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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Cardiomyopathy

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

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

    Cardiomyopathy

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

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

    Cardiomyopathy

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Cardiomyopathy

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

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

    Cardiomyopathy

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Cardiomyopathy

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

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

    Cardiomyopathy

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

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

    Cardiomyopathy

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

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

    Cardiomyopathy

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Cardiomyopathy

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

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

    Cardiomyopathy

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

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

    Cardiomyopathy

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

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

    Cardiomyopathy

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Cardiomyopathy

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

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

    Normal (average)

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

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

    Cardiomyopathy

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

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

    Skeletal myopathy

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

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

    Normal (average)

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

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

    Skeletal myopathy

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Skeletal myopathy

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

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

    Laminopathy

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

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

    Normal (average)

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

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

    Laminopathy

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

  121. AMUFAHi001-A

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

    Normal (average)

  122. AMUFAHi002-A (AY20210813)

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

    Polycystic ovary syndrome

  123. AMUFAHi003-A

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

    Normal (average)

  124. RUCDRi002-A-72

    Austria Angios GmbH (ANGIOS)
    Disease:

    Normal (average)

  125. AOUMEYi002-A

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

    Gm3 synthase deficiency

  126. AOUMEYi003-A

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

    Morquio syndrome

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Normal (average)

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

  130. ASGRCi004-A (0118 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Proliferative diabetic retinopathy

    Disease:

    Type 2 diabetes mellitus

  131. ASGRCi005-A (0622 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Keratoconjunctivitis sicca

  132. ASGRCi006-A (0808 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Proliferative diabetic retinopathy

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

  134. ATCi002-A

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

    Keipert syndrome

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

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

    Hepatocyte nuclear factor 1-alpha-associated monogenic diabetes

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

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

    Hepatocyte nuclear factor 1-alpha-associated monogenic diabetes

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Maturity-onset diabetes of the young type 10

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

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

    Maturity-onset diabetes of the young type 10

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Maturity-onset diabetes of the young type 10

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

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

    Diabetes mellitus

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

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

    Diabetes mellitus

  151. AUi001-A

    Denmark Aarhus University (AU)
    Disease:

    Herpes simplex encephalitis

  152. AUMCi001-A (LUMC0195iFOXC)

    Netherlands Amsterdam University Medical Centers (AUMC)

  153. AUMCi001-A-1

    Netherlands Amsterdam University Medical Centers (AUMC)

