC885-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5880. STBCi242-A (SFC886-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5881. STBCi243-A (SFC991-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5882. STBCi244-A (SFC993-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5883. STBCi245-A (SFC994-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5884. STBCi246-A (SFC995-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5885. STBCi247-A (SFC996-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5886. STBCi248-A (SFC999-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5887. STBCi249-A (SFC171-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5888. STBCi250-A (SFC997-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5889. STBCi251-A (SFC998-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5890. STBCi252-A (SFC254-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5891. STBCi253-A (SFC184-01-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5892. STBCi254-A (SFC143-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5893. STBCi255-A (SFC183-01-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5894. STBCi256-A (SFC144-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5895. STBCi257-A (SFC185-01-11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5896. STBCi258-A (SFC090-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5897. STBCi259-A (SFC032-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5898. STBCi260-A (SFC279-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5899. STBCi261-A (SFC186-01-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5900. STBCi262-A (SFC271-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5901. STBCi263-A (SFC268-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5902. STBCi264-A (SFC142-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5903. STBCi265-A (SFC121-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5904. STBCi266-A (SFC072-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5905. STBCi267-A (SFC027-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5906. STBCi268-A (SFC077-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5907. STBCi269-A (BPC943-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5908. STBCi270-A (BPC944-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5909. STBCi271-A (BPC936-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5910. STBCi272-A (BPC930-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5911. STBCi273-A (BPC928-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5912. STBCi274-A (BPC935-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5913. STBCi275-A (BPC937-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5914. STBCi276-A (BPC933-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5915. STBCi277-A (BPC934-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5916. STBCi278-A (SFC245-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5917. STBCi279-A (SFC063-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5918. STBCi280-A (SFC066-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5919. STBCi281-A (SFC167-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5920. STBCi282-A (SFC138-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5921. STBCi283-A (SFC073-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5922. STBCi284-A (BPC939-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5923. STBCi285-A (BPC940-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5924. STBCi286-A (BPC929-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5925. STBCi287-A (BPC946-04-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5926. STBCi288-A (SFC028-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5927. STBCi289-A (SFC030-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5928. STBCi290-A (SFC069-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5929. STBCi291-A (SFC080-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5930. STBCi292-A (SFC139-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5931. STBCi293-A (SFC843-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5932. STBCi294-A (SFC844-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5933. STBCi295-A (SFC847-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5934. STBCi295-B (SFC847-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5935. STBCi296-A (SFC864-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5936. STBCi297-A (SFC061-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5937. STBCi298-A (SFC865-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5938. STBCi299-A (BPC931-01-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5939. STBCi300-A (BPC932-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5940. STBCi301-A (BPC949-04-11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5941. STBCi302-A (BPC945-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5942. STBCi303-A (SFC071-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5943. STBCi304-A (SFC074-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5944. STBCi305-A (SFC083-03-10 and SFC083-07-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5945. STBCi306-A (SFC087-03-04 and SFC087-07-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5946. STBCi307-A (SFC088-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5947. STBCi308-A (SFC249-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5948. STBCi309-A (SFC391-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5949. STBCi310-A (SFC846-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5950. STBCi311-A (BPC941-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5951. STBCi312-A (BPC333-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5952. STBCi313-A (BPC334-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5953. STBCi314-A (BPC335-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5954. STBCi315-A (BPC336-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5955. STBCi316-A (SFC244-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5956. STBCi317-A (SFC241-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5957. STBCi318-A (SFC200-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5958. STBCi319-A (SFC199-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  5959. STBCi320-A (SFC031-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5960. STBCi324-A (SFC826-04-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5961. STJUDEi004-A (INS3)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  5962. STJUDEi004-A-1 (INS3 Isogenic)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  5963. STJUDEi005-A (INS14)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  5964. STJUDEi005-A-1 (INS14 Isogenic)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  5965. STJUDEi007-A (PCS201)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Normal (average)

  5966. STJUDEi007-A-1 (2A5)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Samd9-associated hereditary myelodysplastic syndrome

  5967. STJUDEi007-A-2 (4H6)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Samd9-associated hereditary myelodysplastic syndrome

  5968. STJUDEi007-A-3 (3G10)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Samd9-associated hereditary myelodysplastic syndrome

  5969. STJUDEi007-A-4 (5B9)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Samd9-associated hereditary myelodysplastic syndrome

  5970. SUHi001-A (RES143 and Cell line 1 143)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5971. SUHi002-A (RES145 and Cell line 2 145)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5972. SUHi003-A (RES146 and Cell line 3 146)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5973. SUHi004-A (RES152 and cell line4 152)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Gastritis

  5974. SUHi005-A (RES165 and Cell line5 165)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5975. SUHi006-A (RES169 and Cell line6 169)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5976. SUHi007-A (RES102 and Cell line 7 102:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5977. SUHi008-A (Cell line 8 104:5 and RES104)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Asthma

  5978. SUHi009-A (RES105 and Cell line 12 105:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5979. SUHi010-A (RES117 and Cell line 9 117:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5980. SUHi011-A (RES151 and Cell line 13 151)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Asthma

  5981. SUHi012-A (RES163 and Cell line 14 163)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5982. SUHi013-A (RES110 and Cell line 11 110:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5983. SUHi014-A (RES120 and Cell line 10 120:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Aortic dilatation

  5984. SUHi015-A (RES141 and Cell line 15 141)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5985. SUHi016-A (RES142 and Cell line 16 142:3)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5986. SUHi017-A (RES158 and Cell line 24 158)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Breast carcinoma

  5987. SUHi018-A (RES168 and Cell line 17 168)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Hypertension

  5988. SUHi020-A (RES114 and Cell line 19 114:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5989. SUHi021-A (RES116 and Cell line 20 116:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5990. SUHi022-A (RES118 and Cell line 21 118:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5991. SUHi023-A (RES121 and Cell line 22 121:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

    Disease:

    Type 2 diabetes mellitus

  5992. SUHi024-A (RES174 and Cell line 23 174)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5993. SUSMi001-A (RY3)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Pelizaeus-merzbacher disease

  5994. SUSMi001-A-1 (128Lp1)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Pelizaeus-merzbacher disease

  5995. UCSFi001-A-64 (P633L RBM20 iPSCs)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_dilated cardiomyopathy

  5996. UCSFi001-A-65

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_dilated cardiomyopathy

  5997. SUSMi002-A (02-005)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Pelizaeus-merzbacher disease

  5998. SUSMi003-A (0524-1)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Normal (average)

  5999. SUSMi005-A

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  6000. SUSMi005-A-1 (SNCA3X 0KO C1 and SNCA3X 0KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  6001. SUSMi005-A-2 (SNCA3X 1KO C2 and SNCA3X 1KO C1)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  6002. SUSMi005-A-3 (SNCA3X 2KO C1 and SNCA3X 2KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  6003. SUSMi005-A-4 (SNCA3X 3KO C1 and SNCA3X 3KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  6004. SUSMi005-A-5 (SNCA3X 4KO C1 and SNCA3X 4KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  6005. SUTCMi001-A

    China Shandong University of Traditional Chinese Medicine (SUTCM)
    Disease:

    Normal (average)

  6006. SXMUi001-A (SXMUi002-A-1 and HB-iPSCs)

    China Shanxi Medical University (SXMU)
    Disease:

    Hemophilia b

  6007. SXMUi002-A (SXMUi001-A-1 and F8-iPSC)

    China Shanxi Medical University (SXMU)
    Disease:

    Hemophilia a

  6008. SYSUi002-A (CSFPhiPSC01.1)

    China Sun Yat-sen University (SYSU)
    Disease:

    Coronary slow flow phenomenon

  6009. SYSUi005-A

    China Sun Yat-sen University (SYSU)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  6010. SYSUi007-A

    China Sun Yat-sen University (SYSU)
    Disease:

    Aicardi-goutieres syndrome

  6011. SYSUSCi001-A (CC-hiPSCs)

    China Sun Yat-Sen University, center for stem cell biology and tissue engineering (SYSUSC)
    Disease:

    Congenital cataract

  6012. SYSUSCi002-A (FNAIT-hiPSCs)

    China Sun Yat-Sen University, center for stem cell biology and tissue engineering (SYSUSC)
    Disease:

    Fetal and neonatal alloimmune thrombocytopenia

  6013. SYSUSCi004-A (IMO-hiPSCs)

    China Sun Yat-Sen University, center for stem cell biology and tissue engineering (SYSUSC)
    Disease:

    Autosomal recessive malignant osteopetrosis

  6014. SYSUTFi001-A

    China The First Affiliated Hospital (SYSUTF)
    Disease:

    Hepatocellular carcinoma

  6015. SZBKi001-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  6016. SZBKi001-B

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  6017. SZBKi002-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  6018. SZBKi002-B

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  6019. SZBKi003-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  6020. SZBKi004-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  6021. SZBKi005-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  6022. SZBKi006-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  6023. SZBKi006-B

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  6024. SZGJMSi001-A (ZLP-2)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Schizophrenia

  6025. SZGJMSi002-A (TSQ-1)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Obsessive-compulsive disorder

  6026. SZGJMSi003-A (TSH-2)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Normal (average)

  6027. SZGJMSi004-A (WJM-1)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Depression

  6028. TAUi001-A (UTA.09703.HCMJp)

    Finland Tampere University (TAU)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  6029. TAUi001-A-1 (JPH2)

    Finland Tampere University (TAU)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  6030. TAUi002-A (UTA.04602.WT)

    Finland Tampere University (TAU)
    Disease:

    Normal (average)

  6031. TAUi003-A (UTA.11505.WTsb)

    Finland Tampere University (TAU)
    Disease:

    Normal (average)

  6032. TAUi004-A (UTA.05208.CPVT)

    Finland Tampere University (TAU)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  6033. TAUi005-A (UTA.14511.CPVT)

    Finland Tampere University (TAU)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  6034. TAUi006-A (UTA.00102.LQT1)

    Finland Tampere University (TAU)
    Disease:

    Long qt syndrome 1

  6035. TAUi006-B (UTA.00118.LQT1)

    Finland Tampere University (TAU)
    Disease:

    Long qt syndrome 1

  6036. TAUi007-A (UTA.00208.LQT1)

    Finland Tampere University (TAU)
    Disease:

    Long qt syndrome 1

  6037. TAUi007-B (UTA.00211.LQT1)

    Finland Tampere University (TAU)
    Disease:

    Long qt syndrome 1

  6038. TAUi008-A (TAU2106C1.MS)

    Finland Tampere University (TAU)
    Disease:

    Multiple sclerosis

  6039. TCGINKi001-A (INK-iSCA12-001_(SC-003))

    India CHINTA (TCGINK)
    Disease:

    Spinocerebellar ataxia type 12

  6040. TCGINKi002-A (INK-iCON-003)

    India CHINTA (TCGINK)
    Disease:

    Normal (average)

  6041. TCGINKi003-A (INK-iCON-004)

    India CHINTA (TCGINK)
    Disease:

    Normal (average)

  6042. TCGINKi004-A (INK-iSCA12-002)

    India CHINTA (TCGINK)
    Disease:

    Spinocerebellar ataxia type 12

  6043. TCIERi001-A (IER-EK1)

    Taiwan Institute of Eye Research, Hualien Tzu Chi Hospital (TCIER)
    Disease:

    Normal (average)

  6044. TIGETi001-A (ND1.2)

    Italy San Raffaele Telethon Institute for Gene Therapy (SR-Tiget) (TIGET)
    Disease:

    Normal (average)

  6045. TIGETi003-A (GLD1.3)

    Italy San Raffaele Telethon Institute for Gene Therapy (SR-Tiget) (TIGET)
    Disease:

    Krabbe disease

  6046. TISSUi001-A (HUMIMIC101, StemUse101 and SU101)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  6047. TISSUi002-A (HUMIMIC102, StemUse102, SU102)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  6048. TISSUi003-A (HUMIMIC103, StemUse103, SU103)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  6049. TISSUi005-A (HUMIMIC105, StemUse105, SU105)

    Germany TissUse GmbH (TISSU)
    Disease:

    Leukemia

  6050. TISSUi006-A (HUMIMIC106, StemUse106 and SU106)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  6051. TISSUi007-A (HUMIMIC107, StemUse107 and SU107)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  6052. TMOi001-A (Gibco Episomal iPSC Line; A18945)

    United States Thermo Fisher Scientific (TMO)
    Disease:

    Normal (average)

  6053. TMPi001-A (K001 i6 and KO-001 i6)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6054. TMPi001-B (K001 i9, KO-001 i9, K001 c9 and KO-001 c9)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6055. TMPi002-A (K003 c14, K003 a14, KO-003 a14 and KO-003 c14)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6056. TMPi002-B (KO-003 a20, KO-003 c20, K003 c20 and K003 a20)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6057. TMPi003-A (KO-005 z12, K005 z12, KO-005 c12 and K005 c12)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6058. TMPi003-B (K005 z13, KO-005 c13, K005 c13 and KO-005 z13)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6059. TMPi004-A (K008 c13, KO-008 c13, K008 i13 and KO-008 i13)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6060. TMPi004-B (K008 c44, KO-008 c44, K008 i44 and KO-008 i44)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6061. TMPi005-A (K011 c6 and KO-011 c6)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6062. TMPi005-B (K011 c10 and KO-011 c10)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6063. TMPi006-A (MR-001 x3, MR001 x3, MR-001 c3 and MR001 c3)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6064. TMPi006-B (MR001 x15, MR-001 x15, MR-001 c15 and MR001 c15)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6065. TMPi007-A (MR-010 c3 and MR010 c3)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6066. TMPi007-B (MR-010 c18 and MR010 c18)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6067. TMPi008-A (MR-013 c3 and MR013 c3)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6068. TMPi008-B (MR-013 c13 and MR013 c13)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6069. TMPi009-A (MR014 c12.1.1, MR-014 c12, MR-014 c12.1.1 and MR014 c12)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6070. TMPi009-B (MR014 c27 and MR-014 c27)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6071. TMPi010-A (K013 c20 and KO-013 c20)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6072. TMPi010-B (K013 c39 and KO-013 c39)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6073. TMPi011-A (K015 c1 and KO-015 c1)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6074. TMPi011-B (K015 c9 and KO-015 c9)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  6075. TMPi012-A (MR-023 c17 and MR023 c17)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6076. TMPi012-B (MR023 c22 and MR-023 c22)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6077. TMPi013-A (MR-012 and MR012)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6078. TMPi013-B (MR-012 c12 and MR012 c12)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6079. TMPi014-A (MR030 c1 and MR-030 c1)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6080. TMPi014-B (MR030 c2 and MR-030 c2)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6081. TMPi015-A (NR-002 c2 and NR002 c2)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6082. TMPi015-B (NR002 c21 and NR-002 c21)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6083. TMPi016-A (NR003 c6 and NR-003 c6)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6084. TMPi016-B (NR003 c9 and NR-003 c9)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  6085. TNRMCi001-A (iTAF32)

    Russia Tomsk National Research Medical Center of the Russian Academy of Sciences (TNRMC)
    Disease:

    Cystic fibrosis

  6086. TONGJIi001-A (ZS15)

    China Tongji University (TONGJI)
    Disease:

    Infertility

  6087. TRDSi001-A (TRDS-Cardio-021)

    Israel Technion Research and Development Foundation (TRDS)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  6088. TRDSi002-A

    Israel Technion Research and Development Foundation (TRDS)
    Disease:

    Normal (average)

  6089. TRDSi002-A-1 (TRDS-Cardio-ArcLight)

    Israel Technion Research and Development Foundation (TRDS)
    Disease:

    Normal (average)

  6090. TRDSi004-A (TRDS-Cardio-012)

    Israel Technion Research and Development Foundation (TRDS)
    Disease:

    Long qt syndrome 2

  6091. TRNDi032-A (HT977A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Alagille syndrome

  6092. TRNDi033-A (HT1001-B)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Normal (average)

  6093. TRNDi034-A (HT1002-A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Normal (average)

  6094. TRNDi035-A (HT1004-B)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Normal (average)

  6095. TRNDi036-A (HT980A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Alagille syndrome

  6096. TRNDi037-A (HT976A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Alagille syndrome

  6097. TRNDi038-A (HT978A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Alagille syndrome

  6098. TRNDi042-A (HT528A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Mucopolysaccharidosis type iiib

  6099. TUMi001-A (C25)

    Germany Technische Universität München (TUM)
    Disease:

    Normal (average)

  6100. TUSMi001-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Normal (average)

  6101. TUSMi002-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Normal (average)

  6102. TUSMi003-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  6103. TUSMi004-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsessive-compulsive disorder

  6104. TUSMi005-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsolete_bipolar disorder

  6105. TUSMi006-A (15M0014)

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsolete_alzheimer's disease

  6106. TUSMi007-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  6107. TUSMi008-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  6108. TUSMi012-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Glioma

  6109. TUSMi013-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Parkinson disease

  6110. TUSMi014-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Parkinson disease

  6111. TYWHSTi002-A

    China Tianyou Hospital, Wuhan University of Science and Technology (TYWHST)
    Disease:

    Pendred syndrome

  6112. UAEUi001-A

    United Arab Emirates United Arab Emirates University (UAEU)
    Disease:

    Ventricular septal defect

  6113. UALGi003-A (BUB1P2-iPSC Cl1)

    Portugal Universidade do Algarve (UALG)

  6114. UALGi003-B (BUB1P2-iPSC Cl2)

    Portugal Universidade do Algarve (UALG)

  6115. UAMi001-A (PCCA23-FiPS4F8)

    Spain Universidad Autonoma de Madrid (UAM)
    Disease:

    Propionic acidemia

  6116. UAMi005-A

    Spain Universidad Autonoma de Madrid (UAM)
    Disease:

    Nonketotic hyperglycinemia

  6117. UAZTi009-A (MKAZ1)

    United States University of Arizona (UAZT)
    Disease:

    Normal (average)

  6118. UAZTi011-A (MKAZ3)

    United States University of Arizona (UAZT)
    Disease:

    Pontocerebellar hypoplasia type 1b

  6119. UBi001-A

    Spain University of Barcelona (UB)
    Disease:

    Normal (average)

  6120. UBi001-A-1

    Spain University of Barcelona (UB)
    Disease:

    Sanfilippo syndrome type c

  6121. UBi001-A-2

    Spain University of Barcelona (UB)
    Disease:

    Sanfilippo syndrome type c

  6122. UBi005-A (BJ_iPSC_SV4F_9)

    Spain University of Barcelona (UB)
    Disease:

    Normal (average)

  6123. UBCi002-A

    Canada University of British Columbia (UBC)
    Disease:

    Leukodystrophy, hypomyelinating, 22

  6124. UBGi001-A

    China uBriGene (Suzhou) Biosciences Co., Ltd. (UBG)
    Disease:

    Normal (average)

  6125. UBTi001-A (PEB-AL#6)

    Austria Medical University of Graz (UBT)
    Disease:

    Normal (average)

  6126. UBTi001-A-1 (PEB-AL#6CD43Rep#3)

    Austria Medical University of Graz (UBT)
    Disease:

    Normal (average)

  6127. UBTi002-A (PEB-HM1 #3)

    Austria Medical University of Graz (UBT)
    Disease:

    Normal (average)

  6128. UBTi002-B (PEB-HM1 #5)

    Austria Medical University of Graz (UBT)
    Disease:

    Normal (average)

  6129. UBTi002-C (PEB-HM1 #8)

    Austria Medical University of Graz (UBT)
    Disease:

    Normal (average)

  6130. UCLi001-A (HHItC9S-V19)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  6131. UCLi002-A (HHItC9D-V34 and DN19)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  6132. UCLi003-A (TSM(exon10+16)V97)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  6133. UCLi004-A (RCi173 and RCFB60c6)

    United Kingdom University College London (UCL)
    Disease:

    Amyotrophic lateral sclerosis

    Disease:

    Frontotemporal dementia

  6134. UCLi004-B (RCFB60c7 and RCi177)

    United Kingdom University College London (UCL)
    Disease:

    Amyotrophic lateral sclerosis

    Disease:

    Frontotemporal dementia

  6135. UCLi004-C (RCi172 and RCFB60c2)

    United Kingdom University College London (UCL)
    Disease:

    Amyotrophic lateral sclerosis

    Disease:

    Frontotemporal dementia

  6136. UCLi005-A (LGMD2D Pt. 4 and LGMD2D #4)

    United Kingdom University College London (UCL)
    Disease:

    Limb-girdle muscular dystrophy

  6137. UCLi006-A (LCMD-L302P-UCL01C2)

    United Kingdom University College London (UCL)
    Disease:

    Congenital muscular dystrophy due to lmna mutation

  6138. UCLi009-A (CB1D)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  6139. UCLi009-B (CB1E)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  6140. UCLi010-A

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  6141. UCLi010-B (GL1B)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  6142. UCLi011-A

    United Kingdom University College London (UCL)
    Disease:

    Duchenne muscular dystrophy

  6143. UCLi012-A

    United Kingdom University College London (UCL)
    Disease:

    Duchenne muscular dystrophy

  6144. UCLi021-A (CLN5c.335G>A;619T>C and 484Pb)

    United Kingdom University College London (UCL)
    Disease:

    Cln5

  6145. UCLi022-A (546Pa and CLN5c.1072-1073delTT)

    United Kingdom University College London (UCL)
    Disease:

    Cln5

  6146. UCLi024-A (SMID277 and GOS111B)

    United Kingdom University College London (UCL)
    Disease:

    Argininosuccinic aciduria

  6147. UCLi026-A (UCL-NG-ADCY5-001)

    United Kingdom University College London (UCL)
    Disease:

    Dyskinesia with orofacial involvement, autosomal dominant

  6148. UCONNi001-A (LL237)

    United States University of Connecticut (UCONN)
    Disease:

    Charge syndrome

  6149. UCSCi001-A (SII-1802)

    Italy Università Cattolica del Sacro Cuore- Fondazione Policlinico Universitario "A. Gemelli" IRCCS (UCSC)
    Disease:

    Amyotrophic lateral sclerosis

  6150. UCSCi002-A (LIF-1989)

    Italy Università Cattolica del Sacro Cuore- Fondazione Policlinico Universitario "A. Gemelli" IRCCS (UCSC)
    Disease:

    Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia

  6151. UCSDi001-A (UCSD182i-3-2 and iPSCORE_3_2)

    United States University of California,San Diego (UCSD)
    Disease:

    Normal (average)

  6152. UCSDi001-A-1 (UCSD242i-LQT1-1 and LQT1_2_5_iPSC_P17)

    United States University of California,San Diego (UCSD)
    Disease:

    Long qt syndrome 1

  6153. UCSDi001-A-2 (LQT3_35_iPSC_P15 and UCSD243i-LQT3-1)

    United States University of California,San Diego (UCSD)
    Disease:

    Long qt syndrome 3

  6154. UCSDi001-A-3 (LQT3_4_28_Homo_52_iPSC_P15 and UCSD244i-LQT3-2)

    United States University of California,San Diego (UCSD)
    Disease:

    Long qt syndrome 3

  6155. UCSDi001-A-4 (UCSD245i-CNTL-1 and T036_SNP1_Het_1_iPSC_P15_R01)

    United States University of California,San Diego (UCSD)
    Disease:

    Long qt syndrome 1

  6156. UCSDi001-A-5 (UCSD246i-CNTL-2 and T036_SNP1_Het_3_iPSC_P16_R01)

    United States University of California,San Diego (UCSD)
    Disease:

    Long qt syndrome 3

  6157. UCSFi001-A (wtc11, Wtc11, WTC, WTC11 and GM25256)

    United States Conklin Lab, Gladstone/UCSF (UCSF)
    Disease:

    Normal (average)

  6158. UCSFi002-A (BAG3-P209L)

    United States Conklin Lab, Gladstone/UCSF (UCSF)

  6159. UEFi004-A

    Finland University of Eastern Finland (UEF)
    Disease:

    Cstb wt allele

  6160. UEFi005-A (CO1)

    Finland University of Eastern Finland (UEF)
    Disease:

    Normal (average)

  6161. UEFi006-A (CO2)

    Finland University of Eastern Finland (UEF)
    Disease:

    Normal (average)

  6162. UEFi007-A (CO3)

    Finland University of Eastern Finland (UEF)
    Disease:

    Normal (average)

  6163. UEFi008-A (FTD1)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  6164. UEFi009-A (FTD2)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  6165. UEFi010-A (FTD3)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  6166. UEFi011-A (FTD4)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  6167. UEFi012-A (FTD5)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  6168. UEFi013-A (FTD6)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  6169. UGENTi001-A (UGENT-MFS003)

    Belgium Ghent University (UGENT)
    Disease:

    Marfan syndrome

  6170. UGENTi001-A-1 (UGENT-MFS003-CRISPR)

    Belgium Ghent University (UGENT)
    Disease:

    Marfan syndrome

  6171. UGENTi002-A

    Belgium Ghent University (UGENT)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  6172. UGENTi002-A-1

    Belgium Ghent University (UGENT)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  6173. UGENTi003-A (Clone_1 and EMC379i/c1)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  6174. UGENTi003-B (EMC379i/c3 and Clone_3)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  6175. UGENTi003-C (EMC379i/c4 and Clone_4)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  6176. UGENTi004-A (Clone_1 and EMC380i/c1)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  6177. UGENTi004-B (Clone_6 and EMC380i/c6)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  6178. UGENTi004-C (Clone_7 and EMC380i/c7)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  6179. UGENTi005-A (EMC368i/c1)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  6180. UGENTi005-B (EMC368i/c2)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  6181. UGENTi005-C (EMC368i/c6)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  6182. UGENTi006-A (EMC369i/c3)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  6183. UGENTi006-B (EMC369i/c8)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  6184. UGENTi006-C (EMC369i/c9)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  6185. UGENTi007-A (EMC370i/c4)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  6186. UGENTi007-B (EMC370i/c6)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  6187. UGENTi007-C (EMC370i/c14)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  6188. UGOTSAi002-B (N1-001iC2)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  6189. UGOTSAi003-A (N1-002iC3A)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  6190. UGOTSAi003-B (N1-002iC4)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  6191. UGOTSAi004-A (N1-003iC3)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  6192. UGOTSAi004-B (N1-003iC4)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  6193. UGOTSAi005-A (N1-004iC2)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Normal (average)

  6194. UGOTSAi005-B (N1-004iC6)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Normal (average)

  6195. UGOTSAi006-A (N1-005iC1)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  6196. UHi002-A (HEL13.1 and ALS50)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  6197. UHi003-A (ALS75 and HEL15.14)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  6198. UHi004-A (HEL157.1)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  6199. UHi004-B (HEL157.3)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  6200. UHi005-A (HEL158.1)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  6201. UHi005-B (HEL158.2)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  6202. UHi006-A (HEL24.3)

    Finland University of Helsinki (UH)
    Disease:

    Normal (average)

  6203. UHi006-A-1 (UHi001-A, HEL24.3-SOX2-nTdT-C9-H5 and HEL24.3-SOX2-nTdT)

    Finland University of Helsinki (UH)
    Disease:

    Normal (average)

  6204. UHi006-A-2 (HEL24.3-OCT4-nEmGFP-A-G3, UHi001-B and HEL24.3-OCT4-nEmGFP)

    Finland University of Helsinki (UH)
    Disease:

    Normal (average)

  6205. UHi006-A-3 (HEL24.3_IFIH1KO)

    Finland University of Helsinki (UH)
    Disease:

    Type i diabetes mellitus

  6206. UHi007-A (HEL47.2)

    Finland University of Helsinki (UH)
    Disease:

    Normal (average)

  6207. UHOMi001-A (iPCD02.30)

    France University Hospital of Montpellier (UHOM)
    Disease:

    Primary ciliary dyskinesia

  6208. UHOMi007-A (SMOK1)

    France University Hospital of Montpellier (UHOM)
    Disease:

    Normal (average)

  6209. UIOi001-A (AG27)

    Norway University of Oslo (UIO)
    Disease:

    Normal (average)

  6210. UIOi002-A (iPSC APOE3/3: Unaffected (Coriell #AG09173, female, Age 75))

    United States University of Oslo (UIO)

  6211. UIOi006-A (iPSC APOE4/4: Sporadic AD (Coriell #AG10788, female, Age 87))

    Norway University of Oslo (UIO)

  6212. UJNi001-A

    China University of Jinan (UJN)
    Disease:

    Cornelia de lange syndrome

  6213. UJSi001-A

    China Jiangsu University (UJS)
    Disease:

    Schizophrenia

  6214. UJSi003-A

    China Jiangsu University (UJS)
    Disease:

    Hereditary spastic paraplegia

  6215. UJSi004-A

    China Jiangsu University (UJS)
    Disease:

    Schizophrenia

  6216. UJSi005-A

    China Jiangsu University (UJS)
    Disease:

    Schizophrenia

  6217. UJSi006-A

    China Jiangsu University (UJS)
    Disease:

    Schizophrenia

  6218. UKAi001-A (iPS1 and hsc3_hiPS_11)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6219. UKAi001-A-1 (hsc3_hiPS_11_4 and IRF8-/- iPS1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6220. UKAi001-B (iPS2 and hsc3_hiPS_29)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6221. UKAi001-B-1 (hsc3_hiPS_29_23 and IRF8-/- iPS2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6222. UKAi001-C (hsc3_hiPS_40 and iPS3)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6223. UKAi001-C-1 (hsc3_hiPS_40_16_6 and IRF8-/- iPS3)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6224. UKAi002-A (PBMNC2_hiPS_007 and PV1 JAK2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  6225. UKAi002-A-1 (PV1 JAK2 : CXCL4 KO)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  6226. UKAi002-B (PBMNC2_hiPS_009 and PV1 JAK2 V617F het)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  6227. UKAi002-B-1 (PV1 JAK2 V617F het : CXCL4 KO)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  6228. UKAi003-A (hsc4_hiPS_021 and PV2 JAK2 V617F hom)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  6229. UKAi003-A-1 (PV2 JAK2 V617F het)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  6230. UKAi003-A-2 (PV2 JAK2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  6231. UKAi004-A (P4_wt4 and patient 1 control 1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6232. UKAi004-B (patient 1 control 2 and P4_wt8)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6233. UKAi004-C (P4_mut13 and patient 1 D816V 1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6234. UKAi004-D (P4_mut28 and patient 1 D816V 2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6235. UKAi004-E (P4_mut30 and patient 1 D816V 3)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6236. UKAi007-A (P13_wt5 and Patient 2 control 1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6237. UKAi007-B (P13_mut1 and Patient 2 D816V 1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6238. UKAi008-A (Patient 3 control 1 and P15_wt37)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6239. UKAi008-B (Patient 3 control 2 and P15_wt108)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6240. UKAi008-C (Patient 3 D816V 1 and P15_mut131)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  6241. UKAi009-A (BM 102-2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Normal (average)

  6242. UKAi010-A (BM 104-12)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Normal (average)

  6243. UKAi011-A (BM 106-3)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Normal (average)

  6244. UKBi001-B

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Machado-joseph disease

  6245. UKBi002-A (iLB-C2-36m-r2)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6246. UCSFi002-A-1

    Germany Universitätsklinikum Bonn (UKB)

  6247. UKBi003-A (iLB-MJD1-32m-r9 and LB-32-r9)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Machado-joseph disease

  6248. UKBi004-A (LB-30-12 and iLB-C1-30m-r12)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6249. UKBi005-A (iLB-C-31f-r1 and LB-31-1)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6250. UKBi006-A (iLB-C-35m-r1 and LB-35-1)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6251. UKBi007-A (LB-33-5 and iLB-MJD3-33f-r5)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Machado-joseph disease

  6252. UKBi008-A (iLB-MJD4-34m-r1 and LB-34-1)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Machado-joseph disease

  6253. UKBi010-A (iLB-DS-95f-r8)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Dravet syndrome

  6254. UKBi011-A (iLB-AD-169bm-s24)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Alzheimer disease

  6255. UKBi012-A (iLB-C-108bf-s3)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6256. UKBi013-A (iLB-C-133bm-s4)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6257. UKBi014-A (A-257s2)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Walker-warburg syndrome

  6258. UKBi015-A (iLB-C16bm-s6)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6259. UKBi015-A-6 (iLB-C16bm-s6 edit BAG3 E2)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  6260. UKBi015-A-7 (iLB-C16bm-s6 edit BAG3 E10)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  6261. UKBi015-A-8 (iLB-C16bm-s6 non-edit BAG3 E5)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  6262. UKBi015-B (iLB-C16bm-s16)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6263. UKBi015-B-1 (iLB-C16bm-s16 edit DNMT3A KO E11)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Clonal hematopoiesis of indeterminate potential

  6264. UKBi015-B-2 (iLB-C16bm-s16 edit EMILIN1 C1606T E9)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Aortic root aneurysm

  6265. UKBi015-B-3 (iLB-C16bm-s16 edit TET2 KO E1)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Clonal hematopoiesis of indeterminate potential

  6266. UKBi015-B-4 (iLB-C16bm-s16 edit MUC4 KO E8)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Bicuspid aortic valve

  6267. UKBi015-B-5 (iLB-C16bm-s16 edit AAVS1-doxCx43-E11 Hom)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6268. UKBi015-B-6 (iLB-C16bm-s16 edit AAVS1-dox-rEstus(ASAP-GTA)-E5 Hom)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6269. UKBi016-A (iLB-C107bm-s9)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6270. UKBi017-A (iLB-C14m-s11)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6271. UKBi018-A (iLB-C-106bf-s8)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6272. UKBi019-A (iLB-C89bf-s7)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6273. UKBi020-A (iLB-C-105bm-s4)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6274. UKBi021-A (iLB-C-109bm-s6)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  6275. UKBi022-A (iLB-BAG3-301bm-s2)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  6276. UKBi022-A-1 (iLB-BAG3-301bm-s2 BAG3 edit)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  6277. UKBi023-A (iLB-BAG3-P209L-313bm-s9)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  6278. UKBi023-A-1 (iLB-BAG3-P209L-313bm-s9 BAG3 edit)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  6279. UKEi001-A (ERC001sv1162)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  6280. UKEi001-A-1 (CRYABhom)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Desminopathy

  6281. UKEi001-A-2 (Biallelic NRAP-KO)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Cardiomyopathy

  6282. UKEi001-A-3 (NRAP-OE)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Cardiomyopathy

  6283. UCSFi001-A-1T (PRKD1-G592R-het)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Congenital heart disease

  6284. UCSFi001-A-1U (PRKD1-G592R-hom)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Congenital heart disease

  6285. UKEi001-B (ERC001sv1352)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  6286. UKEi001-C (ERC001sv1355)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  6287. UKEi002-A (ERC017sv2575)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  6288. UKEi002-B (ERC017sv2576)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  6289. UKEi002-C (ERC017sv2596)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  6290. UKEi003-A (ERC018sv1583)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  6291. UKEi003-B (ERC018sv1590)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  6292. UKEi003-C (ERC018sv1634)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  6293. UKEi070-A (Het)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  6294. UKEi070-A-1 (Rep 28 and Iso Co)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  6295. UKEi070-A-2 (Bi-allelic mutant and Mut 103)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  6296. UKERi001-A (UKERiG3G-R1-047)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6297. TMOi001-A-4 (SPG11_HA)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6298. UKERi002-A (UKERiM89-R1-006)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Obsolete_parkinson's disease

  6299. UKERi003-A (UKERiPX7-R1-001)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Obsolete_parkinson's disease

  6300. UKERi004-A (UKERi88H-R1-001)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Obsolete_parkinson's disease

  6301. UKERi005-A (UKERiO3H-R1-001)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6302. UKERi006-A (UKERi82A-R1-002)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6303. UKERi006-B (UKERi82A-S1-017)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6304. UKERi009-A (UKERi33Q-R2-006)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6305. UKERi010-A (UKERi7MN-S1-010)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6306. UKERi010-A-1 (UKERi7MN-010-1)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6307. UKERi010-A-2 (UKERi7MN-010-2)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6308. UKERi011-A

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Focal segmental glomerulosclerosis

  6309. UKHGi001-A (M-PKE (c))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Normal (average)

  6310. DPEDi001-A-1

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Atrial fibrillation

  6311. UKHGi001-B (M-PKE (e))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Normal (average)

  6312. UKHGi002-A (F-PKE (2))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Normal (average)

  6313. UKHGi002-B (F-PKE (3))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Normal (average)

  6314. UKHGi003-A (PKE (C))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Obsolete_autism spectrum disorder

    Disease:

    Intellectual disability

  6315. UKHGi003-B (PKE (D))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Obsolete_autism spectrum disorder

    Disease:

    Intellectual disability

  6316. MRIi016-A-1 (SHOX2 c.*28T>C_isoWT)

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Atrial fibrillation

  6317. MRIi016-A-2

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Atrial fibrillation

  6318. UKJi001-A (PKP2-hiPSC)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Normal (average)

  6319. UKJi003-A (hiPSC-FD)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Fabry disease

  6320. UKJi004-A (hiPSC-WT)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Normal (average)

  6321. UKJi005-A (hiPSC-FS.2)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Normal (average)

  6322. UKJi006-A (PKP2-hiPSC-ARVC)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  6323. UKKi006-A (D4-cB, M4C4 and NP0053-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6324. UKKi007-A (NP0014-6 and UKK007Ai)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  6325. UKKi007-B (NP0014-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  6326. UKKi008-A (NP0016-3)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6327. UKKi009-A (NP0011-8)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6328. UKKi009-B (NP0011-19)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6329. UKKi011-A (NP0040-8)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6330. UKKi012-A (NP0041-17 and NP0041)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6331. UKKi016-A (NP0078-10)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6332. UKKi016-B (NP0078-12)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6333. UKKi016-C (NP0078-13)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6334. UKKi017-A (NP0075-8D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6335. UKKi017-B (NP0075-10K)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6336. UKKi017-C (NP0075-11B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6337. UKKi018-A (NP0080-2B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6338. UKKi018-B (NP0080-6A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6339. UKKi018-C (NP0080-8B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6340. UKKi019-A (NP0081-1A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6341. UKKi019-B (NP0081-11)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6342. UKKi019-C (NP0081-12C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6343. UKKi020-A (NP0100-4)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6344. UKKi020-B (NP0100-8)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6345. UKKi020-C (NP0100-10E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6346. UKKi020-D (NP0100-11)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6347. UKKi021-A (NP0105-2)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6348. UKKi021-B (NP0105-19)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6349. UKKi022-A (NP0106-34)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6350. UKKi022-C (NP0106-10A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6351. UKKi022-D (NP0106-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6352. UKKi023-A (NP0126-1)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6353. UKKi023-B (NP0126-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6354. UKKi023-C (NP0126-6)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6355. UKKi024-A (NP0133-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6356. UKKi024-B (NP0133-1)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6357. UKKi024-C (NP0133-4)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6358. UKKi025-A (NP0135-1)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6359. UKKi025-B (NP0135-2)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6360. UKKi025-C (NP0135-7)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6361. UKKi026-A (NP0114-1A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6362. UKKi026-B (NP0114-2C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6363. UKKi026-C (NP0114-5E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6364. UKKi027-A (NP0101-A and NP0101-3D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6365. UKKi027-B (NP0101-B and NP0101-4C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6366. UKKi027-C (NP0101-C and NP0101-10H)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6367. UKKi028-A (NP0115-A and NP0115-4)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6368. UKKi028-B (NP0115-B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6369. UKKi028-C (NP0115-C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6370. UKKi029-A (NP0077-6D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6371. UKKi029-B (NP0077-16E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6372. UKKi029-C (NP0077-18C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6373. UKKi030-A (NP0134-6D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6374. UKKi030-B (NP0134-18A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6375. UKKi030-C (NP0134-26B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6376. UKKi031-A (NP0138-8B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6377. UKKi031-B (NP0138-19E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6378. UKKi031-C (NP0138-31B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6379. UKKi032-A (NP0141-12C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6380. UKKi032-B (NP0141-17A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6381. UKKi032-C (NP0141-31B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6382. UKKi034-A (NP0079-A and NP0079-7B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6383. UKKi034-B (NP0079-B and NP0079-15B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6384. UKKi034-C (NP0079-C and NP0079-16H)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6385. UKKi035-A (NP0139-A and NP0139-3E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6386. UKKi035-B (NP0139-B and NP0139-6C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6387. UKKi035-C (NP0139-C and NP0139-24D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6388. UKKi036-A (NP0143-A and NP0143-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6389. UKKi036-B (NP0143-B and NP0143-15)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6390. UKKi036-C (NP0143-C and NP0143-18)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6391. UKKi037-A (NP0144-A and NP0144-32)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6392. UKKi037-B (NP0144-B and NP0144-33)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6393. UKKi037-C (NP0144-C and NP0144-41)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6394. UKMi003-A

    Germany University Hospital Muenster (UKM)
    Disease:

    Sinus bradycardia

  6395. UKMi004-A

    Germany University Hospital Muenster (UKM)
    Disease:

    Normal (average)

  6396. UKMi005-A

    Germany University Hospital Muenster (UKM)
    Disease:

    Sinus node dysfunction

  6397. UKMi009-A (HCN4 K1 homo)

    Germany University Hospital Muenster (UKM)
    Disease:

    Sick sinus syndrome

  6398. UKMi011-A (HCN4 K1 hetero)

    Germany University Hospital Muenster (UKM)
    Disease:

    Sick sinus syndrome

  6399. UKWi008-A (PARK2-9 CL12)

    Germany Universitätsklinikum Würzburg (UKW)
    Disease:

    Attention deficit-hyperactivity disorder

  6400. UKWi008-A-1 (PARK2-9 CL22)

    Germany Universitätsklinikum Würzburg (UKW)
    Disease:

    Attention deficit-hyperactivity disorder

  6401. UKWi009-A (SK310 CL1)

    Germany Universitätsklinikum Würzburg (UKW)
    Disease:

    Normal (average)

  6402. UKWi009-A-1 (SK310 CL5)

    Germany Universitätsklinikum Würzburg (UKW)
    Disease:

    Normal (average)

  6403. UKWMPi001-A

    Germany Division of Molecular Psychiatry, Center of Mental Health (UKWMP)
    Disease:

    Normal (average)

  6404. UKWMPi015-A

    Germany Division of Molecular Psychiatry, Center of Mental Health (UKWMP)
    Disease:

    Depression

  6405. UKWMPi016-A

    Germany Division of Molecular Psychiatry, Center of Mental Health (UKWMP)
    Disease:

    Attention deficit-hyperactivity disorder

  6406. UKWMPi017-A

    Germany Division of Molecular Psychiatry, Center of Mental Health (UKWMP)

  6407. UKWMPi018-A

    Germany Division of Molecular Psychiatry, Center of Mental Health (UKWMP)

  6408. UKWMPi019-A

    Germany Division of Molecular Psychiatry, Center of Mental Health (UKWMP)

  6409. UKWNLi006-A (GLA-D170N-iPSC-1, FD1089/20 and GLA-508G>A-1)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6410. UKWNLi006-B (GLA-D170N-iPSC-2, GLA-508G>A-2 and FD1089/21)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6411. UKWNLi007-A (GLA-515G>A-1, GLA-C172Y-iPSC-1 and FD1210/1)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6412. UKWNLi007-B (GLA-515-G>A-2, FD1210/2 and GLA-C172Y-iPSC-2)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6413. UKWNLi008-A (SFN 1097_2)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Small fiber neuropathy

  6414. UKWNLi008-B (SFN 1097_3)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Small fiber neuropathy

  6415. UKWNLi008-C (SFN 1097_5)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Small fiber neuropathy

  6416. UKWNLi009-A (TK8, FD-1 and FD_1052)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6417. UKWNLi009-A-1 (IsoTK8 and IsoFD-1)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6418. UKWNLi010-A (Bi093 Cl1)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  6419. UKWNLi010-B (Bi093 Cl5)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  6420. UKWNLi010-C (Bi093 Cl8)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  6421. ULBi002-A (Hel115.6)

    Belgium Université Libre de Bruxelles (ULB)
    Disease:

    Normal (average)

  6422. ULBi003-A (HEL46.11)

    Belgium Université Libre de Bruxelles (ULB)
    Disease:

    Normal (average)

  6423. ULBi004-A (AH4)

    Belgium Université Libre de Bruxelles (ULB)
    Disease:

    Normal (average)

  6424. ULEIi001-A

    Germany Leipzig University (ULEI)
    Disease:

    Normal (average)

  6425. UCSFi001-A-49 (YH653-MUT-1C8-HET and DYT1-HET-1C8)

    United States University of Louisiana at Lafayette (ULL)
    Disease:

    Autosomal dominant torsion dystonia 1

  6426. UCSFi001-A-50 (YH653-MUT-H6-HET and DYT1-HET-H6)

    United States University of Louisiana at Lafayette (ULL)
    Disease:

    Autosomal dominant torsion dystonia 1

  6427. UCSFi001-A-51 (YH653-MUT-2F2-HOMO and DYT1-HOMO-2F2)

    United States University of Louisiana at Lafayette (ULL)
    Disease:

    Autosomal dominant torsion dystonia 1

  6428. UMi035-A (GM07968)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Gaucher disease type 1

  6429. UMi036-A (ND34263)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Parkinson disease

  6430. UMi038-A

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer disease

  6431. UMi038-A-1

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer disease

  6432. UMi039-A

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6433. UMi039-A-1

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6434. UMi040-A (SB162-284 cl.1)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Auditory neuropathy spectrum disorder

  6435. UMi041-A (410730)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6436. UMi042-A

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6437. UMi042-A-1 (408737 CB9)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6438. UMi043-A (AD 381852 clone #1)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6439. UMi044-A (**1113.4)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Charcot-marie-tooth disease type 4b3

  6440. UMi045-A (**1159.1)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Charcot-marie-tooth disease type 4b3

  6441. UMi046-A (***1407.3)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Charcot-marie-tooth disease type 4b3

  6442. UMi047-A (sord1 DM)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy

  6443. UMi048-A (sord1 GB)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy

  6444. UMi049-A (IIsord1 RV)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy

  6445. UMi050-A (417027 clone 8)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer disease

  6446. UMi050-B (417027 clone 3)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer disease

  6447. UMi052-A (PLS405757 Cl#3)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Primary lateral sclerosis

  6448. UMi053-A (PLS405714 Cl#4)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Primary lateral sclerosis

  6449. UMi054-A

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Spinocerebellar ataxia 27b

  6450. UMi055-A

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Spinocerebellar ataxia 27b

  6451. UMi056-A

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Spinocerebellar ataxia 27b

  6452. UMANi255-A (NB221c)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Foveal hypoplasia

  6453. UMANi255-A-1 (PS02b-B6)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Foveal hypoplasia

  6454. UMANi257-A (AGD-14-01)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Cadasil

  6455. UMANi258-A (AGD-14-04)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Cadasil

  6456. UMANCi001-A (TF173B)

    United Kingdom C2T-Kimber lab (UMANC)
    Disease:

    Normal (average)

  6457. UMANCi002-A (TF172D)

    United Kingdom C2T-Kimber lab (UMANC)
    Disease:

    Hnf1b

  6458. UMANCi003-A (TF171A)

    United Kingdom C2T-Kimber lab (UMANC)
    Disease:

    Hnf1b

  6459. UMCGi001-A (PPCM RC1 c1)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6460. UMCGi001-B (PPCM RC1 c2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6461. UMCGi002-A (CTP1-C1)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Cardiomyopathy

  6462. UMCGi002-B (CTP1-C2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Cardiomyopathy

  6463. UMCGi002-C (CTP1-C3)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Cardiomyopathy

  6464. UMCGi003-A (PPCM RP1 c1)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Obsolete_peripartum cardiomyopathy

  6465. UMCGi003-B (PPCM RP1 c3)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Obsolete_peripartum cardiomyopathy

  6466. UMCGi004-A (PPCM RC2 c1)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6467. UMCGi004-B (PPCM RC2 c2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6468. UMCGi005-A (PPCM RP2 c2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Obsolete_peripartum cardiomyopathy

  6469. UMCGi005-B (PPCM RP2 c9)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Obsolete_peripartum cardiomyopathy

  6470. UMCGi006-A (DRP1-C2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6471. UMCGi006-B (DRP1-C3)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6472. UMCGi007-A (DRP2-C2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6473. UMCGi007-B (DRP2-C4)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6474. UMCGi008-A (DRP3-C5)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6475. UMCGi008-B (DRP3-C7)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6476. UMCGi008-C (DRP3-C10)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6477. UMCGi008-D (DRP3-C11)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6478. UMCGi009-A (PLN2-C2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Cardiomyopathy

  6479. UMCGi011-A (CTP2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  6480. UMCGi011-B (CTP2-C5)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  6481. UMCGi011-C (CTP2-C4)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  6482. UMCGi012-A (UMCG-PD-iPSC-T369M)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Parkinson disease

  6483. UMCGi013-A (UMCG-PD-iPSC-E326K)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Parkinson disease

  6484. UMCGi014-A (UMCG-PD-iPSC-nonGBA1/A)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Parkinson disease

  6485. UMCGi015-A (UMCG-PD-iPSC-nonGBA1/B)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Parkinson disease

  6486. UMCGi016-A (CTP3-C3)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  6487. UMCGi016-B

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  6488. UMCUi001-A (CRYAB-A527G-11C1)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Dilated cardiomyopathy 1ii

  6489. UMCUi002-A (CRYAB-A527G-12C6)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Dilated cardiomyopathy 1ii

  6490. UMCUi003-A (CRYAB-A527G-91C10)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Dilated cardiomyopathy 1ii

  6491. UMCUi004-A (CRYAB-A527G-92C25)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6492. UMCUi005-A (aPLN-R14del-GR04C1)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Cardiomyopathy

  6493. UMCUi006-A (PLN-GR05C5)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6494. UMCUi007-A (84C12)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Aortic dissection

  6495. UMCUi008-A (86C6)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Aortic root aneurysm

  6496. UMCUi009-A (87C3)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6497. UMCUi010-A (88C6)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6498. UMCUi011-A (119C9)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Aortic root aneurysm

  6499. UMCUi012-A (aPLN-R14del-GR02C8)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Cardiomyopathy

  6500. UMCUi013-A (TNNI3 P1C26)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Restrictive cardiomyopathy

  6501. UMCUi014-A (TNNI3 P2C27)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Restrictive cardiomyopathy

  6502. UMCUi015-A (TNNI3 C1C1)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6503. UMCUi016-A (TNNI3 C2C14)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6504. RUCDRi002-A-73 (IPSC-CraCCER and LiPSC-GR1.1-CraCCER, TC-1133-CraCCER)

    Germany University Medical Center Goettingen (UMG)
    Disease:

    Normal (average)

  6505. RUCDRi002-A-74 (Myo-CCER and IPSC-Myo-CCER, LiPSC-GR1.1-Myo-CCER, TC-1133-Myo-CCER)

    Germany University Medical Center Goettingen (UMG)
    Disease:

    Normal (average)

  6506. UMGACBi001-A

    Germany Institute of Anatomy and Cell Biology (UMGACB)

  6507. MHHi001-A-12 (Phx_SRCAP_g3_1200_4)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  6508. MHHi001-A-13 (Phx_SRCAP_g3_1200_7)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  6509. MHHi001-A-14 (Phx_SRCAP_g3_1400_6/8)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities

  6510. MHHi001-A-16 (PHX_CRISPR_JR_DIS10)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities

  6511. MHHi001-A-17 (PHX_CRISPR_JR_DIS13)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities

  6512. UMGWi001-B (Z1 K3v3)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Floating-harbor syndrome

  6513. UMGWi004-A (BNH1 _iPSC_WT_8)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  6514. UMGWi004-B (BNH1 _iPSC_WT_48)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  6515. UMGWi004-B-1 (BNH1_iPSC_FHS1_cr_well7_JR)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Floating-harbor syndrome

  6516. UMGWi004-B-2 (BNH1_iPSC_FHS1_cr_well12_JR)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Floating-harbor syndrome

  6517. UMGWi004-B-3

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Non-syndromic intellectual disability

  6518. UMGWi004-B-4

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Non-syndromic intellectual disability

  6519. UMICHi001-A (HVRDi004-B, GM23338 and PGP1 Parental)

    United States University of Michigan (UMICH)
    Disease:

    Normal (average)

  6520. UMICHi001-A-1 (ITPR1 Wildtype and UMICHi001-AB)

    United States University of Michigan (UMICH)
    Disease:

    Normal (average)

  6521. UMICHi001-A-2 (ITPR1 Het and ITPR1+/-)

    United States University of Michigan (UMICH)
    Disease:

    Spinocerebellar ataxia type 15/16

  6522. UMILi001-A (KAB07)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  6523. UMILi002-A (KAB01)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  6524. UMILi003-A (KAB03)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  6525. UMILi004-A (KAB04)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  6526. UMILi005-A (KAB05)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  6527. UMILi006-A (CTL05)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6528. UMILi007-A (CTL06)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6529. UMILi008-A (CTL07)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6530. UMILi009-A (GAD02)

    Italy University of Milan (UMIL)
    Disease:

    Gabriele-de vries syndrome

  6531. UMILi010-A (GAD01)

    Italy University of Milan (UMIL)
    Disease:

    Gabriele-de vries syndrome

  6532. UMILi011-A (CTL10)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6533. UMILi012-A (WVS02)

    Italy University of Milan (UMIL)
    Disease:

    Weaver syndrome

  6534. UMILi013-A (WVS01)

    Italy University of Milan (UMIL)
    Disease:

    Weaver syndrome

  6535. UMILi014-A (WVS04)

    Italy University of Milan (UMIL)
    Disease:

    Weaver syndrome

  6536. UMILi015-A (WVS03)

    Italy University of Milan (UMIL)
    Disease:

    Weaver syndrome

  6537. UMILi016-A (DUP01)

    Italy University of Milan (UMIL)
    Disease:

    7q11.23 microduplication syndrome

  6538. UMILi017-A (DUP02)

    Italy University of Milan (UMIL)
    Disease:

    7q11.23 microduplication syndrome

  6539. UMILi018-A (DUP03)

    Italy University of Milan (UMIL)
    Disease:

    7q11.23 microduplication syndrome

  6540. UMILi019-A (DUP04)

    Italy University of Milan (UMIL)
    Disease:

    7q11.23 microduplication syndrome

  6541. UMILi020-A (WBS04)

    Italy University of Milan (UMIL)
    Disease:

    Williams-beuren syndrome

  6542. UMILi021-A (WBS03)

    Italy University of Milan (UMIL)
    Disease:

    Williams-beuren syndrome

  6543. UMILi022-A (WBS01)

    Italy University of Milan (UMIL)
    Disease:

    Williams-beuren syndrome

  6544. UMILi023-A (WBS02)

    Italy University of Milan (UMIL)
    Disease:

    Williams-beuren syndrome

  6545. UMILi024-A (CTL04)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6546. UMILi025-A (CTL09)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6547. UMILi026-A (CTL01)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6548. UMILi027-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6549. UMILi028-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6550. UMILi029-A (SHP1)

    Italy University of Milan (UMIL)
    Disease:

    Autosomal recessive limb-girdle muscular dystrophy-4

  6551. UMILi030-A (SHP2)

    Italy University of Milan (UMIL)
    Disease:

    Autosomal recessive limb-girdle muscular dystrophy-4

  6552. UMILi031-A (SHP3)

    Italy University of Milan (UMIL)
    Disease:

    Autosomal recessive limb-girdle muscular dystrophy-4

  6553. UMILi032-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6554. UMILi033-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6555. UMILi034-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6556. UMILi035-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6557. UMILi036-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6558. UMNi001-A (iPSC LUCAS1)

    United States University of Minnesota (UMN)
    Disease:

    Normal (average)

  6559. UNAMi001-A (IFC-UNAM iPD01-S)

    Mexico Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)
    Disease:

    Parkinson disease

  6560. UNAMi002-A (IFC-UNAM iPD02-S)

    Mexico Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)
    Disease:

    Parkinson disease

  6561. UNAMi003-A (IFC-UNAM iPD03-PINK1)

    Mexico Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)
    Disease:

    Parkinson disease

  6562. UNEWi001-A (UNEW001Ai)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6563. UNEWi002-A (UNEW002Ai and PRPF31 AW)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6564. UNEWi003-A (PRPF31-HD)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6565. UNEWi004-A (PRPF31 SH)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6566. UNEWi005-A (PRPF31 RH)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6567. UNEWi006-A

    United Kingdom University of Newcastle (UNEW)

  6568. UNEWi011-A (UNEW011Ai)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Cernunnos-xlf deficiency

  6569. UNEWi017-A

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Aplastic anemia

  6570. UNEWi018-A

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Aplastic anemia

  6571. UNEWi019-A

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Anemia

  6572. UNEWi021-A (F018 13.2)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6573. UNEWi021-B (F018 15.8)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6574. UNEWi021-C (F018 17/8-1)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6575. UNEWi022-A (F181 5.8)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6576. UNEWi022-B (F181 18.2)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6577. UNEWi022-C (F181 25.7)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6578. UNEWi023-A (F343 clone 2)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6579. UNEWi023-B (F343 clone 3)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6580. UNEWi023-C (F343 clone 4)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6581. UNEWi024-A (F180-1)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6582. UNEWi024-B (F180-2)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6583. UNEWi024-C (F180-3)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6584. UNEWi025-A (F324 5.8)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6585. UNEWi025-B (F324 12.8)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6586. UNEWi025-C (F324 19.7)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6587. UNEWi026-A (SF116 clone 1)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Age-related macular degeneration

  6588. UNEWi026-B (SF116 clone 2)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Age-related macular degeneration

  6589. UNEWi026-C (SF116 clone K)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Age-related macular degeneration

  6590. UNEWi027-A (F116)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6591. UNIBSi017-A (EDS-iPSC)

    Italy University of Brescia (UNIBS)

  6592. UNIBSi018-A

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6593. UNIBSi018-B

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6594. UNIBSi019-A

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6595. UNIBSi019-B

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6596. UNIBSi020-A

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6597. UNIBSi020-B

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6598. UNIFEi001-A (iPSca1N1, MARPiPSCA1N1 and UniFei001-A)

    Italy University of Ferrara (UNIFE)
    Disease:

    Spinocerebellar ataxia type 1

  6599. UNIFEi002-A (UNIFEi013-A, UniFei013-A, MARPiPSCA1N13 and iPSca1N13)

    Italy University of Ferrara (UNIFE)
    Disease:

    Spinocerebellar ataxia type 1

  6600. UNIMGi009-A (PD-1M)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Parkinson disease

  6601. UNIMGi010-A (PD-4F)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Parkinson disease

  6602. UNIMGi011-A (PD-2M)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Parkinson disease

  6603. UNIMGi012-A (PRICKLE2 MUTmild)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Epilepsy syndrome

  6604. UNIMGi013-A (PRICKLE2 MUTsevere)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Epilepsy syndrome

  6605. UNIONi001-A (UNION-ViPS-C2401022)

    China UNION STEM CELL & GENE ENGINEERING CO., LTD. (UNION)
    Disease:

    Normal (average)

  6606. UNIPDi004-A

    Italy University of Padova (UNIPD)
    Disease:

    Normal (average)

  6607. UNIPDi004-B (HDP04)

    Italy University of Padova (UNIPD)
    Disease:

    Normal (average)

  6608. UNIPDi005-A

    Italy University of Padova (UNIPD)
    Disease:

    Normal (average)

  6609. UNIPDi006-A

    Italy University of Padova (UNIPD)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  6610. UNIPDi008-A (FXS-GM05131)

    Italy University of Padova (UNIPD)
    Disease:

    Fragile x syndrome

  6611. UNIPDi008-B (FXS GM05131 primed)

    Italy University of Padova (UNIPD)
    Disease:

    Fragile x syndrome

  6612. UNIPDi009-A

    Italy University of Padova (UNIPD)
    Disease:

    Fragile x syndrome

  6613. UNIPDi010-B (Primed-555 FRX)

    Italy University of Padova (UNIPD)
    Disease:

    Fragile x syndrome

  6614. UNIPVi001-A (COR248 and NG2409)

    Italy Units of Biology and Genetics - University of Pavia (UNIPV)
    Disease:

    Joubert syndrome

  6615. UNIPVi002-A (HDF108)

    Italy Units of Biology and Genetics - University of Pavia (UNIPV)
    Disease:

    Normal (average)

  6616. UNIPVi003-A (HDF109)

    Italy Units of Biology and Genetics - University of Pavia (UNIPV)
    Disease:

    Normal (average)

  6617. UNIPVi004-A (COR316 and NG3157)

    Italy Units of Biology and Genetics - University of Pavia (UNIPV)
    Disease:

    Joubert syndrome

  6618. UNIZARi001-A (FiPSTK2-2)

    Spain University of Zaragoza (UNIZAR)
    Disease:

    Mitochondrial dna depletion syndrome, myopathic form

  6619. UOCi001-A (CIM001.4)

    Australia University of Calgary (UOC)

  6620. UOCi002-A (CIM008.6)

    Australia University of Calgary (UOC)

  6621. UOCi003-A (GPiPSC 31-1)

    Canada University of Calgary (UOC)
    Disease:

    Simplified gyral pattern

  6622. UOCi003-A-1 (A18 GPiPSC 31-1)

    Canada University of Calgary (UOC)
    Disease:

    Simplified gyral pattern

  6623. UOCi004-A

    Canada University of Calgary (UOC)
    Disease:

    Spondylocostal dysostosis

  6624. UOCi005-A

    Canada University of Calgary (UOC)
    Disease:

    Anencephaly

  6625. UODi001-A (ChiPS4 and ChiPSC4)

    United Kingdom University of Dundee (UOD)
    Disease:

    Normal (average)

  6626. UOFTi001-A (CT002)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6627. UOFTi003-A (CT004)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6628. UOFTi004-A (BD001)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6629. UOFTi005-A (BD002)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6630. UOFTi006-A (BD003)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6631. UOFTi007-A (MS002)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6632. UOFTi008-A (MS004)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6633. UOFTi009-A (MS012)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6634. UOFTi010-A (MS015)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

    Disease:

    Mitochondrial disease

  6635. UOFTi011-A (MS003)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6636. UOFTi012-A (MS006)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6637. UOFTi013-A (MS008)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6638. UOFTi014-A (MS009)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6639. UOFTi015-A (MS010)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6640. UOHi002-A (UOHi002 with its alternative name as UOHi002SHANK3)

    Israel University of Haifa (UOH)
    Disease:

    Normal (average)

  6641. UOHi003-A (UOHi001 with its alternative name as UOHi001SHANK3)

    Israel University of Haifa (UOH)
    Disease:

    Phelan-mcdermid syndrome

  6642. UOMi008-A (ACS-hiPSC-HPP2)

    Canada University of Manitoba (UOM)
    Disease:

    Hypophosphatasia

  6643. UOMi009-A (ACS-hiPSC-HPP3)

    Canada University of Manitoba (UOM)
    Disease:

    Hypophosphatasia

  6644. UOMi010-A (ANCS-hiPSC-HPP5)

    Canada University of Manitoba (UOM)
    Disease:

    Hypophosphatasia

  6645. UOMi011-A (ANCS-hiPSC-HPP6)

    Canada University of Manitoba (UOM)
    Disease:

    Hypophosphatasia

  6646. UOMi012-A (NAAS-hiPSC-Fontan1)

    Canada University of Manitoba (UOM)
    Disease:

    Fontan procedure

  6647. UOMi013-A (GSACS-hiPSC-MELAS7)

    Canada University of Manitoba (UOM)
    Disease:

    Melas syndrome

  6648. UOMi015-A (GSACS-hiPSC-MELAS_S5)

    Canada University of Manitoba (UOM)
    Disease:

    Melas syndrome

  6649. UOSi001-A (MIFF1, ShiPS-MIFF1 and MIFF-1)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  6650. UOSi001-B (MIFF3, MIFF-3 and ShiPS-MIFF3)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  6651. UTSWi001-A-2 (FA1-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6652. UTSWi001-A-3 (FA1ic-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6653. UTSWi002-A-2 (FA2-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6654. UTSWi002-A-3 (FA2ic-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6655. UTSWi003-A-2 (FA3-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6656. UTSWi003-A-3 (FA3ic-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6657. UOXFi001-A (MK071-1)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6658. UOXFi001-B (MK071-3)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6659. UOXFi001-C (MK071-5)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6660. UOXFi001-D (MK071-6)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6661. UOXFi002-A (MK082-26)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6662. UOXFi002-B (MK082-30)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6663. UOXFi003-A (MK088-1)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6664. UOXFi003-C (MK088-7)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6665. UOXFi004-A (OX1-18)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6666. UOXFi004-B (OX1-19)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6667. UOXFi005-A (JR053-1 and SAMEA4453899)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6668. UOXFi005-B (JR053-6)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6669. UOXFi006-A (OX2-28)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6670. UOXFi007-A (MK002-4)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6671. UOXFi007-B (MK002-6)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6672. UOXFi007-C (MK002-7)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6673. UOXFi008-A (MK144-1)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6674. UOXFi008-B (MK144-7)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6675. UOXFi008-C (MK144-10)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6676. UOXFi009-A (MK024-3)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6677. UOXFi009-B (MK024-4)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6678. UOXFi009-C (MK024-9)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6679. UOXFi010-A (JR023-1)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6680. UOXFi010-B (JR023-2)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6681. UOXFi010-C (JR023-5)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6682. UOXFi010-D (JR023-7)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6683. STBCi063-A-1 (SFC856-03-04 PINK1-/-A12)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6684. STBCi063-A-2 (SFC856-03-04 STING-/-F11D1)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6685. STBCi324-A-1 (SFC826-04-06 STING-/-B12)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6686. UPITTi004-A (CN090 C5A5J2)

    United States University of Pittsburgh (UPITT)
    Disease:

    Sickle cell anemia

  6687. UPITTi004-B (CN090 C1B5B5)

    United States University of Pittsburgh (UPITT)
    Disease:

    Sickle cell anemia

  6688. UPITTi005-A (MAGE112_Clone16)

    United States University of Pittsburgh (UPITT)
    Disease:

    Sickle cell anemia

  6689. UPITTi005-B (MAGE112_Clone17)

    United States University of Pittsburgh (UPITT)
    Disease:

    Sickle cell anemia

  6690. UPSFRi001-A (PB03)

    France Université Paris-Sud 11 (UPSFR)

  6691. UPSFRi002-A (PB04)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Beta thalassemia

  6692. UPSFRi003-A (PB05-1)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Beta thalassemia

  6693. UPSFRi004-A (PB05)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Beta thalassemia

  6694. UPSFRi004-A-1 (PB05-1)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Beta thalassemia

  6695. UPSFRi005-A (PB06)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Obsolete_down syndrome

  6696. UPSFRi005-A-1 (PB06-1)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Obsolete_down syndrome

  6697. UPSFRi006-A (PB07)

    France Université Paris-Sud 11 (UPSFR)

  6698. UPSFRi007-A (PB08)

    France Université Paris-Sud 11 (UPSFR)

  6699. UPSFRi008-A (PB09)

    France Université Paris-Sud 11 (UPSFR)

  6700. UPSFRi009-A (PB10)

    France Université Paris-Sud 11 (UPSFR)

  6701. UQi001-A (C11-WT)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6702. UQi001-A-1 (C11-TDP43-A382T)

    Australia The University of Queensland (UQ)
    Disease:

    Amyotrophic lateral sclerosis

  6703. UCSFi001-A-1O (dPRO)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6704. UCSFi001-A-1P (dLAMA)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6705. UCSFi001-A-1Q (dGFP)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6706. UQi002-A (C3)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6707. UQi003-A (C7)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6708. UQi004-A (C12)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6709. UQi005-A (C13)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6710. UQi006-A (M2)

    Australia The University of Queensland (UQ)
    Disease:

    Amyotrophic lateral sclerosis

  6711. UQi007-A (M4)

    Australia The University of Queensland (UQ)
    Disease:

    Amyotrophic lateral sclerosis

  6712. UQi008-A (M8)

    Australia The University of Queensland (UQ)
    Disease:

    Amyotrophic lateral sclerosis

  6713. UQi009-A (M15)

    Australia The University of Queensland (UQ)
    Disease:

    Amyotrophic lateral sclerosis

  6714. UQACi001-A (iPSC-EBS21)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6715. UQACi002-A (iPSC-EBS1)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6716. UQACi003-A (iPSC-EBS2)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6717. UQACi004-A (iPSC-EBS9)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6718. UQACi005-A (iPSC-EBS10)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6719. UQACi006-A (iPSC-EBS26)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6720. UQACi007-A (iPSC-EBS29)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6721. URi001-A

    Japan University of the Ryukyus (UR)
    Disease:

    Major depressive disorder

  6722. URi002-A

    Japan University of the Ryukyus (UR)
    Disease:

    Bipolar disorder

  6723. URi004-A

    Japan University of the Ryukyus (UR)
    Disease:

    Normal (average)

  6724. URi005-A

    Japan University of the Ryukyus (UR)
    Disease:

    Bipolar disorder

  6725. USCBi001-A (NIBSC_i008, NIBSC8,)

    United Kingdom National Institute for Biological Standards and Control - UK Stem Cell Bank (USCB)
    Disease:

    Normal (average)

  6726. USFi001-A (1CN1.5)

    United States University of South Florida (USF)
    Disease:

    Friedreich ataxia

  6727. USFi002-A (0AS1)

    United States University of South Florida (USF)
    Disease:

    Dilated cardiomyopathy

  6728. USFi003-A (1AB1)

    United States University of South Florida (USF)
    Disease:

    Dilated cardiomyopathy

  6729. USFi004-A (3IV6)

    United States University of South Florida (USF)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  6730. USFi005-A (CUUSFi001-A and LQT1)

    United States University of South Florida (USF)

  6731. USFi006-A (CUUSFi002-A and LQT2)

    United States University of South Florida (USF)
    Disease:

    Normal (average)

  6732. USFi007-A (CUUSFi003-A and LQT3)

    United States University of South Florida (USF)
    Disease:

    Normal (average)

  6733. USPi001-A (iPS_LGH_AHDC1_P1)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Xia-gibbs syndrome

  6734. USPi002-A (iPS_LGH_AHDC1_P2)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Xia-gibbs syndrome

  6735. USPi003-A (iPS_LGH_AHDC1_P3)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Xia-gibbs syndrome

  6736. USPi004-A (DFNA58-ipsc-con1-cl4)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Normal (average)

  6737. USPi005-A (DFNA58-ipsc-con2-cl1)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Normal (average)

  6738. USPi006-A (DFNA58-ipsc-dup1-cl2)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Autosomal dominant nonsyndromic deafness 58

  6739. USPi007-A (DFNA58-ipsc-dup2-cl5)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Autosomal dominant nonsyndromic deafness 58

  6740. UTHSCHi001-A (NDC-AD01)

    United States The University of Texas Health Science Center at Houston (UTHSCH)
    Disease:

    Alzheimer's disease

  6741. UTSWi001-A (FA1)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6742. UTSWi001-A-1 (FA1ic)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6743. UTSWi002-A (FA2)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6744. UTSWi002-A-1 (FA2ic)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6745. UTSWi003-A (FA3)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6746. UTSWi003-A-1 (FA3ic)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6747. UTSWi004-A

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6748. UTUi001-A (TUR1)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  6749. UTUi001-B (TUR2)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  6750. UTUi001-C (TUR3)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  6751. UTUi002-A (TUR-STAB1-B1)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  6752. UTUi003-A (TUR-B1)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  6753. VANYHHi001-A (AF13_VANYHH)

    United States VA New York Harbor Healthcare System (VANYHH)
    Disease:

    Brugada syndrome

  6754. VAPACLi001-A

    United States Veterans Affairs Palo Alto Health Care System: Chen Lab (VAPACL)
    Disease:

    Coronary artery vasospasm

  6755. VAPACLi002-A

    United States Veterans Affairs Palo Alto Health Care System: Chen Lab (VAPACL)
    Disease:

    Coronary artery vasospasm

  6756. VAPACLi003-A

    United States Veterans Affairs Palo Alto Health Care System: Chen Lab (VAPACL)
    Disease:

    Coronary artery vasospasm

  6757. VCCRIi002-A (069)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Spontaneous coronary artery dissection

    Disease:

    Obsolete_fibromuscular dysplasia

  6758. VCCRIi003-A (SCAD-96 and 096)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Spontaneous coronary artery dissection

    Disease:

    Celiac disease

  6759. VCCRIi018-A (136 and SCAD-136)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Spontaneous coronary artery dissection

  6760. VCCRIi024-A (326)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Normal (average)

  6761. VCCRIi043-A (453)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Niemann-pick disease, type c1

  6762. VCCRIi044-A (871)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Niemann-pick disease, type c1

  6763. VHIRi001-A (C1(RP25)_UiPSC_mR5F_7)

    Spain Vall d'Hebron Institut de Recerca (VHIR)
    Disease:

    Normal (average)

  6764. VHIRi002-A (C2(RP25)_UiPSC_mR5F_1)

    Spain Vall d'Hebron Institut de Recerca (VHIR)
    Disease:

    Normal (average)

  6765. VHIRi003-A (RP25_UiPSC_mR5F_8)

    Spain Vall d'Hebron Institut de Recerca (VHIR)
    Disease:

    Normal (average)

  6766. VRFi001-A (VRF-RBiPSC01)

    India VISION RESEARCH FOUNDATION (VRF)
    Disease:

    Retinoblastoma

  6767. VRISGi002-A

    Vietnam Vinmec Research Insitute of Stem Cell and Gene Technology (VRISG)
    Disease:

    Normal (average)

  6768. VRISGi004-A (ERY02-hiPSC-CL)

    Vietnam Vinmec Research Insitute of Stem Cell and Gene Technology (VRISG)
    Disease:

    Normal (average)

  6769. VUi001-A (SCZ 14.3 and hvs479)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6770. VUi002-A (SCZ 18.10 and hvs483)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6771. VUi003-A (SCZ 13.2 and hvs478)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6772. VUi004-A (SCZ 19.2 and hvs-484)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6773. VUi005-A (787.3)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6774. VUi006-A (SCZ 21.5)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6775. VUi007-A (786.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6776. VUi008-A (SCZ 6.2)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6777. VUi009-A (SCZ 10.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6778. VUi010-A (SCZ 1.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6779. VUi011-A (SCZ 3.5)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6780. VUi012-A (SCZ 7.2)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6781. VUi013-A (804.3)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6782. VUi014-A (SCZ 11.8 and hvs476)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6783. VUi015-A (SCZ 12.1 and hvs-477)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6784. VUi016-A (789.A1 and hvs341)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6785. VUi017-A (SCZ4.3)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6786. VUi018-A (SCZ 5.1 and hvs487)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6787. VUi019-A (SCZ 15.2 and hvs480)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6788. VUi020-A (SCZ 20.1 and hvs485)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6789. VUi021-A (793.3 and hvs473)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6790. VUi023-A (801.A1 and hvs474)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6791. VUi024-A (SCZ 9.4)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6792. VUi025-A (hvs93)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6793. VUi026-A (hvs97)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6794. VUi027-A (hvs201)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6795. VUi028-A (hvs369)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6796. VUi029-A (hvs449a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6797. VUi030-A (hvs450a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6798. VUi031-A (hvs88)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6799. VUi032-A (GM23973 Coriell and hvs451a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6800. VUi033-A (hvs445a and GM02036 Coriell)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6801. VUi034-A (hvs-304 and SCZ 8.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6802. VUi035-A (hvs-471 and SCZ 802.2A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6803. VUi036-A (hvs420 and GM23964)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6804. VUi038-A (hvs444a and GM01651 Coriell)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6805. VUi039-A (hvs446a and GM05381 Coriell)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6806. VUi040-A (GB3g)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6807. VUi040-B (GB3f)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6808. VUi041-A (GB4d)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6809. VUi041-B (GB4b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6810. VUi042-A (GB2a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6811. VUi042-B (GB2f)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6812. VUi047-A (785.10 and hvs337)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6813. VUi048-A (788.A1 and hvs469)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6814. VUi049-A (790.3 and hvs470)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6815. VUi052-A (17.6 and hvs482)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6816. VUi053-A (2.5 and hvs317)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6817. VUi058-A (hvs521a and PEX1-024)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Zellweger spectrum disorders

  6818. VUi059-A (hsv522a and PEX1-025)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Zellweger spectrum disorders

  6819. VUi060-A (hsv523a and PEX1-026)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Zellweger spectrum disorders

  6820. VUi062-A (hvs512b and 7485267)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6821. VUi062-B (hvs512c and 7485267)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6822. VUi062-C (hvs512d and 7485267)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6823. VUi063-A (6300896 and hvs513a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6824. VUi063-B (hvs513b and 6300896)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6825. VUi063-C (hvs513c and 6300896)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6826. VUi064-A (1484443 and hvs514a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6827. VUi064-B (1484443 and hvs514b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6828. VUi064-C (hvs514c and 1484443)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6829. VUi067-A (785162, hvs462a and 328.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6830. VUi068-A (747417, 238.A and hvs463a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6831. VUi069-A (747412, hvs464b and 237.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6832. VUi069-B (747412, 237.A and hvs464a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6833. VUi070-A (773097, hvs465b and 298.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6834. VUi070-B (773097, hvs465a and 298.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6835. VUi071-A (776649, hvs466b and 307.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6836. VUi071-B (776649, hvs466a and 307.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6837. VUi072-A (hvs467a, 773099 and 297.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6838. VUi073-A (hvs468a, 712461 and 157.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6839. VUi074-A (689209, hvs497a and 113.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6840. VUi074-B (689209, hvs497b and 113.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6841. VUi074-C (689209, 113.C and hvs497c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6842. VUi075-A (105.A, hvs498a and 685694)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6843. VUi075-B (105.B, hvs498b and 685694)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6844. VUi075-C (105.C, hvs498c and 685694)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6845. VUi076-A (1005528, 509.A and hvs499a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6846. VUi076-B (1005528, hvs499b and 509.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6847. VUi076-C (1005528, 509.C and hvs499c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6848. VUi077-A (hvs500a, 781085 and 315.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6849. VUi077-B (hvs500b, 781085 and 315.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6850. VUi077-C (hvs500c, 315.C and 781085)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6851. VUi078-A (hvs501a, 710274 and 152.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6852. VUi078-B (hvs501b, 152.B and 710274)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6853. VUi078-C (hvs501c, 152.C and 710274)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6854. VUi079-A (894067, 470.A and hvs502a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6855. VUi079-B (hvs502b, 894067 and 470.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6856. VUi079-C (hvs502c, 894067 and 470.C)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6857. VUi080-A (293.A, 770533 and hvs503a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6858. VUi080-B (293.B, 770533 and hvs503b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6859. VUi080-C (hvs503c, 293.C and 770533)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6860. VUi081-A (379.A, 837936 and hvs504a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6861. VUi081-B (379.B, 837936 and hvs504b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6862. VUi081-C (379.C, 837936 and hvs504c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6863. VUi082-A (778144, 311.A and hvs505a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6864. VUi082-B (778144, 311.B and hvs505b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6865. VUi082-C (778144, 311.C and hvs505c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6866. VUi083-A (800835, hvs506a and 339.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6867. VUi083-B (800835, 339.B and hvs506b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6868. VUi083-C (800835, 339.C and hvs506c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6869. VUi084-A (674780, hvs507a and 78.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6870. VUi084-B (674780, hvs507b and 78.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6871. VUi084-C (674780, hvs507c and 78.C)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6872. VUi085-A (717583, hvs508a and 175.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6873. VUi085-B (717583, hvs508b and 175.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6874. VUi085-C (717583, 175.C and hvs508c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6875. VUi086-A (738705, hvs509a and 217.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6876. VUi086-B (738705, hvs509b and 217.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6877. VUi086-C (738705, 217.C and hvs509c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6878. VUi087-A (hvs510a, 776639 and 305.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6879. VUi087-B (hvs510b, 305.B and 776639)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6880. VUi087-C (hvs510c, 305.C and 776639)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6881. VUi088-A (hvs515a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6882. VUi088-B (hvs515b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6883. VUi088-C (hvs515c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6884. VUi089-A (hvs-481 and 16.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6885. VUi090-A (hvs533a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6886. VUi090-B (hvs533b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6887. VUi090-C (hvs533c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6888. VUi093-A (hvs472 and 771.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6889. VUi094-A (2086640 and hvs536a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Grin2b-related complex neurodevelopmental disorder

  6890. VUi095-A (71066723 and hvs538c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Hao-fountain syndrome

  6891. VUi095-B (hvs538b and 71066723)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Hao-fountain syndrome

  6892. VUi095-C (71066723 and hvs538a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Hao-fountain syndrome

  6893. VUi096-A (hvs542a and 1224409)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Clark-baraitser syndrome

  6894. VUi096-B (hvs542b and 1224409)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Clark-baraitser syndrome

  6895. VUi096-C (hvs542c and 1224409)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Clark-baraitser syndrome

  6896. VUi097-A (hvs557c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Hao-fountain syndrome

  6897. VUi097-B (hvs557b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Hao-fountain syndrome

  6898. VUi097-C (hvs557a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Hao-fountain syndrome

  6899. VUi098-A (hvs540a and 1286810)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Proximal 16p11.2 microdeletion syndrome

  6900. VUi098-B (hvs540b and 1286810)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Proximal 16p11.2 microdeletion syndrome

  6901. VUi098-C (hvs540c and 1286810)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Proximal 16p11.2 microdeletion syndrome

  6902. VUi099-A (1885222 and hvs560a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6903. VUi099-B (1885222 and hvs560b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6904. VUi099-C (1885222 and hvs560c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6905. VUi100-A (hvs577a and 2018125)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6906. VUi100-B (hvs577b and 2018125)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6907. VUi100-C (hvs577c and 2018125)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6908. VUi101-A (hvs575a and 2393801)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6909. VUi101-B (hvs575b and 2393801)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6910. VUi101-C (hvs575c and 2393801)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6911. VUi102-A (hvs578a and 9651968)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6912. VUi102-B (hvs578b and 9651968)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6913. VUi102-C (hvs578c and 9651968)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6914. VUi103-A (hvs543a and MDN 8482277)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6915. VUi103-B (hvs543b and MDN 8482277)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6916. VUi103-C (MDN 8482277 and hvs543c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6917. VUi104-A (hvs576a and 8815829)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6918. VUi104-B (hvs576b and 8815829)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6919. VUi104-C (hvs576c and 8815829)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6920. VUi105-A (hvs554a and 7480393)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6921. VUi105-B (hvs554b and 7480393)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6922. VUi105-C (hvs554c and 7480393)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6923. VUi106-A (hvs555a and 3152004)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6924. VUi106-B (hvs555b and 3152004)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6925. VUi106-C (hvs555c and 3152004)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6926. VUi107-A (hvs556a and 4226880)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6927. VUi107-B (hvs556b and 4226880)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6928. VUi107-C (hvs556c and 4226880)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6929. VUi108-A (2086636 and hvs516a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Grin2b-related complex neurodevelopmental disorder

  6930. VUi109-A (hvs517a and 2392816)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6931. VUi110-A (2124811 and hvs525a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Grin2b-related complex neurodevelopmental disorder

  6932. VUi111-A (6888827 and hvs526a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6933. VUi112-A (2086611 and hvs528a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Grin2b-related complex neurodevelopmental disorder

  6934. VUi113-A (2407481 and hvs529a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6935. VUi114-A (hvs531a and 2883755)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Grin2b-related complex neurodevelopmental disorder

  6936. VUi115-A (2086627 and hvs532b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Grin2b-related complex neurodevelopmental disorder

  6937. VUi116-A (hvs534a and 2196285)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Grin2b-related complex neurodevelopmental disorder

  6938. VUi117-A (2415610 and hvs535a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6939. VUi118-A (hvs537a and 1808890)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6940. CIGLi001-A-2

    Lithuania Vilnius University (VULSC)
    Disease:

    Normal (average)

  6941. CIGLi001-A-6 (VULSCi002-A-6)

    Lithuania Vilnius University (VULSC)
    Disease:

    Normal (average)

  6942. VUMCi001-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6943. VUMCi002-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6944. VUMCi003-A (1167)

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6945. VUMCi004-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6946. VUMCi005-A (3360)

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6947. VUMCi006-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6948. VUMCCVi001-A (NS15C5)

    United States Vanderbilt University Medical Center: Cardiovascular Medicine (VUMCCV)
    Disease:

    Normal (average)

  6949. VUMCCVi002-A (NS9C4)

    United States Vanderbilt University Medical Center: Cardiovascular Medicine (VUMCCV)
    Disease:

    Aortic valve stenosis

    Disease:

    Dyslipidemia

    Disease:

    Hypertension

  6950. VUMCCVi003-A (NS18C1)

    United States Vanderbilt University Medical Center: Cardiovascular Medicine (VUMCCV)
    Disease:

    Normal (average)

  6951. VUMCCVi004-A (NS8C1)

    United States Vanderbilt University Medical Center: Cardiovascular Medicine (VUMCCV)
    Disease:

    Coronary artery disease

    Disease:

    Hyperlipidemia

    Disease:

    Atrial fibrillation

  6952. WAi001-A (DF19-9-11T and iPS DF19-9-11T.H)

    United States WiCell Research Institute (WA)
    Disease:

    Normal (average)

  6953. WAi001-B (DF19-9-7T and iPS-DF19-9-7T)

    United States WiCell Research Institute (WA)
    Disease:

    Normal (average)

  6954. WCHi001-A

    China West China Hospital (WCH)
    Disease:

    Normal (average)

  6955. WCHi002-A

    China West China Hospital (WCH)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  6956. WCHi003-A

    China West China Hospital (WCH)
    Disease:

    Schizophrenia

  6957. WCHi004-A

    China West China Hospital (WCH)
    Disease:

    Normal (average)

  6958. WCHi005-A

    China West China Hospital (WCH)
    Disease:

    Bipolar disorder

  6959. WCHi006-A

    China West China Hospital (WCH)
    Disease:

    Schizophrenia

  6960. WCHPSYi001-A

    China Psychiatry Laboratory, West China Hospital, Sichuan University (WCHPSY)
    Disease:

    Schizophrenia

  6961. WCHPSYi002-A

    China Psychiatry Laboratory, West China Hospital, Sichuan University (WCHPSY)
    Disease:

    Schizophrenia

  6962. WIMRi001-A (PKU_LCL_11195)

    Australia Westmead Institute for Medical Research (WIMR)
    Disease:

    Phenylketonuria

  6963. WIMRi002-A (PKU_LCL_01565)

    Australia Westmead Institute for Medical Research (WIMR)
    Disease:

    Phenylketonuria

  6964. WIMRi003-A (PKU_FIB_00937)

    Australia Westmead Institute for Medical Research (WIMR)
    Disease:

    Phenylketonuria

  6965. WIMRi004-A (PKU_FIB_02406)

    Australia Westmead Institute for Medical Research (WIMR)
    Disease:

    Phenylketonuria

  6966. WISi005-A (BF1)

    Israel Weizmann Institute of Science (WIS)
    Disease:

    Normal (average)

  6967. WISi006-A (FX1 iPSC)

    Israel Weizmann Institute of Science (WIS)
    Disease:

    Fragile x syndrome

  6968. WISCi003-A (IPS(FORESKIN)-1)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6969. WISCi004-A (IPS(IMR90)-1)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6970. WISCi004-B (IPS(IMR90)-4 and WAi004-B)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6971. WISCi005-A (DS1 and UWWC1-DS1)

    United States University of Wisconsin (WISC)
    Disease:

    Trisomy 21

  6972. WISCi005-B (DS4 and UWWC1-DS4)

    United States University of Wisconsin (WISC)
    Disease:

    Trisomy 21

  6973. WISCi005-C (UWWC1-DS2U and DS2U)

    United States University of Wisconsin (WISC)
    Disease:

    Trisomy 21

  6974. WISCi006-A (2DS3 and UWWC1-2DS3)

    United States University of Wisconsin (WISC)
    Disease:

    Obsolete_down syndrome

  6975. WISCi007-A (WC026i-5807-3)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6976. WISCi007-B (WC027i-5807-5)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6977. WISCi007-C (WC028i-5807-6)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6978. WISCi008-A (WC029i-5907-1)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6979. WISCi008-B (WC030i-5907-2)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6980. WISCi008-C (WC031i-5907-6)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6981. WISCi009-A (WC032i-6007-1)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6982. WISCi009-B (WC033i-6007-2)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6983. WTSIi001-A (HPSI1213i-pahc_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6984. WTSIi001-B (HPSI1213i-pahc_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6985. WTSIi002-A (HPSI0913i-eika_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6986. WTSIi003-A (HPSI1213i-hehd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6987. WTSIi003-B (HPSI1213i-hehd_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6988. WTSIi004-A (HPSI1113i-qolg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6989. WTSIi004-B (HPSI1113i-qolg_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6990. WTSIi005-A (HPSI1113i-podx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6991. WTSIi005-B (HPSI1113i-podx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6992. WTSIi006-A (HPSI1113i-hayt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6993. WTSIi006-B (HPSI1113i-hayt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6994. WTSIi007-A (HPSI1113i-dons_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6995. WTSIi008-A (HPSI1013i-kuxp_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6996. WTSIi009-A (HPSI0913i-diku_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6997. WTSIi010-A (HPSI0314i-xugn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6998. WTSIi010-B (HPSI0314i-xugn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6999. WTSIi011-A (HPSI0314i-qonc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7000. WTSIi011-B (HPSI0314i-qonc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7001. WTSIi012-A (HPSI0314i-bubh_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7002. WTSIi012-B (HPSI0314i-bubh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7003. WTSIi013-A (HPSI0214i-kucg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7004. WTSIi014-A (HPSI0214i-heja_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7005. WTSIi014-B (HPSI0214i-heja_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7006. WTSIi015-A (HPSI0114i-rozh_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7007. WTSIi015-B (HPSI0114i-rozh_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7008. WTSIi016-A (HPSI0114i-oevr_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7009. WTSIi017-A (HPSI0114i-lexy_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7010. WTSIi017-B (HPSI0114i-lexy_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7011. WTSIi018-A (HPSI0114i-kolf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7012. WTSIi018-B (HPSI0114i-kolf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7013. WTSIi018-B-1 (HPSI0114i-kolf_2-C1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7014. WTSIi019-A (HPSI0114i-iisa_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7015. WTSIi019-B (HPSI0114i-iisa_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7016. WTSIi020-A (HPSI0114i-eipl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7017. WTSIi020-B (HPSI0114i-eipl_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7018. WTSIi021-A (HPSI1013i-wuye_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7019. WTSIi021-B (HPSI1013i-wuye_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7020. WTSIi022-A (HPSI1013i-yemz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7021. WTSIi022-B (HPSI1013i-yemz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7022. WTSIi023-A (HPSI0114i-zapk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7023. WTSIi023-B (HPSI0114i-zapk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7024. WTSIi024-A (HPSI0114i-vabj_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7025. WTSIi025-A (HPSI1013i-pamv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7026. WTSIi025-B (HPSI1013i-pamv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7027. WTSIi026-A (HPSI0314i-hoik_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7028. WTSIi027-A (HPSI0913i-oapg_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7029. WTSIi028-A (HPSI1213i-babk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7030. WTSIi029-A (HPSI1013i-garx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7031. WTSIi030-A (HPSI0214i-pelm_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7032. WTSIi030-B (HPSI0214i-pelm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7033. WTSIi031-A (HPSI0314i-bipt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7034. WTSIi032-A (HPSI1113i-bima_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7035. WTSIi032-B (HPSI1113i-bima_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7036. WTSIi033-A (HPSI1013i-aetc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7037. WTSIi034-A (HPSI0913i-kojv_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7038. WTSIi035-A (HPSI0913i-gooj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7039. WTSIi036-A (HPSI1113i-waus_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7040. WTSIi037-A (HPSI0114i-zoxy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7041. WTSIi038-A (HPSI1113i-ieki_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7042. WTSIi038-B (HPSI1113i-ieki_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7043. WTSIi039-A (HPSI1013i-wopl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7044. WTSIi040-A (HPSI0314i-qaqx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7045. WTSIi041-A (HPSI0114i-bezi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7046. WTSIi041-B (HPSI0114i-bezi_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7047. WTSIi042-A (HPSI1013i-jufd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7048. WTSIi042-B (HPSI1013i-jufd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7049. WTSIi044-A (HPSI0214i-eiwy_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7050. WTSIi045-A (HPSI0214i-heth_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7051. WTSIi046-A (HPSI0214i-wibj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7052. WTSIi046-B (HPSI0214i-wibj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7053. WTSIi047-A (HPSI0814i-bokz_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7054. WTSIi047-B (HPSI0814i-bokz_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7055. WTSIi048-A (HPSI0214i-datg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7056. WTSIi049-A (HPSI0514i-wiii_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7057. WTSIi049-B (HPSI0514i-wiii_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7058. WTSIi050-A (HPSI1014i-toss_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7059. WTSIi051-A (HPSI1113i-uofv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7060. WTSIi052-A (HPSI1114i-ziyn_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7061. WTSIi053-A (HPSI0413i-corn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7062. WTSIi054-A (HPSI0413i-nudd_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7063. WTSIi054-B (HPSI0413i-nudd_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7064. WTSIi055-A (HPSI0513i-debk_9)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7065. WTSIi055-B (HPSI0513i-debk_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7066. WTSIi056-A (HPSI0513i-dipe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7067. WTSIi057-A (HPSI0513i-giuf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7068. WTSIi057-B (HPSI0513i-giuf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7069. WTSIi058-A (HPSI0513i-suzg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7070. WTSIi059-A (HPSI0513i-uilw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7071. WTSIi060-A (HPSI0513i-veqz_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7072. WTSIi061-A (HPSI0513i-veve_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7073. WTSIi062-A (HPSI0513i-zaui_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7074. WTSIi063-A (HPSI0613i-aevs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7075. WTSIi064-A (HPSI0613i-bohf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7076. WTSIi065-A (HPSI0613i-eojr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7077. WTSIi065-B (HPSI0613i-eojr_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7078. WTSIi066-A (HPSI0613i-febc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7079. WTSIi066-B (HPSI0613i-febc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7080. WTSIi067-A (HPSI0713i-foop_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7081. WTSIi067-B (HPSI0713i-foop_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7082. WTSIi068-A (HPSI0613i-giuo_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7083. WTSIi068-B (HPSI0613i-giuo_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7084. WTSIi069-A (HPSI0613i-hegp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7085. WTSIi070-A (HPSI0713i-terl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7086. WTSIi070-B (HPSI0713i-terl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7087. WTSIi071-A (HPSI0913i-lise_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7088. WTSIi071-B (HPSI0913i-lise_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7089. WTSIi072-A (HPSI0114i-fikt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7090. WTSIi073-A (HPSI0314i-sojd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7091. WTSIi073-B (HPSI0314i-sojd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7092. WTSIi074-A (HPSI0114i-joxm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7093. WTSIi075-A (HPSI0114i-vass_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7094. WTSIi076-A (HPSI0214i-kehc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7095. WTSIi077-A (HPSI0314i-cuhk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7096. WTSIi077-B (HPSI0314i-cuhk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7097. WTSIi078-A (HPSI0314i-fafq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7098. WTSIi079-A (HPSI1013i-hiaf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7099. WTSIi079-B (HPSI1013i-hiaf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7100. WTSIi080-A (HPSI1013i-sebz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7101. WTSIi081-A (HPSI1113i-qorq_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7102. WTSIi081-B (HPSI1113i-qorq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7103. WTSIi082-A (HPSI1013i-cups_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7104. WTSIi083-A (HPSI1213i-xuja_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7105. WTSIi084-A (HPSI0713i-cicb_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7106. WTSIi084-B (HPSI0713i-cicb_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7107. WTSIi085-A (HPSI1113i-eofe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7108. WTSIi086-A (HPSI0913i-coyi_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7109. WTSIi087-A (HPSI0813i-uaqe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7110. WTSIi088-A (HPSI0913i-ruql_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7111. WTSIi089-A (HPSI0613i-xavk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7112. WTSIi089-B (HPSI0613i-xavk_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7113. WTSIi090-A (HPSI0813i-robp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7114. WTSIi091-A (HPSI0813i-ffdc_11)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7115. WTSIi091-B (HPSI0813i-ffdc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7116. WTSIi092-A (HPSI0713i-nemb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7117. WTSIi093-A (HPSI0413i-sukz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7118. WTSIi094-A (HPSI0613i-xucm_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7119. WTSIi095-A (HPSI0813i-vajx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7120. WTSIi096-A (HPSI0813i-guss_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7121. WTSIi097-A (HPSI0813i-aizi_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7122. WTSIi097-B (HPSI0813i-aizi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7123. WTSIi098-A (HPSI1213i-nekd_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7124. WTSIi099-A (HPSI0813i-civh_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7125. WTSIi099-B (HPSI0813i-civh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7126. WTSIi100-A (HPSI0813i-zexw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7127. WTSIi101-A (HPSI0513i-fejf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7128. WTSIi102-A (HPSI0413i-iakz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7129. WTSIi102-B (HPSI0413i-iakz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7130. WTSIi103-A (HPSI1213i-nusw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7131. WTSIi104-A (HPSI0513i-coio_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7132. WTSIi104-B (HPSI0513i-coio_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7133. WTSIi105-A (HPSI0313i-airc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7134. WTSIi105-B (HPSI0313i-airc_66)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7135. WTSIi105-D (HPSI0313i-airc_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7136. WTSIi106-A (HPSI0613i-hikj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7137. WTSIi106-B (HPSI0613i-hikj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7138. WTSIi107-A (HPSI0813i-iill_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7139. WTSIi107-B (HPSI0813i-iill_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7140. WTSIi108-A (HPSI0313i-cesj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7141. WTSIi109-A (HPSI0413i-coxy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7142. WTSIi109-B (HPSI0413i-coxy_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7143. WTSIi110-A (HPSI0713i-darw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7144. WTSIi110-B (HPSI0713i-darw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7145. WTSIi111-A (HPSI0513i-euir_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7146. WTSIi111-B (HPSI0513i-euir_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7147. WTSIi112-A (HPSI0613i-funp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7148. WTSIi112-B (HPSI0613i-funp_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7149. WTSIi113-A (HPSI0913i-gedo_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7150. WTSIi113-B (HPSI0913i-gedo_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7151. WTSIi114-A (HPSI0513i-golb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7152. WTSIi115-A (HPSI0513i-iasn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7153. WTSIi116-A (HPSI0813i-iicq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7154. WTSIi116-B (HPSI0813i-iicq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7155. WTSIi117-A (HPSI0613i-liun_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7156. WTSIi117-B (HPSI0613i-liun_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7157. WTSIi118-A (HPSI0813i-meqo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7158. WTSIi118-B (HPSI0813i-meqo_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7159. WTSIi119-A (HPSI0613i-oefg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7160. WTSIi120-A (HPSI0513i-oeoo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7161. WTSIi121-A (HPSI0413i-ougl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7162. WTSIi121-B (HPSI0413i-ougl_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7163. WTSIi122-A (HPSI0413i-peop_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7164. WTSIi122-B (HPSI0413i-peop_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7165. WTSIi123-A (HPSI0713i-qimz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7166. WTSIi123-B (HPSI0713i-qimz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7167. WTSIi124-A (HPSI0713i-ruyv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7168. WTSIi124-B (HPSI0713i-ruyv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7169. WTSIi125-A (HPSI0413i-uahf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7170. WTSIi126-A (HPSI0913i-vopm_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7171. WTSIi127-A (HPSI0413i-xekf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7172. WTSIi128-A (HPSI0413i-yuze_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7173. WTSIi129-A (HPSI0613i-zisa_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7174. WTSIi129-B (HPSI0613i-zisa_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7175. WTSIi130-A (HPSI0713i-aehn_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7176. WTSIi130-B (HPSI0713i-aehn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7177. WTSIi131-A (HPSI0513i-aipt_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7178. WTSIi131-B (HPSI0513i-aipt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7179. WTSIi132-A (HPSI0613i-bawa_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7180. WTSIi133-A (HPSI0713i-dard_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7181. WTSIi133-B (HPSI0713i-dard_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7182. WTSIi134-A (HPSI0513i-dulv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7183. WTSIi134-B (HPSI0513i-dulv_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7184. WTSIi135-A (HPSI0214i-feec_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7185. WTSIi135-B (HPSI0214i-feec_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7186. WTSIi136-A (HPSI0913i-iuqb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7187. WTSIi137-A (HPSI0613i-lizq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7188. WTSIi137-B (HPSI0613i-lizq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7189. WTSIi138-A (HPSI0414i-mita_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7190. WTSIi139-A (HPSI1113i-oaaz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7191. WTSIi139-B (HPSI1113i-oaaz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7192. WTSIi140-A (HPSI0613i-oomz_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7193. WTSIi140-B (HPSI0613i-oomz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7194. WTSIi141-A (HPSI0613i-qanu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7195. WTSIi141-B (HPSI0613i-qanu_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7196. WTSIi142-A (HPSI0613i-qony_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7197. WTSIi142-B (HPSI0613i-qony_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7198. WTSIi143-A (HPSI0214i-rayr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7199. WTSIi144-A (HPSI0114i-wegi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7200. WTSIi145-A (HPSI0813i-wots_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7201. WTSIi146-A (HPSI0613i-xosg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7202. WTSIi147-A (HPSI1013i-mijn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7203. WTSIi148-A (HPSI0114i-veui_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7204. WTSIi149-A (HPSI0913i-laia_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7205. WTSIi150-A (HPSI0414i-jetz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7206. WTSIi151-A (HPSI0414i-fixm_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7207. WTSIi152-A (HPSI0414i-eafb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7208. WTSIi153-A (HPSI0414i-puvg_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7209. WTSIi154-A (HPSI0414i-lavd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7210. WTSIi155-A (HPSI0414i-hutq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7211. WTSIi156-A (HPSI0414i-xugr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7212. WTSIi157-A (HPSI0614i-eavo_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7213. WTSIi158-A (HPSI0914i-fuhz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7214. WTSIi159-A (HPSI0714i-gibe_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7215. WTSIi160-A (HPSI0914i-verf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7216. WTSIi161-A (HPSI0714i-rajk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7217. WTSIi162-A (HPSI0914i-lopq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7218. WTSIi163-A (HPSI1014i-suok_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7219. WTSIi164-A (HPSI0614i-foyj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7220. WTSIi165-A (HPSI0414i-reng_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7221. WTSIi166-A (HPSI0414i-wize_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7222. WTSIi167-A (HPSI1013i-funy_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7223. WTSIi168-A (HPSI0214i-poih_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7224. WTSIi168-B (HPSI0214i-poih_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7225. WTSIi169-A (HPSI0614i-miaj_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7226. WTSIi169-B (HPSI0614i-miaj_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7227. WTSIi170-A (HPSI1213i-tolg_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7228. WTSIi170-B (HPSI1213i-tolg_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7229. WTSIi171-A (HPSI0914i-zerv_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7230. WTSIi171-B (HPSI0914i-zerv_8)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7231. WTSIi172-A (HPSI0914i-laey_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7232. WTSIi172-B (HPSI0914i-laey_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7233. WTSIi173-A (HPSI0414i-naju_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7234. WTSIi174-A (HPSI0614i-paab_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7235. WTSIi174-B (HPSI0614i-paab_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7236. WTSIi175-A (HPSI1014i-tixi_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7237. WTSIi176-A (HPSI0714i-iudw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7238. WTSIi176-B (HPSI0714i-iudw_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7239. WTSIi177-A (HPSI0414i-xojn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7240. WTSIi178-A (HPSI0215i-fawm_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7241. WTSIi178-B (HPSI0215i-fawm_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7242. WTSIi179-A (HPSI0314i-wigw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7243. WTSIi180-A (HPSI0514i-puie_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7244. WTSIi180-B (HPSI0514i-puie_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7245. WTSIi181-A (HPSI0514i-rutc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7246. WTSIi182-A (HPSI0614i-kegd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7247. WTSIi183-A (HPSI0414i-oaqd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7248. WTSIi183-B (HPSI0414i-oaqd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7249. WTSIi184-A (HPSI1014i-qayj_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7250. WTSIi184-B (HPSI1014i-qayj_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7251. WTSIi185-A (HPSI0414i-seru_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7252. WTSIi185-B (HPSI0414i-seru_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7253. WTSIi186-A (HPSI1014i-babz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7254. WTSIi187-A (HPSI1013i-sita_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7255. WTSIi188-A (HPSI1014i-kefb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7256. WTSIi189-A (HPSI1014i-quls_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7257. WTSIi190-A (HPSI0914i-kajh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7258. WTSIi190-B (HPSI0914i-kajh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7259. WTSIi191-A (HPSI0215i-oilg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7260. WTSIi191-B (HPSI0215i-oilg_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7261. WTSIi192-A (HPSI0414i-biiw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7262. WTSIi193-A (HPSI0414i-cekz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7263. WTSIi194-A (HPSI0614i-dixh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7264. WTSIi195-A (HPSI0414i-eevy_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7265. WTSIi195-B (HPSI0414i-eevy_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7266. WTSIi196-A (HPSI0514i-eoxi_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7267. WTSIi197-A (HPSI0714i-fasu_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7268. WTSIi198-A (HPSI0414i-fuai_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7269. WTSIi199-A (HPSI0614i-guyj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7270. WTSIi200-A (HPSI0414i-kefk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7271. WTSIi201-A (HPSI0614i-koqx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7272. WTSIi202-A (HPSI0714i-oebj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7273. WTSIi203-A (HPSI0714i-oojs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7274. WTSIi204-A (HPSI0414i-oulr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7275. WTSIi204-B (HPSI0414i-oulr_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7276. WTSIi205-A (HPSI0514i-pulk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7277. WTSIi206-A (HPSI0813i-fpdk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7278. WTSIi207-A (HPSI0813i-ffdr_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7279. WTSIi208-A (HPSI0513i-kesz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7280. WTSIi208-B (HPSI0513i-kesz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7281. WTSIi209-A (HPSI0613i-dium_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7282. WTSIi211-A (HPSI0513i-huls_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7283. WTSIi212-A (HPSI0613i-auim_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7284. WTSIi212-B (HPSI0613i-auim_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7285. WTSIi213-A (HPSI0713i-kaks_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7286. WTSIi213-B (HPSI0713i-kaks_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7287. WTSIi214-A (HPSI0513i-leeh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7288. WTSIi214-B (HPSI0513i-leeh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7289. WTSIi216-A (HPSI0613i-riiv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7290. WTSIi216-B (HPSI0613i-riiv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7291. WTSIi217-A (HPSI0513i-cuau_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7292. WTSIi217-B (HPSI0513i-cuau_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7293. WTSIi218-A (HPSI0914i-euts_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7294. WTSIi219-A (HPSI0613i-jorr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7295. WTSIi222-A (HPSI0613i-vorx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7296. WTSIi222-B (HPSI0613i-vorx_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7297. WTSIi223-A (HPSI0813i-piun_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7298. WTSIi225-A (HPSI0513i-xegx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7299. WTSIi225-B (HPSI0513i-xegx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7300. WTSIi227-A (HPSI1113i-wetu_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7301. WTSIi228-A (HPSI0514i-qihv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7302. WTSIi232-A (HPSI0613i-focm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7303. WTSIi233-A (HPSI0513i-cehw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7304. WTSIi235-A (HPSI0513i-uoxz_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7305. WTSIi235-B (HPSI0513i-uoxz_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7306. WTSIi236-A (HPSI0813i-voas_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7307. WTSIi238-A (HPSI0914i-suop_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7308. WTSIi238-B (HPSI0914i-suop_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7309. WTSIi241-A (HPSI0913i-lofv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7310. WTSIi241-B (HPSI0913i-lofv_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7311. WTSIi243-A (HPSI0414i-ceik_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7312. WTSIi243-B (HPSI0414i-ceik_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7313. WTSIi245-A (HPSI0714i-keui_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7314. WTSIi245-B (HPSI0714i-keui_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7315. WTSIi247-A (HPSI0614i-oicx_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7316. WTSIi247-B (HPSI0614i-oicx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7317. WTSIi248-A (HPSI0213i-koun_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7318. WTSIi248-B (HPSI0213i-koun_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7319. WTSIi249-A (HPSI0614i-uilk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7320. WTSIi249-B (HPSI0614i-uilk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7321. WTSIi250-A (HPSI0115i-melw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7322. WTSIi250-B (HPSI0115i-melw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7323. WTSIi252-A (HPSI0115i-vazt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7324. WTSIi252-B (HPSI0115i-vazt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7325. WTSIi253-A (HPSI0514i-letw_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7326. WTSIi253-B (HPSI0514i-letw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7327. WTSIi254-A (HPSI0914i-jejf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7328. WTSIi254-B (HPSI0914i-jejf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7329. WTSIi255-A (HPSI0115i-aion_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7330. WTSIi255-B (HPSI0115i-aion_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7331. WTSIi256-A (HPSI1014i-tuju_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7332. WTSIi256-B (HPSI1014i-tuju_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7333. WTSIi257-A (HPSI0714i-burb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7334. WTSIi257-B (HPSI0714i-burb_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7335. WTSIi258-A (HPSI0913i-bulb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7336. WTSIi259-A (HPSI0514i-vuna_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7337. WTSIi260-A (HPSI0414i-oikd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7338. WTSIi260-B (HPSI0414i-oikd_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7339. WTSIi261-A (HPSI1113i-wahn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7340. WTSIi261-B (HPSI1113i-wahn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7341. WTSIi262-A (HPSI0514i-sohd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7342. WTSIi262-B (HPSI0514i-sohd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7343. WTSIi263-A (HPSI0614i-lepk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7344. WTSIi263-B (HPSI0614i-lepk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7345. WTSIi265-A (HPSI0714i-pipw_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7346. WTSIi265-B (HPSI0714i-pipw_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7347. WTSIi266-A (HPSI0115i-gifk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7348. WTSIi267-A (HPSI0115i-iiyk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7349. WTSIi267-B (HPSI0115i-iiyk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7350. WTSIi268-A (HPSI0714i-nufh_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7351. WTSIi268-B (HPSI0714i-nufh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7352. WTSIi269-A (HPSI0115i-hecn_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7353. WTSIi269-B (HPSI0115i-hecn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7354. WTSIi270-A (HPSI0514i-fiaj_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7355. WTSIi270-B (HPSI0514i-fiaj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7356. WTSIi271-A (HPSI0414i-gesg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7357. WTSIi274-A (HPSI0714i-jilk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7358. WTSIi274-B (HPSI0714i-jilk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7359. WTSIi275-A (HPSI0115i-uolo_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7360. WTSIi276-A (HPSI1014i-juuy_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7361. WTSIi277-A (HPSI1114i-ualf_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7362. WTSIi277-B (HPSI1114i-ualf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7363. WTSIi279-A (HPSI0813i-ffdj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7364. WTSIi281-A (HPSI0115i-qoog_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7365. WTSIi281-B (HPSI0115i-qoog_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7366. WTSIi283-A (HPSI0514i-toco_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7367. WTSIi284-A (HPSI0614i-liqa_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7368. WTSIi284-B (HPSI0614i-liqa_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7369. WTSIi285-A (HPSI0414i-sebn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7370. WTSIi285-B (HPSI0414i-sebn_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7371. WTSIi287-A (HPSI0514i-lako_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7372. WTSIi287-B (HPSI0514i-lako_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7373. WTSIi288-A (HPSI0715i-meue_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7374. WTSIi288-B (HPSI0715i-meue_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7375. WTSIi291-A (HPSI0215i-yoch_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7376. WTSIi293-A (HPSI0215i-deyz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7377. WTSIi293-B (HPSI0215i-deyz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7378. WTSIi294-A (HPSI1014i-bilx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7379. WTSIi294-B (HPSI1014i-bilx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7380. WTSIi296-A (HPSI0214i-giju_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7381. WTSIi296-B (HPSI0214i-giju_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7382. WTSIi297-A (HPSI0813i-fpdl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7383. WTSIi297-B (HPSI1213i-foqj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7384. WTSIi297-C (HPSI0913i-ffdl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7385. WTSIi297-D (HPSI0813i-fpdl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7386. WTSIi299-A (HPSI0213i-nawk_55)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7387. WTSIi300-A (HPSI0714i-kute_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7388. WTSIi300-B (HPSI0714i-kute_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7389. WTSIi302-A (HPSI1014i-nosn_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7390. WTSIi302-B (HPSI1014i-nosn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7391. WTSIi303-A (HPSI0914i-qehq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7392. WTSIi303-B (HPSI0914i-qehq_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7393. WTSIi308-A (HPSI0115i-zihe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7394. WTSIi310-A (HPSI0614i-ciwj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7395. WTSIi310-B (HPSI0614i-ciwj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7396. WTSIi311-A (HPSI0215i-hipn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7397. WTSIi311-B (HPSI0215i-hipn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7398. WTSIi316-A (HPSI0514i-kuco_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7399. WTSIi316-B (HPSI0514i-kuco_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7400. WTSIi317-A (HPSI1014i-eesb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7401. WTSIi318-A (HPSI1014i-sehl_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7402. WTSIi322-A (HPSI0514i-naah_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7403. WTSIi322-B (HPSI0514i-naah_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7404. WTSIi327-A (HPSI0715i-zaie_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7405. WTSIi327-B (HPSI0715i-zaie_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7406. WTSIi341-A (HPSI1014i-riun_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7407. WTSIi342-A (HPSI0613i-ueah_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7408. WTSIi342-B (HPSI0613i-ueah_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7409. WTSIi345-A (HPSI0715i-aowh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7410. WTSIi347-A (HPSI0814i-doao_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7411. WTSIi347-B (HPSI0814i-doao_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7412. WTSIi349-A (HPSI0914i-gine_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7413. WTSIi350-A (HPSI0513i-momt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7414. WTSIi351-A (HPSI0513i-oibg_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7415. WTSIi353-A (HPSI0914i-ouvb_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7416. WTSIi354-A (HPSI0513i-netf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7417. WTSIi355-A (HPSI0413i-yotv_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7418. WTSIi355-B (HPSI0413i-yotv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7419. WTSIi357-A (HPSI0713i-wiol_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7420. WTSIi362-A (HPSI0513i-oarz_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7421. WTSIi362-B (HPSI0513i-oarz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7422. WTSIi363-A (HPSI1014i-vils_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7423. WTSIi364-A (HPSI1013i-zagm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7424. WTSIi365-A (HPSI0514i-yelp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7425. WTSIi368-A (HPSI0914i-iezw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7426. WTSIi369-A (HPSI0514i-uenn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7427. WTSIi370-A (HPSI0613i-nukw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7428. WTSIi373-A (HPSI1013i-jogf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7429. WTSIi374-A (HPSI1014i-roug_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7430. WTSIi376-A (HPSI0713i-uimo_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7431. WTSIi377-A (HPSI0713i-veku_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7432. WTSIi378-A (HPSI0713i-nocf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7433. WTSIi380-A (HPSI0713i-pusf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7434. WTSIi382-A (HPSI0614i-denw_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7435. WTSIi385-A (HPSI0713i-fett_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7436. WTSIi387-A (HPSI0513i-dovq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7437. WTSIi388-A (HPSI0115i-paim_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7438. WTSIi388-B (HPSI0115i-paim_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7439. WTSIi389-A (HPSI0614i-voce_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7440. WTSIi389-B (HPSI0614i-voce_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7441. WTSIi390-A (HPSI1113i-hajc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7442. WTSIi392-A (HPSI0513i-sucd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7443. WTSIi394-A (HPSI0914i-vaka_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7444. WTSIi396-A (HPSI0414i-kodf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7445. WTSIi398-A (HPSI0414i-rauj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7446. WTSIi399-A (HPSI0614i-gawh_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7447. WTSIi399-B (HPSI0614i-gawh_12)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7448. WTSIi400-A (HPSI0414i-tout_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7449. WTSIi401-A (HPSI0714i-meet_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7450. WTSIi402-A (HPSI0714i-ouzk_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7451. WTSIi402-B (HPSI0714i-ouzk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7452. WTSIi403-A (HPSI0913i-rufg_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7453. WTSIi403-B (HPSI0913i-rufg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7454. WTSIi405-A (HPSI0614i-fovu_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7455. WTSIi405-B (HPSI0614i-fovu_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7456. WTSIi406-A (HPSI0614i-mesr_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7457. WTSIi407-A (HPSI0914i-hidy_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7458. WTSIi407-B (HPSI0914i-hidy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7459. WTSIi408-A (HPSI0414i-niim_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7460. WTSIi408-B (HPSI0414i-niim_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7461. WTSIi409-A (HPSI0414i-walu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7462. WTSIi410-A (HPSI0614i-zoio_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7463. WTSIi410-B (HPSI0614i-zoio_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7464. WTSIi411-A (HPSI0914i-rejf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7465. WTSIi412-A (HPSI0614i-wihj_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7466. WTSIi412-B (HPSI0614i-wihj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7467. WTSIi414-A (HPSI0614i-eisk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7468. WTSIi414-B (HPSI0614i-eisk_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7469. WTSIi415-A (HPSI0614i-laig_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7470. WTSIi415-B (HPSI0614i-laig_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7471. WTSIi416-A (HPSI0514i-aomr_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7472. WTSIi416-B (HPSI0514i-aomr_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7473. WTSIi417-A (HPSI0614i-voxu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7474. WTSIi417-B (HPSI0614i-voxu_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7475. WTSIi419-A (HPSI0514i-kidt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7476. WTSIi420-A (HPSI0914i-tifo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7477. WTSIi420-B (HPSI0914i-tifo_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7478. WTSIi422-A (HPSI0414i-zazi_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7479. WTSIi422-B (HPSI0414i-zazi_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7480. WTSIi424-A (HPSI0514i-mure_9)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7481. WTSIi424-B (HPSI0514i-mure_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7482. WTSIi426-A (HPSI0714i-mejk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7483. WTSIi428-A (HPSI0714i-lutt_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7484. WTSIi430-A (HPSI0514i-aecv_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7485. WTSIi430-B (HPSI0514i-aecv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7486. WTSIi431-A (HPSI0514i-tavh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7487. WTSIi436-A (HPSI0714i-zaos_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7488. WTSIi438-A (HPSI0714i-pirs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7489. WTSIi439-A (HPSI0714i-mitg_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7490. WTSIi444-A (HPSI0714i-riya_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7491. WTSIi445-A (HPSI0714i-xebt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7492. WTSIi446-A (HPSI1113i-vuud_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7493. WTSIi447-A (HPSI0416i-zige_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7494. WTSIi447-B (HPSI0416i-zige_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7495. WTSIi448-A (HPSI0316i-muwv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7496. WTSIi448-B (HPSI0316i-muwv_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7497. WTSIi450-A (HPSI0216i-aiid_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7498. WTSIi450-B (HPSI0216i-aiid_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7499. WTSIi452-A (HPSI0115i-xaka_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7500. WTSIi452-B (HPSI0115i-xaka_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7501. WTSIi453-A (HPSI0416i-fiwt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7502. WTSIi454-A (HPSI0516i-iool_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7503. WTSIi454-B (HPSI0516i-iool_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7504. WTSIi455-A (HPSI0516i-eosr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7505. WTSIi456-A (HPSI0616i-kulz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7506. WTSIi456-B (HPSI0616i-kulz_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7507. WTSIi457-A (HPSI0115i-iinu_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7508. WTSIi457-B (HPSI0115i-iinu_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7509. WTSIi458-A (HPSI0614i-lipl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7510. WTSIi458-B (HPSI0614i-lipl_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7511. WTSIi459-A (HPSI0516i-zukb_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7512. WTSIi459-B (HPSI0516i-zukb_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7513. WTSIi460-A (HPSI0516i-jepf_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7514. WTSIi460-B (HPSI0516i-jepf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7515. WTSIi461-A (HPSI0316i-eoko_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7516. WTSIi461-B (HPSI0316i-eoko_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7517. WTSIi462-A (HPSI0316i-miov_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7518. WTSIi463-A (HPSI0716i-yibs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7519. WTSIi463-B (HPSI0716i-yibs_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7520. WTSIi464-A (HPSI0516i-eitu_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7521. WTSIi464-B (HPSI0516i-eitu_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7522. WTSIi465-A (HPSI0714i-xiry_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7523. WTSIi465-B (HPSI0714i-xiry_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7524. WTSIi466-A (HPSI0416i-aicq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7525. WTSIi466-B (HPSI0416i-aicq_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7526. WTSIi467-A (HPSI0513i-bicb_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7527. WTSIi468-A (HPSI1013i-woci_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7528. WTSIi469-A (HPSI0316i-ierp_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7529. WTSIi470-A (HPSI0516i-jory_9)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7530. WTSIi470-B (HPSI0516i-jory_10)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7531. WTSIi472-A (HPSI0216i-vieg_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7532. WTSIi472-B (HPSI0216i-vieg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7533. WTSIi473-A (HPSI0813i-mioj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7534. WTSIi473-B (HPSI0813i-mioj_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7535. WTSIi474-A (HPSI0216i-dewh_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7536. WTSIi474-B (HPSI0216i-dewh_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7537. WTSIi475-A (HPSI0514i-qajt_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7538. WTSIi475-B (HPSI0514i-qajt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7539. WTSIi476-A (HPSI0813i-peoj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7540. WTSIi477-A (HPSI0514i-kooz_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7541. WTSIi478-A (HPSI0414i-nolz_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7542. WTSIi479-A (HPSI0616i-beyk_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7543. WTSIi479-B (HPSI0616i-beyk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7544. WTSIi480-A (HPSI0516i-iuoc_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7545. WTSIi480-B (HPSI0516i-iuoc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7546. WTSIi481-A (HPSI0716i-toba_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7547. WTSIi482-A (HPSI0616i-gayk_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7548. WTSIi482-B (HPSI0616i-gayk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7549. WTSIi483-A (HPSI0416i-ourj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7550. WTSIi483-B (HPSI0416i-ourj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7551. WTSIi484-A (HPSI0716i-bakv_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7552. WTSIi484-B (HPSI0716i-bakv_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7553. WTSIi485-A (HPSI0614i-kecw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7554. WTSIi485-B (HPSI0614i-kecw_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7555. WTSIi486-A (HPSI0516i-hapz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7556. WTSIi486-B (HPSI0516i-hapz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7557. WTSIi487-A (HPSI0516i-goek_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7558. WTSIi488-A (HPSI0516i-oazw_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7559. WTSIi488-B (HPSI0516i-oazw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7560. WTSIi493-A (HPSI0416i-ruah_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7561. WTSIi493-B (HPSI0416i-ruah_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7562. WTSIi495-A (HPSI0314i-kujn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7563. WTSIi495-B (HPSI0314i-kujn_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7564. WTSIi496-A (HPSI0516i-yibc_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7565. WTSIi497-A (HPSI0616i-oajt_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7566. WTSIi497-B (HPSI0616i-oajt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7567. WTSIi498-A (HPSI0616i-biln_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7568. WTSIi498-B (HPSI0616i-biln_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7569. WTSIi499-A (HPSI0416i-xutl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7570. WTSIi501-A (HPSI0316i-circ_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7571. WTSIi501-B (HPSI0316i-circ_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7572. WTSIi502-A (HPSI0216i-boho_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7573. WTSIi503-A (HPSI0416i-mapx_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7574. WTSIi503-B (HPSI0416i-mapx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7575. WTSIi506-A (HPSI0616i-giql_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7576. WTSIi506-B (HPSI0616i-giql_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7577. WTSIi507-A (HPSI0614i-uevq_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7578. WTSIi507-B (HPSI0614i-uevq_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7579. WTSIi508-A (HPSI0416i-jewl_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7580. WTSIi508-B (HPSI0416i-jewl_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7581. WTSIi509-A (HPSI0416i-ourj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7582. WTSIi510-A (HPSI0216i-xanu_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7583. WTSIi510-B (HPSI0216i-xanu_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7584. WTSIi512-A (HPSI0416i-ruah_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7585. WTSIi514-A (HPSI0416i-iooi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7586. WTSIi514-B (HPSI0416i-iooi_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7587. WTSIi515-A (HPSI0416i-bife_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7588. WTSIi516-A (HPSI0216i-iogu_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7589. WTSIi516-B (HPSI0216i-iogu_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7590. WTSIi518-A (HPSI0416i-cihd_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7591. WTSIi519-A (HPSI0416i-sevr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7592. WTSIi519-B (HPSI0416i-sevr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7593. WTSIi522-A (HPSI0516i-pews_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7594. WTSIi522-B (HPSI0516i-pews_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7595. WTSIi524-A (HPSI0616i-xuvy_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7596. WTSIi525-A (HPSI0616i-bury_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7597. WTSIi525-B (HPSI0616i-bury_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7598. WTSIi526-A (HPSI0316i-qeti_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7599. WTSIi526-B (HPSI0316i-qeti_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7600. WTSIi527-A (HPSI0216i-heub_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7601. WTSIi527-B (HPSI0216i-heub_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7602. WTSIi529-A (HPSI0716i-yipp_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7603. WTSIi529-B (HPSI0716i-yipp_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7604. WTSIi530-A (HPSI0215i-zett_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7605. WTSIi531-A (HPSI0616i-kayf_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7606. WTSIi531-B (HPSI0616i-kayf_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7607. WTSIi534-A (HPSI0616i-eomr_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7608. WTSIi545-A (HPSI0416i-eapo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7609. WTSIi548-A (HPSI0416i-mefc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7610. WTSIi548-B (HPSI0416i-mefc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7611. WTSIi554-A (HPSI0216i-dacv_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7612. WTSIi555-A (HPSI0316i-xaqm_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Congenital hyperinsulinism