  154. AUMCi002-A (LUMC0203iOCA)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Oculocutaneous albinism type 1a

  155. AUMCi003-A (LUMC0147iXLRS)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    X-linked retinoschisis

  156. AUMCi004-A (LUMC0181iXLRS)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    X-linked retinoschisis

  157. AUMCi005-A (LUMC0182iXLRS)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    X-linked retinoschisis

  158. AUMCi006-A (LUMC0196iOAT)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Gyrate atrophy of choroid and retina

  159. AUMCi007-A (LUMC0204iOAT)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Gyrate atrophy of choroid and retina

  160. AUMCi008-A (LUMC0296iOAT)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Gyrate atrophy of choroid and retina

  161. AUMCi009-A (LUMC0251iSLC)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

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

  162. AUMCi010-A (LF2A_C02 and LUMC0255iHCM02)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  163. AUMCi010-B (LUMC0255iHCM03 and LF2A_C03)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  164. AUMCi010-C (LF2A_C04 and LUMC0255iHCM04)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  165. AUMCi010-D (LF2A_C01 and LUMC0255iHCM01)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  166. AUMCi010-E (LF2A_C05 and LUMC0255iHCM05)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  167. AUMCi010-F (LUMC0255iHCM06 and LF2A_C06)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  168. AUMCi011-A (LF2B_C01 and LUMC0258iHCM01)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  169. AUMCi011-B (LUMC0258iHCM04 and LF2B_C04)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  170. AUMCi011-C (LUMC0258iHCM05 and LF2B_C05)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  171. AUMCi011-D (LUMC0258iHCM02 and LF2B_C02)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  172. AUMCi011-E (LUMC0258iHCM03 and LF2B_C03)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  173. AUMCi011-F (LUMC0258iHCM06 and LF2B_C06)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  174. AUMCi012-A (LUMC0281iHCM10 and LF3A_C10)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  175. AUMCi012-B (LF3A_C14 and LUMC0281iHCM14)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  176. AUMCi012-C (LF3A_C15 and LUMC0281iHCM15)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  177. AUMCi012-D (LF3A_C01 and LUMC0281iHCM01)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  178. AUMCi012-E (LF3A_C03 and LUMC0281iHCM03)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  179. AUMCi012-F (LUMC0281iHCM06 and LF3A_C06)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  180. AUMCi013-A (LUMC0282iHCM02 and LF3B_C02)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  181. AUMCi013-B (LF3B_C04 and LUMC0282iHCM04)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  182. AUMCi013-C (LF3B_C05 and LUMC0282iHCM05)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  183. AUMCi013-D (LF3B_C03 and LUMC0282iHCM03)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  184. AUMCi013-E (LF3B_C09 and LUMC0282iHCM09)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  185. AUMCi013-F (LF3B_C14 and LUMC0282iHCM14)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  186. AUMCi014-A (LF3C_C02 and LUMC0283iHCM02)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  187. AUMCi014-B (LF3C_C05 and LUMC0283iHCM05)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  188. AUMCi014-C (LF3C_C07 and LUMC0283iHCM07)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  189. AUMCi014-D (LF3C_C01 and LUMC0283iHCM01)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  190. AUMCi014-E (LF3C_C03 and LUMC0283iHCM03)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  191. AUMCi014-F (LUMC0283iHCM06 and LF3C_C06)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  192. AUMCi014-G (LF3C_C09 and LUMC0283iHCM09)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  193. AUMCi014-H (MF3C_C08)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  194. AUMCi014-I (MF3C_C20)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  195. AUMCi014-J (MF3C_C31)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  196. AUMCi015-A

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Dilated cardiomyopathy

  197. AUSCIi001-A

    Turkey Ankara University Stem Cell Institute (AUSCI)
    Disease:

    Spinal muscular atrophy

  198. BAFYi001-A

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

    Edwards syndrome

  199. BBANTWi001-A (iPSC_FB_M45-50_C9)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  200. BBANTWi001-B (iPSC_FB_M45-50_C15)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  201. BBANTWi001-C (iPSC_FB_M45-50_C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  202. BBANTWi006-A (iPSC_BrS9_FB_C7)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome 1

  203. BBANTWi007-A (iPSC_BrS10_FB_C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome 1

  204. BBANTWi008-A (iPSC_PBMC_LDS_SMAD3_T1_C11)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 3

  205. BBANTWi009-A

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Meester-loeys syndrome

  206. BBANTWi010-A (iPSC_PBMC_LDS_TGFB3_KE2M_C9)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 5

  207. BBANTWi011-A

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Familial thoracic aortic aneurysm and aortic dissection

  208. BBANTWi012-A (F1990.01 C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  209. BBANTWi012-A-1 (TTN_E48_V4623*)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

  210. BBANTWi012-A-2 (iPSC_FB_F19901C3_TTN_E48_L4612*)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

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

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

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

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

  213. BBANTWi012-A-5 (iPSC_F199001_C3_CRISPR_CACNA1C_T330M_HMZ_C6)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome

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

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome

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

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

    Normal (average)

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

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

    Alzheimer's disease

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  305. BCHi026-A-3 (HNDS0136-01#A CNC9(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  396. BCHi049-A (1383.1)

    United States Children's Hospital (BCH)
    Disease:

    Normal (average)

  397. BCHNi001-A (BCHi001-A)

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

    Bardet-biedl syndrome

  398. BCHNCi001-A

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

    Early infantile developmental and epileptic encephalopathy

  399. BCHNCi003-A

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

    Mitochondrial pyruvate carrier deficiency

  400. BCHNDi001-A

    China 徐超龙 (BCHND)
    Disease:

    Mitochondrial encephalomyopathy

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

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal (average)

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

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal (average)

  403. BCMi002-A (LZ02)

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal (average)

  404. BCMi003-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked mental retardation syndrome

  405. BCMi004-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked mental retardation syndrome

  406. BCMi005-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked mental retardation syndrome

  407. BCMi006-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked mental retardation syndrome

  408. BCMi007-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked mental retardation syndrome

  409. BCRTi001-A (P01-1)

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

    Fibrodysplasia ossificans progressiva

  410. BCRTi002-A (P02-1)

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

    Fibrodysplasia ossificans progressiva

  411. BCRTi004-A

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

    Normal (average)

  412. BCRTi005-A

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

    Normal (average)

  413. BCRTi006-A

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

    Focal segmental glomerulosclerosis

  414. BCRTi007-A

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

    Polycystic kidney disease

  415. BCRTi009-A

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

    Diabetic nephropathy

  416. BCRTi010-A

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

    Normal (average)

  417. BCRTi011-A

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

    Neurofibromatosis type 1

  418. BFVSBi001-A

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

    Arterial calcification

  419. BFVSBi003-A

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

    Ehlers-danlos syndrome, vascular type

  420. BFVSBi004-A

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

    Ehlers-danlos syndrome, vascular type

  421. BFVSBi005-A

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

    Covid-19

  422. BFVSBi006-A

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

    Varicose veins

  423. BFVSBi007-A

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

    Melanoma

  424. BFVSBi008-A

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

    Loeys-dietz syndrome

  425. BGUi001-A (BGU01iPORhet)

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

    P450 oxidoreductase deficiency

  426. BGUi002-A (BGU02iPOR)

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

    P450 oxidoreductase deficiency

  427. BGUi003-A (BGU03iPOR)

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

    P450 oxidoreductase deficiency

  428. BGUi004-A (BGU101iCCHS)

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

    Congenital central hypoventilation syndrome

  429. BGUi005-A (BGU102iCCHS)

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

    Congenital central hypoventilation syndrome

  430. BGUi008-A (DCM-C)

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

    Left ventricular noncompaction cardiomyopathy

  431. BGUi009-A (DCM-O)

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

    Left ventricular noncompaction cardiomyopathy

  432. BGUi010-A (DCM-R)

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

    Left ventricular noncompaction cardiomyopathy

  433. BGUi011-A (BGU01iGRIN2D)

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

    Developmental and epileptic encephalopathy, 46

  434. BGUi012-A (BGU02iGRIN2D CTR)

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

  437. BGUi015-A (BGUiBJ)

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

    Normal (average)

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Alzheimer disease

  443. BIHi001-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  444. BIHi001-B-1

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  445. BIHi001-B-7

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  446. BIHi001-B-8

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  447. BIHi001-B-9

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  448. BIHi001-B-10

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  449. BIHi001-B-13

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  450. BIHi002-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Autosomal recessive osteopetrosis 4

  451. BIHi004-A (NHDF Epi5 Cl5 iPSC)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  452. BIHi004-B (NHDF Epi5 Cl2 iPSC)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  453. BIHi005-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  454. BIHi005-A-4

    Germany Berlin Institute of Health (BIH)
    Disease:

    Myocardial infarction

  455. BIHi005-A-5

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_alzheimer's disease

  456. BIHi005-A-64

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  457. BIHi005-A-86

    Germany Berlin Institute of Health (BIH)
    Disease:

    Kit np_000213.1:p.d816v

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Kit np_000213.1:p.d816v

  459. BIHi005-A-92

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  460. BIHi005-A-93

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  461. BIHi005-A-94

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obesity

  462. BIHi005-A-95

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  463. BIHi005-A-97

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obesity

  464. BIHi005-A-F

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obesity

  465. BIHi006-D

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  466. BIHi007-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  467. BIHi008-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  468. BIHi009-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  469. BIHi010-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  470. BIHi011-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  471. BIHi012-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  474. BIHi015-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  475. BIHi016-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  476. BIHi017-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  477. BIHi018-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  478. BIHi019-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  479. BIHi024-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  480. BIHi025-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  481. BIHi028-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  482. BIHi029-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  483. BIHi030-C

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  484. BIHi031-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  485. BIHi032-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  486. BIHi038-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  487. BIHi044-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Allan-herndon-dudley syndrome