  7613. WTSIi558-A (HPSI0516i-oadp_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7614. WTSIi558-B (HPSI0516i-oadp_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7615. WTSIi560-A (HPSI0214i-bute_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7616. WTSIi561-A (HPSI0813i-aomg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7617. WTSIi563-A (HPSI0516i-zujs_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7618. WTSIi564-A (HPSI0313i-fecs_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7619. WTSIi565-A (HPSI0313i-xovo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7620. WTSIi567-A (HPSI0813i-eiqh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7621. WTSIi568-A (HPSI0216i-rihx_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7622. WTSIi569-A (HPSI0613i-qonr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7623. WTSIi569-B (HPSI0613i-qonr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7624. WTSIi570-A (HPSI0213i-koun_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7625. WTSIi571-A (HPSI0513i-pedc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7626. WTSIi573-A (HPSI0115i-qaqp_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7627. WTSIi573-B (HPSI0115i-qaqp_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7628. WTSIi576-A (HPSI0216i-feht_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7629. WTSIi580-A (HPSI0316i-aask_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7630. WTSIi582-A (HPSI0613i-oesx_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7631. WTSIi590-A (HPSI0115i-gost_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7632. WTSIi591-A (HPSI0514i-oupf_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7633. WTSIi591-B (HPSI0514i-oupf_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7634. WTSIi593-A (HPSI0514i-tert_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7635. WTSIi593-B (HPSI0514i-tert_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7636. WTSIi594-A (HPSI0115i-aoxv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7637. WTSIi594-B (HPSI0115i-aoxv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7638. WTSIi595-A (HPSI0814i-siqu_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7639. WTSIi595-B (HPSI0814i-siqu_11)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7640. WTSIi596-A (HPSI0514i-oekw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7641. WTSIi597-A (HPSI0414i-uawq_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7642. WTSIi598-A (HPSI1114i-kuul_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7643. WTSIi598-B (HPSI1114i-kuul_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7644. WTSIi599-A (HPSI0614i-lirf_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7645. WTSIi599-B (HPSI0614i-lirf_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7646. WTSIi602-A (HPSI0614i-puhk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7647. WTSIi602-B (HPSI0614i-puhk_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7648. WTSIi603-A (HPSI0614i-qunz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7649. WTSIi603-B (HPSI0614i-qunz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7650. WTSIi607-A (HPSI1014i-xiyh_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7651. WTSIi607-B (HPSI1014i-xiyh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7652. WTSIi609-A (HPSI0516i-suqd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7653. WTSIi609-B (HPSI0516i-suqd_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7654. WTSIi610-A (HPSI1116i-naum_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7655. WTSIi611-A (HPSI0816i-neow_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7656. WTSIi611-B (HPSI0816i-neow_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7657. WTSIi612-A (HPSI0616i-mifg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7658. WTSIi612-B (HPSI0616i-mifg_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7659. WTSIi613-A (HPSI1116i-rafd_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7660. WTSIi613-B (HPSI1116i-rafd_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7661. WTSIi614-A (HPSI0616i-rily_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7662. WTSIi614-B (HPSI0616i-rily_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7663. WTSIi615-A (HPSI0115i-rakq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7664. WTSIi615-B (HPSI0115i-rakq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7665. WTSIi617-A (HPSI0215i-uiao_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7666. WTSIi617-B (HPSI0215i-uiao_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7667. WTSIi618-A (HPSI1114i-xiby_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7668. WTSIi618-B (HPSI1114i-xiby_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7669. WTSIi619-A (HPSI0115i-kozf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7670. WTSIi619-B (HPSI0115i-kozf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7671. WTSIi620-A (HPSI0616i-uegn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7672. WTSIi620-B (HPSI0616i-uegn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7673. WTSIi621-A (HPSI0916i-vorn_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7674. WTSIi621-B (HPSI0916i-vorn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7675. WTSIi622-A (HPSI0516i-menz_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7676. WTSIi622-B (HPSI0516i-menz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7677. WTSIi623-A (HPSI0516i-yist_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7678. WTSIi623-B (HPSI0516i-yist_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7679. WTSIi624-A (HPSI0616i-uofs_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7680. WTSIi624-B (HPSI0616i-uofs_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7681. WTSIi626-A (HPSI0914i-yuvg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7682. WTSIi627-A (HPSI0414i-voqc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7683. WTSIi632-A (HPSI0316i-vats_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7684. WTSIi632-B (HPSI0316i-vats_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7685. WTSIi633-A (HPSI0714i-oatm_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7686. WTSIi633-B (HPSI0714i-oatm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7687. WTSIi634-A (HPSI0115i-timk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7688. WTSIi635-A (HPSI0414i-zabk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  7689. WTSIi636-A (HPSI0514i-yewo_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7690. WTSIi638-A (HPSI0916i-zipi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7691. WTSIi638-B (HPSI0916i-zipi_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7692. WTSIi641-A (HPSI0516i-aaun_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7693. WTSIi641-B (HPSI0516i-aaun_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7694. WTSIi643-A (HPSI0514i-suul_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7695. WTSIi643-B (HPSI0514i-suul_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7696. WTSIi644-A (HPSI0115i-sehp_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7697. WTSIi644-B (HPSI0115i-sehp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7698. WTSIi645-A (HPSI0514i-xufp_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7699. WTSIi646-A (HPSI1114i-zuuy_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7700. WTSIi646-B (HPSI1114i-zuuy_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7701. WTSIi648-A (HPSI0616i-mesv_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7702. WTSIi648-B (HPSI0616i-mesv_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7703. WTSIi654-A (HPSI0115i-uupc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7704. WTSIi657-A (HPSI0916i-moyn_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7705. WTSIi657-B (HPSI0916i-moyn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7706. WTSIi658-A (HPSI0816i-fuuy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7707. WTSIi659-A (HPSI1116i-wakr_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7708. WTSIi659-B (HPSI1116i-wakr_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7709. WTSIi660-A (HPSI0115i-tiku_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7710. WTSIi660-B (HPSI0115i-tiku_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7711. WTSIi661-A (HPSI0614i-xubw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7712. WTSIi661-B (HPSI0614i-xubw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7713. WTSIi662-A (HPSI1116i-mebq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7714. WTSIi662-B (HPSI1116i-mebq_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7715. WTSIi665-A (HPSI0616i-euia_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7716. WTSIi666-A (HPSI0514i-xayd_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7717. WTSIi666-B (HPSI0514i-xayd_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7718. WTSIi669-A (HPSI0816i-aorf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7719. WTSIi669-B (HPSI0816i-aorf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7720. WTSIi670-A (HPSI0614i-juzt_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7721. WTSIi672-A (HPSI0516i-quqp_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7722. WTSIi672-B (HPSI0516i-quqp_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7723. WTSIi673-A (HPSI0616i-vaqx_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7724. WTSIi673-B (HPSI0616i-vaqx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7725. WTSIi674-A (HPSI1116i-vozo_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7726. WTSIi674-B (HPSI1116i-vozo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7727. WTSIi675-A (HPSI0616i-iuse_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7728. WTSIi675-B (HPSI0616i-iuse_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7729. WTSIi676-A (HPSI0616i-heba_11)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7730. WTSIi676-B (HPSI0616i-heba_9)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7731. WTSIi679-A (HPSI0316i-ponl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7732. WTSIi679-B (HPSI0316i-ponl_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7733. WTSIi680-A (HPSI0516i-peoo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7734. WTSIi680-B (HPSI0516i-peoo_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7735. WTSIi685-A (HPSI0416i-ioys_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7736. WTSIi685-B (HPSI0416i-ioys_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7737. WTSIi686-A (HPSI0616i-baxr_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7738. WTSIi686-B (HPSI0616i-baxr_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7739. WTSIi687-A (HPSI0916i-vajy_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7740. WTSIi687-B (HPSI0916i-vajy_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7741. WTSIi688-A (HPSI1116i-wiau_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7742. WTSIi688-B (HPSI1116i-wiau_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7743. WTSIi689-A (HPSI0616i-newl_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7744. WTSIi690-A (HPSI0115i-jotn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7745. WTSIi690-B (HPSI0115i-jotn_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7746. WTSIi691-A (HPSI1116i-eiyy_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7747. WTSIi693-A (HPSI1116i-zies_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7748. WTSIi693-B (HPSI1116i-zies_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7749. WTSIi694-A (HPSI0816i-oemk_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7750. WTSIi697-A (HPSI0516i-dewa_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7751. WTSIi697-B (HPSI0516i-dewa_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7752. WTSIi698-A (HPSI1116i-aimh_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7753. WTSIi698-B (HPSI1116i-aimh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7754. WTSIi699-A (HPSI0916i-hikt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7755. WTSIi699-B (HPSI0916i-hikt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7756. WTSIi700-A (HPSI0115i-iuad_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7757. WTSIi700-B (HPSI0115i-iuad_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7758. WTSIi703-A (HPSI0816i-hizl_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7759. WTSIi703-B (HPSI0816i-hizl_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7760. WTSIi705-A (HPSI0314i-xagu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7761. WTSIi709-A (HPSI0516i-kumr_11)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7762. WTSIi712-A (HPSI1016i-riwg_8)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare genetic neurological disorder