  488. BIHi045-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Allan-herndon-dudley syndrome

  489. BIHi045-A-2

    Germany Berlin Institute of Health (BIH)
    Disease:

    Allan-herndon-dudley syndrome

  490. BIHi049-A (SCVI-112)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Donnai-barrow syndrome

  492. BIHi250-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  493. BIHi261-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obesity due to pro-opiomelanocortin deficiency

  494. BIHi261-A-1

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obesity due to pro-opiomelanocortin deficiency

  495. BIHi263-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-related cognitive impairment

  496. BIHi264-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  497. BIHi265-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  498. BIHi266-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  499. BIHi267-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

  500. BIHi269-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  501. BIHi271-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  502. BIHi272-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-related cognitive impairment

  503. BIHi273-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  504. BIHi276-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

  505. BIHi289-C

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  506. BIHi289-E

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  507. BIHi290-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  509. BIHi291-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  510. BIHi292-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Nasu-hakola disease

  511. BIHi294-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  512. BIHi296-A (03-17B)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  513. BIHi296-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  514. BIHi300-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-related cognitive impairment

  515. BIOi002-A

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Autosomal dominant optic atrophy

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

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Hereditary retinal dystrophy

  517. BIOi004-A

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Retinitis pigmentosa 33

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Frontotemporal dementia

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Huntington disease

  525. STBCi006-A-1 (ApoE KO)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  528. BIONi010-A (K1P53)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Inflammatory disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  558. 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)

  559. 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)

  560. 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)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

  565. BIONi010-C-72

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  573. BIONi016-A (H310715 47-1)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  583. BIONi026-A (H300715 48-3)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  590. BIONi033-A (H180615 and SAMEA4563389)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  591. BIONi034-A (H290715 and SAMEA4563391)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  592. BIONi035-A (H180815 and SAMEA4563393)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  595. BIORTCi001-A (BAiPSC 000 and OSTiFGM2)

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

    Normal (average)

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

    Hungary BioTalentum Ltd. (BIOT)
    Disease:

    Obsolete_alzheimer's disease

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

    Hungary BioTalentum Ltd. (BIOT)
    Disease:

    Alzheimer disease

  598. BIUi001-A (T1A1i-001)

    Israel Bar Ilan University (BIU)
    Disease:

    Obsolete: nuclear cell envelopathy

  599. BIUi002-A (T1A1i-002)

    Israel Bar Ilan University (BIU)
    Disease:

    Obsolete: nuclear cell envelopathy

  600. BJTTHi001-A

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Normal (average)

  601. BJTTHi001-A-1

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  602. BJTTHi001-A-2

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Dravet syndrome

    Disease:

    Epilepsy

  603. BJTTHi001-A-3

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  604. BJTTHi001-A-4

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  605. BJTTHi001-A-5

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  606. BJTTHi003-A (CARASIL WHN1C2)

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Carasil syndrome

  607. BRCi014-A (1383D6 and HPS1006)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Normal (average)

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

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Oligodendrocyte

  609. BRCi021-A (TUH1)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Cardiomyopathy

  610. BRCi024-A (HiPS-RTT_CUH01)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  611. BRCi025-A (HiPS-RTT_CUH02)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  612. BRCi026-A (HiPS-RTT_CUH05)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  613. BRCi027-A (HiPS-RTT_CUH06)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  614. BRCi036-A (HiPS-GLUT1DS1)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Classic glucose transporter type 1 deficiency syndrome

  615. BRCi037-A (HiPS-GLUT1DS2)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Classic glucose transporter type 1 deficiency syndrome

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

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

    Retinitis pigmentosa

  620. BTHBIOi002-A

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

    Usher syndrome

  621. BTHBIOi003-A

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

    Leber congenital amaurosis

  622. BTHBIOi004-A

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

    Oculocutaneous albinism type 2

  623. BTHBIOi005-A

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

    Retinitis pigmentosa

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

    China Beijing Institute of Ophthalmology for BeijingTongren Hospital (BTHBIO)

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

    United States Boston University (BUCREM)
    Disease:

    Lethal brain and heart developmental defects

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

    United States Boston University (BUCREM)
    Disease:

    Lethal brain and heart developmental defects

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

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

    Retinitis pigmentosa

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

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

    Age-related macular degeneration

  629. CAMi001-A (KiPS c1)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  630. CAMi002-A (FiPS 2a)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  631. CAMi002-B (FiPS 2b)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  632. CAMi002-C (FiPS 2c)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  633. CAMi004-A (AdiPS 1)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  634. CAMi005-A (O27Tat)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  635. CAMi005-B (2F8)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  636. CAMi014-A (A1ATD1)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Alpha-1-antitrypsin deficiency

  637. CBi001-A (XLC-348)

    United States Creative Bioarray (CB)
    Disease:

    Obsolete_schizophrenia

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

    United States Creative Bioarray (CB)
    Disease:

    Obsolete_schizophrenia

  639. CBCHi001-A-1

    China Beijing Chest Hospital (CBCH)
    Disease:

    Hypertrophic cardiomyopathy

  640. CBDTi001-A

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

    Normal (average)

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

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

    Normal (average)

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

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

    Parkinson disease

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

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

    Parkinson disease

  644. 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

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Intellectual disability

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

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

    Amyotrophic lateral sclerosis

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Amyotrophic lateral sclerosis

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

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

    Intellectual disability

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

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

    Parkinson disease

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

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

    Amyotrophic lateral sclerosis

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

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

    Amyotrophic lateral sclerosis

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Intellectual disability

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

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

    Parkinson disease

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

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

    Machado-joseph disease

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

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

    Parkinson disease

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

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

    Amyotrophic lateral sclerosis

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

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

    Intellectual disability

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Intellectual disability

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

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

    Amyotrophic lateral sclerosis

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

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

    Amyotrophic lateral sclerosis

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

  687. CBIGi001-B (IPSC0064)

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

    Normal (average)

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

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

    Normal (average)

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

  693. CBIGi004-A (IPSC0034)

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

    Normal (average)

  694. CBIGi005-A (IPSC0003 and LRRK2 G2019S)

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

  700. CBIGi008-A (IPSC0011 and GBA T369M)

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

  704. CBIGi010-A (SOD1 A4S and IPSC0014)

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

    Amyotrophic lateral sclerosis

  705. CBIGi011-A (SOD1 I114T and IPSC0015)

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

    Amyotrophic lateral sclerosis

  706. CBIGi012-A (IPSC0016)

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

    Normal (average)

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

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

    Parkinson disease

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

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

    Parkinson disease

  709. CBIGi014-A (VAPB A2V and IPSC0019)

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

    Amyotrophic lateral sclerosis

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

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

    Parkinson disease

  711. 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

  712. CBIGi017-A (IPSC0022)

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

    Normal (average)

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

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

    Normal (average)

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

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

    Intellectual disability

  715. CBIGi018-B (TD02 and IPSC0035)

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

    Normal (average)

  716. CBIGi019-A (IPSC0025)

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

    Normal (average)

  717. CBIGi020-A (IPSC0026)

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

    Amyotrophic lateral sclerosis

  718. CBIGi021-A (GBA1 L324I and IPSC0027)

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

    Parkinson disease

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

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

    Amyotrophic lateral sclerosis

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

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

    Amyotrophic lateral sclerosis

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

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

    Amyotrophic lateral sclerosis

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

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

    Amyotrophic lateral sclerosis

  723. CBIGi025-A (IPSC0032)

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

    Amyotrophic lateral sclerosis

  724. CBIGi026-A (IPSC0036)

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

    Normal (average)

  725. CBIGi026-B (IPSC0095)

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

    Normal (average)

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

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

    Parkinson disease

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

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

    Parkinson disease

  728. CBIGi028-A (IPSC0038)

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

    Normal (average)

  729. CBIGi029-A (IPSC0040)

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

    Parkinson disease

  730. CBIGi030-A (IPSC0041)

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

    Parkinson disease

  731. CBIGi031-A (IPSC0042)

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

    Parkinson disease

  732. CBIGi032-A (IPSC0043)

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

  736. CBIGi033-A (IPSC0044)

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

    Normal (average)

  737. CBIGi034-A (IPSC0045)

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

    Normal (average)