  7763. WTSIi713-A (HPSI0816i-xoga_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7764. WTSIi713-B (HPSI0816i-xoga_12)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7765. WTSIi715-A (HPSI0115i-payf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7766. WTSIi717-A (HPSI0916i-helh_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7767. WTSIi717-B (HPSI0916i-helh_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7768. WTSIi718-A (HPSI0616i-duve_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7769. WTSIi718-B (HPSI0616i-duve_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  7770. WTSIi720-A (HPSI0916i-jejm_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7771. WTSIi722-A (HPSI0115i-jakt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7772. WTSIi726-A (HPSI0115i-boqx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7773. WTSIi727-A (HPSI0115i-bimq_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7774. WTSIi732-A (HPSI0616i-kalo_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_hematologic disease

  7775. WTSIi740-A (HPSI0215i-romx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7776. WYUi001-A

    China Wuyi University (WYU)
    Disease:

    Normal (average)

  7777. WYUi002-A

    China Wuyi University (WYU)
    Disease:

    Normal (average)

  7778. WYUi003-A

    China Wuyi University (WYU)
    Disease:

    Normal (average)

  7779. WYUi004-A (WYU-G6)

    China Wuyi University (WYU)
    Disease:

    Normal (average)

  7780. XACHi004-A

    China Xi'an children's hospital (XACH)
    Disease:

    Atrial fibrillation

  7781. XCHIDi001-A (ZZY250101)

    China Xi'an Children's Hospital (XCHID)
    Disease:

    Primary ciliary dyskinesia

  7782. XDCMHi001-A

    China Xiaoshan District Chinese Medicine Hospital (XDCMH)
    Disease:

    Obsolete_ankylosing spondylitis

  7783. XJHi001-A

    China Xijing Hospital (XJH)
    Disease:

    Fibronectin glomerulopathy

  7784. XMDYYYi001-A (BDU-iPSCs)

    China Department of Neurology, The First Affiliated Hospital of Xiamen University (XMDYYY)
    Disease:

    Becker muscular dystrophy

  7785. XMUi001-A

    China Xiamen University (XMU)
    Disease:

    Primary coenzyme q10 deficiency 7

  7786. XWHNi001-A

    China Department of Neurology, Xuan Wu Hospital (XWHN)
    Disease:

    Alzheimer's disease

  7787. XWHNi002-A

    China Department of Neurology, Xuan Wu Hospital (XWHN)
    Disease:

    Normal (average)

  7788. XWHNi003-A

    China Department of Neurology, Xuan Wu Hospital (XWHN)
    Disease:

    Alzheimer's disease

  7789. XWHNi004-A

    China Department of Neurology, Xuan Wu Hospital (XWHN)
    Disease:

    Normal (average)

  7790. XWHNi005-A

    China Department of Neurology, Xuan Wu Hospital (XWHN)
    Disease:

    Normal (average)

  7791. XXMUFAi001-A

    China The First Affiliated Hospital of Xinxiang Medical University (XXMUFA)
    Disease:

    Long qt syndrome 2

  7792. YBLi001-A (YBL/IPSC01/CONTROL)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7793. YBLi002-A (YBL/IPSC002/CONTROL)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7794. YBLi003-A (YBL/IPSC05/CONTROL)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7795. YBLi004-A (YBL/SH/2018/0062)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7796. YBLi005-A (YBL/OS/2021/00196)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7797. YBLi006-A (YBL/PH/2022/0025)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)

  7798. YBLi007-A (YBL/SH/2018/0067)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7799. YBLi008-A (YBL/SH/2018/0050)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7800. YCMi003-A

    South Korea College of Medicine (YCM)
    Disease:

    Dilated cardiomyopathy

  7801. YCMi004-A

    South Korea College of Medicine (YCM)
    Disease:

    Dilated cardiomyopathy

  7802. YCMi005-A

    South Korea College of Medicine (YCM)
    Disease:

    Dilated cardiomyopathy

  7803. YCMi006-A

    South Korea College of Medicine (YCM)
    Disease:

    Hypertrophic cardiomyopathy

  7804. YCMi007-A

    South Korea College of Medicine (YCM)
    Disease:

    Dilated cardiomyopathy

  7805. YCMi009-A (YCMi009-hDCM009-A)

    South Korea College of Medicine (YCM)
    Disease:

    Obsolete_dilated cardiomyopathy

  7806. YCMi010-A

    South Korea College of Medicine (YCM)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  7807. YSCHi001-A (2AMJH)

    South Korea Severance Children’s Hospital (YSCH)
    Disease:

    Obsolete_epilepsy

  7808. YSCHi002-A (2ABWS)

    South Korea Severance Children’s Hospital (YSCH)
    Disease:

    Obsolete_epilepsy

  7809. YUi002-A (VK0846 #1 and ASmut1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7810. YUi003-A (PB9282 #1 and ASmut2)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7811. YUi004-A (PZ8594 #2 and ASmut3)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7812. YUi005-A (ASmut4 and WD1374 #1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7813. YUi006-A (YO1058 #5 and ASdel1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7814. YUi007-A (SD6010 #3 and ASdel2)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7815. YUi008-A (VE1371 #2 and ASdel3)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7816. YUi009-A (DY5863 #21 and ASupd1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7817. YUi010-A (AK7856 #1 and ASupd2)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7818. YUi011-A (ZM9576 #9 and ASupd3)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7819. YUi012-A (QC7748 #2 and ASupd4)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7820. YUi013-A (UI5640 #8 and ASicd1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7821. YUi014-A (DX6976 #7 and ASicd2)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7822. YUi015-A (SL9656 #4 and ASicd3)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7823. YUi016-A (VJ9612 #5 and ASctr1)

    United States Yale University (YU)
    Disease:

    Normal (average)

  7824. YUi017-A (BT2657 #12 and ASctr2)

    United States Yale University (YU)
    Disease:

    Normal (average)

  7825. YUi018-A (SF6987 #1 and ASctr3)

    United States Yale University (YU)
    Disease:

    Normal (average)

  7826. YUi019-A (BW3595 #3 and ASctr4)

    United States Yale University (YU)
    Disease:

    Normal (average)

  7827. YUCMi020-A

    South Korea Yonsei University College of Medicine (YUCM)
    Disease:

    Normal (average)

  7828. YUCMi022-A (hiPSC-KCNH2_G53S)

    South Korea Yonsei University College of Medicine (YUCM)
    Disease:

    Long qt syndrome

  7829. YUCMi024-A (hiPSC-KCNQ1_G245G_2)

    South Korea Yonsei University College of Medicine (YUCM)
    Disease:

    Long qt syndrome

  7830. YUCMi025-A (hiPSC-KCNQ1_G245G_1)

    South Korea Yonsei University College of Medicine (YUCM)
    Disease:

    Long qt syndrome

  7831. ZEENTi001-A (OTOF/A-iPSC)

    China Department of Otorhinolaryngology, Second Affiliated Hospital, Zhejiang University School of Medicine (ZEENT)
    Disease:

    Autosomal recessive nonsyndromic deafness 9

  7832. ZEENTi002-A

    China Department of Otorhinolaryngology, Second Affiliated Hospital, Zhejiang University School of Medicine (ZEENT)
    Disease:

    Autosomal recessive nonsyndromic deafness 9

  7833. ZIPi013-B (ZIP13 clone 2)

    Germany Zentrum für Integrative Psychiatrie-ZiP gGmbH, Stem Cell Lab (ZIP)
    Disease:

    Normal (average)

  7834. ZJSHi001-A (ZJSHi-KCNB1)

    China Department of Pediatrics, The Second Affiliated Hospital of Zhejiang University School of Medicine (ZJSH)
    Disease:

    Developmental and epileptic encephalopathy, 26

  7835. ZJUi009-A (ZJULLi001-A)

    China Zhejiang University (ZJU)
    Disease:

    Marfan syndrome

  7836. ZJUi010-A (ZJULLi002-A and 161103SPYLQTFSDC12)

    China Zhejiang University (ZJU)
    Disease:

    Long qt syndrome

  7837. ZJUi011-A (ZJULLi003-A and LSYMYH7iPS)

    China Zhejiang University (ZJU)
    Disease:

    Hypertrophic cardiomyopathy

  7838. ZJUi012-A (ZJULLi004-A and ZYLMYBPC3iPS)

    China Zhejiang University (ZJU)
    Disease:

    Hypertrophic cardiomyopathy

  7839. ZJUCi001-A

    China Zhejiang children hospital (ZJUC)
    Disease:

    Dilated cardiomyopathy

  7840. ZJUCHi003-A

    China The Children's Hospital, Zhejiang University School of Medicine (ZJUCH)
    Disease:

    Temple-baraitser syndrome

  7841. ZJULLi002-A (ZJULLi005-A and JMLMYH6iPSC)

    China Zhejiang University Lianglab (ZJULL)
    Disease:

    Hypertrophic cardiomyopathy 14

  7842. ZJULLi006-A

    China Zhejiang University Lianglab (ZJULL)
    Disease:

    Brugada syndrome

  7843. ZJULLi007-A

    China Zhejiang University Lianglab (ZJULL)
    Disease:

    Normal (average)

  7844. ZJULLi009-A (YYY-iPSC)

    China Zhejiang University Lianglab (ZJULL)
    Disease:

    Wilson disease

  7845. ZJULLi010-A (ZWM-iPSC)

    China Zhejiang University Lianglab (ZJULL)
    Disease:

    Fabry disease

  7846. ZOCi001-A

    China Zhongshan Ophthalmic Center (ZOC)
    Disease:

    Retinitis pigmentosa

  7847. ZSPHARi002-A

    China Department of Pharmacy (ZSPHAR)
    Disease:

    Kidney disorder

  7848. ZSZOCi001-A

    China Zhongshan Ophthalmic Center (ZSZOC)
    Disease:

    Knobloch syndrome

  7849. ZZUi004-A (ZZU-iPS-SCA3-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 3

  7850. ZZUi005-A (ZZU-iPS-PD-RAB39b-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_parkinson's disease

  7851. ZZUi006-A (ZZU-iPS-DM1-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Steinert myotonic dystrophy

  7852. ZZUi007-A (ZZU-iPS-PD-CHCHD2-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_parkinson's disease

  7853. ZZUi009-A (ZZU-iPS-AD-PS1-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_alzheimer's disease

  7854. ZZUi010-A (ZZU-iPS-AD-APP-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_alzheimer's disease

  7855. ZZUi011-A (ZZU-iPS-Normal-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7856. ZZUi012-A (ZZU-iPS-PFBC-SLC20A2-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Bilateral striopallidodentate calcinosis

  7857. ZZUi013-A (ZZU-iPS-AD-MEOX2-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_alzheimer's disease

  7858. ZZUi014-A (ZZU-iPS-SCA3-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 3

  7859. ZZUi015-A (ZZU-iPS-DM1-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Myotonic dystrophy type 1

  7860. ZZUi016-A

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7861. ZZUi017-A (ZZU-iPS-SCA6-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 6

  7862. ZZUi018-A (ZZU-iPS-SCA6-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7863. ZZUi019-A (ZZU-iPS-Normal-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7864. ZZUi024-A (ZZU-iPS-AD-APP-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Alzheimer's disease

  7865. ZZUi026-A (ZZU-iPS-SCA3-003)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 3

  7866. ZZUi027-A (ZZU-iPS-PD-RAB39b-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Parkinson disease

  7867. ZZUi028-A (ZZU-iPS-Normal-005)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7868. ZZUi030-A (ZZU-iPS-SPG7-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Spastic paraplegia type 7

  7869. ZZUi031-A (ZZU-iPS-Normal-006)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7870. ZZUi036-A (ZZU-iPS-NIID-NOTCH2NLC-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7871. ZZUi037-A (ZZU-iPS-SCA3-004)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 3

  7872. ZZUCSBi001-A

    China Shu-Ang Li (ZZUCSB)
    Disease:

    Normal (average)

  7873. ZZUNEUi001-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Normal (average)

  7874. ZZUNEUi002-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Spinocerebellar ataxia type 3

  7875. ZZUNEUi003-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Wilson disease

  7876. ZZUNEUi004-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Wilson disease

  7877. ZZUNEUi005-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Wilson disease

  7878. ZZUNEUi010-A (CMF001-A)

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Juvenile amyotrophic lateral sclerosis

  7879. ZZUNEUi026-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Hypertrophic cardiomyopathy

  7880. ZZUNEUi027-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Long qt syndrome 2

  7881. ZZUNEUi028-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Hypertrophic cardiomyopathy

  7882. ZZUNEUi029-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Hypercholesterolemia

  7883. ZZUNEUi030-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Long qt syndrome

  7884. ZZUSAHi004-A

    China The Second Affiliated Hospital of Zhengzhou University (ZZUSAH)
    Disease:

    Familial long qt syndrome