  738. CBIGi035-A (IPSC0046)

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

    Normal (average)

  739. CBIGi036-A (IPSC0047)

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

    Parkinson disease

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

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

    Parkinson disease

  741. CBIGi038-A (IPSC0049)

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

    Amyotrophic lateral sclerosis

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

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

    Parkinson disease

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

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

    Parkinson disease

  744. 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

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

  749. CBIGi043-A (IPSC0057)

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

    Amyotrophic lateral sclerosis

  750. 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

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

  754. CBIGi046-A (IPSC0087)

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

    Normal (average)

  755. CBIGi046-B (IPSC0088)

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

    Normal (average)

  756. CBIGi047-A (IPSC0091)

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

    Amyotrophic lateral sclerosis

  757. CBIGi048-A (IPSC0092)

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

    Amyotrophic lateral sclerosis

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

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

    Amyotrophic lateral sclerosis

  759. CBIGi050-A (IPSC0094)

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

    Parkinson disease

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

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

    Normal (average)

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

  764. CBRCULi005-A (91-3158-1)

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

    Myotonic dystrophy type 1

  765. CBRCULi006-A (59-0116-24)

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

    Normal (average)

  766. CBRCULi007-A (14-0730-1)

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

    Myotonic dystrophy type 1

  767. CBRCULi008-A (522-0617-1)

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

    Normal (average)

  768. CBRCULi009-A (522-1839-4)

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

    Normal (average)

  769. CBRCULi010-A (GM00498E-1 and GM00498E clone 1)

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

    Normal (average)

  770. CBRCULi011-A (GM00969F-2 and GM00969F clone 2)

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

    Normal (average)

  771. CBRCULi012-A (GM04601 clone 21 and GM04601-21)

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

    Myotonic dystrophy type 1

  772. CBRCULi013-A (GM04602-2 and GM04602 clone 2)

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

    Myotonic dystrophy type 1

  773. CBRCULi014-A (AG09393A clone 3 and AG09393A-3)

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

    Normal (average)

  774. CBRCULi015-A (GM23375-1 and GM23375 clone 1)

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

    Congenital myotonic dystrophy

  775. CBRCULi016-A (SCN5A p.R219H-14C)

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

    Dilated cardiomyopathy

  776. CBRCULi016-A-1 (SCN5A p.R219H-14C-ISO)

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

    Dilated cardiomyopathy

  777. CBRCULi017-A (SCN5A p.R219-22B)

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

    Normal (average)

  778. CBRCULi018-A (91-2032-7)

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

    Myotonic dystrophy type 1

  779. CBRCULi019-A (19-1741-2)

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

    Myotonic dystrophy type 1

  780. CBRCULi020-A (79-1761-15)

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

    Myotonic dystrophy type 1

  781. CCMi001-A (DMD1)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Duchenne muscular dystrophy

  782. CCMi007-A (SAS1 C5)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  783. CCMi008-A (SAS2 C1)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  784. CCMi009-A (SAS3 C10)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  785. CCMi011-A (SAS7 C6)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  786. CCMi012-A (LMNA_SP_C3)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Dilated cardiomyopathy

  787. TMOi001-A-1 (hiPSC-CD34-GFP-3G6)

    Austria St. Anna Kinderkrebsforschung GmbH (CCRI)
    Disease:

    Normal (average)

  788. CDIi001-A (01279)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  789. CDIi002-A (01434)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  790. CDIi004-A (11713)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  791. CDIi011-A (21527)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  792. CDIi013-A (PPMI_3409 and FCDI_11287)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  793. CDIi014-A (FCDI_11292 and PPMI_4055)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  794. CDIi015-A (PPMI_3419 and FCDI_11294)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  795. CDIi016-A (PPMI_3411 and FCDI_11295)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  796. CDIi017-A (PPMI_3446 and FCDI_11296)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  797. CDIi018-A (PPMI_3234 and FCDI_11298)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  798. CDIi019-A (PPMI_52062 and FCDI_11299)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  799. CDIi019-A-1

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  800. CDIi019-A-2

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  801. CDIi020-A (PPMI_54144 and FCDI_11300)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  802. CDIi021-A (PPMI_3459 and FCDI_11301)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  803. CDIi022-A (FCDI_11302 and PPMI_3460)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  804. CDIi023-A (FCDI_11303 and PPMI_3448)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  805. CDIi024-A (FCDI_11305 and PPMI_51867)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  806. CDIi025-A (FCDI_11306 and PPMI_40273)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  807. CDIi026-A (FCDI_11307 and PPMI_51625)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  808. CDIi027-A (FCDI_11308 and PPMI_3186)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  809. CDIi028-A (PPMI_3664 and FCDI_11309)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  810. CDIi029-A (PPMI_3665 and FCDI_11310)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  811. CDIi030-A (FCDI_11311 and PPMI_3668)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  812. CDIi031-A (PPMI_3451 and FCDI_11312)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  813. CDIi032-A (FCDI_11313 and PPMI_3658)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  814. CDIi033-A (FCDI_11314 and PPMI_3465)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  815. CDIi034-A (PPMI_51440 and FCDI_11317)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  816. CDIi035-A (PPMI_51330 and FCDI_11318)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  817. CDIi036-A (PPMI_42072 and FCDI_11319)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  818. CDIi037-A (PPMI_52530 and FCDI_11321)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  819. CDIi038-A (FCDI_11323 and PPMI_53339)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  820. CDIi039-A (FCDI_11325 and PPMI_56761)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  821. CDIi040-A (FCDI_11327 and PPMI_3220)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  822. CDIi041-A (FCDI_11328 and PPMI_56435)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  823. CDIi042-A (PPMI_41486 and FCDI_11329)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  824. CDIi043-A (PPMI_54262 and FCDI_11331)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  825. CDIi044-A (PPMI_50184 and FCDI_11334)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  826. CDIi045-A (FCDI_11337 and PPMI_3952)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  827. CDIi046-A (FCDI_11340 and PPMI_56779)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  828. CDIi047-A (FCDI_11341 and PPMI_3471)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  829. CDIi048-A (PPMI_3453 and FCDI_11342)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  830. CDIi049-A (PPMI_3480 and FCDI_11343)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  831. CDIi050-A (PPMI_4098 and FCDI_11344)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  832. CDIi050-A-1

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  833. CDIi050-A-2

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  834. CDIi051-A (PPMI_3452 and FCDI_11345)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  835. CDIi052-A (PPMI_4091 and FCDI_11346)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  836. CDIi053-A (PPMI_3422 and FCDI_11347)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  837. CDIi054-A (FCDI_11348 and PPMI_50086)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  838. CDIi055-A (FCDI_11349 and PPMI_60003)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  839. CDIi056-A (PPMI_51971 and FCDI_11353)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  840. CDIi057-A (PPMI_56954 and FCDI_11355)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  841. CDIi058-A (FCDI_11362 and PPMI_51755)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  842. CDIi059-A (PPMI_52828 and FCDI_11363)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  843. CDIi060-A (FCDI_11370 and PPMI_55251)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  844. CDIi061-A (FCDI_11371 and PPMI_55380)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  845. CDIi062-A (FCDI_11436 and PPMI_90456)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  846. CDIi063-A (FCDI_11437 and PPMI_3473)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  847. CDIi064-A (PPMI_3475 and FCDI_11438)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  848. CDIi065-A (PPMI_3588 and FCDI_11442)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  849. CDIi066-A (FCDI_11446 and PPMI_4111)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  850. CDIi067-A (FCDI_11447 and PPMI_3960)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  851. CDIi068-A (FCDI_11448 and PPMI_51518)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  852. CDIi069-A (PPMI_3666 and FCDI_11449)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  853. CDIi070-A (FCDI_11450 and PPMI_3966)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Normal (average)

  854. CDIi071-A (PPMI_4108 and FCDI_11455)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  855. CDIi072-A (FCDI_11459 and PPMI_4101)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  856. CDIi073-A (PPMI_52400 and FCDI_11460)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  857. CDIi074-A (PPMI_54908 and FCDI_11462)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  858. CDIi075-A (PPMI_54991 and FCDI_11463)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  859. CDIi076-A (PPMI_56680 and FCDI_11465)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  860. CDIi077-A (PPMI_3469 and FCDI_11468)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  861. CDIi078-A (FCDI_11469 and PPMI_3467)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  862. CDIi079-A (PPMI_57670 and FCDI_11471)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  863. CDIi080-A (FCDI_11473 and PPMI_51844)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  864. CDIi081-A (PPMI_57447 and FCDI_11474)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  865. CDIi082-A (PPMI_4099 and FCDI_11475)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  866. CDIi083-A (PPMI_52524 and FCDI_11478)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  867. CDIi084-A (FCDI_11483 and PPMI_57292)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  868. CDIi085-A (FCDI_11484 and PPMI_3954)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  869. CDIi086-A (PPMI_18567 and FCDI_11486)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  870. CDIi087-A (PPMI_4106 and FCDI_11491)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  871. CDIi088-A (PPMI_4107 and FCDI_11492)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  872. CDIi089-A (FCDI_11493 and PPMI_4109)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  873. CDIi090-A (FCDI_11494 and PPMI_4110)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  874. CDIi091-A (FCDI_11498 and PPMI_51714)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  875. CDIi092-A (FCDI_11500 and PPMI_56169)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  876. CDIi093-A (PPMI_3953 and FCDI_11505)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  877. CDIi094-A (FCDI_11508 and PPMI_52517)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  878. CDIi095-A (FCDI_11512 and PPMI_53988)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  879. CDIi096-A (FCDI_11526 and PPMI_57961)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  880. CDIi097-A (FCDI_11527 and PPMI_3591)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  881. CDIi098-A (FCDI_11545 and PPMI_52932)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  882. CDIi099-A (FCDI_11546 and PPMI_53518)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  883. CDIi100-A (FCDI_11555 and PPMI_42378)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  884. CDIi101-A (FCDI_11556 and PPMI_40760)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  885. CDIi102-A (FCDI_11557 and PPMI_41430)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  886. CDIi103-A (FCDI_11571 and PPMI_58182)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  887. CDIi104-A (FCDI_11578 and PPMI_54048)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Prodromal period

    Disease:

    Parkinson disease

  888. CDIi105-A (PPMI_41568 and FCDI_14555)

    United States FUJIFILM Cellular Dynamics, Inc. (CDI)
    Disease:

    Parkinson disease

  889. CEBi001-A (Cellartis Human iPS Cell Line 22)

    France Takara Bio Europe AB (former Cellartis) (CEB)
    Disease:

    Normal (average)

  890. CEGHUi001-A (iPSC_CEGH_C2)

    Brazil Human Genome and Stem Cell Research Center, University of São Paulo (CEGHU)
    Disease:

    Normal (average)

  891. CENSOi001-B (FB78R2c2 and CENSOi249)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  892. CENSOi002-B (FB74R2c4 and CENSOi261)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  893. CENSOi003-B (FB79R2c6 and CENSOi258)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  894. CENSOi005-A (FB76R2c5 and CENSOi245)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  895. CENSOi007-A (FB75R2c5 and CENSOi255)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  896. CENSOi008-A (FB77R2c3 and CENSOi260)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Myotonic dystrophy type 1

  897. CHCMUi001-A

    China Children's hospital of Chongqing Medical University (CHCMU)
    Disease:

    Activated pi3k-delta syndrome

  898. CHCMUi002-A

    China Children's hospital of Chongqing Medical University (CHCMU)
    Disease:

    Chronic granulomatous disease

  899. CHDIi001-A (#1c8 and CHDI-90002149)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  900. CHDIi002-A (#2c3 and CHDI-90002150)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  901. CHDIi003-A (#3c1 and CHDI-90002151)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  902. CHDIi004-A (#4c2 and CHDI-90002152)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  903. CHDIi005-A (#5c4 and CHDI-90002153)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  904. CHDIi006-A (#6c7 and CHDI-90002154)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  905. CHDIi008-A (#8c3 and CHDI-90002156)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  906. CHDIi010-A (#10c2 and CHDI-90002158)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  907. CHDIi011-A (#11c2 and CHDI-90002159)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  908. CHDIi013-A (#13c5 and CHDI-90002161)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  909. CHDIi014-A (#14c1 and CHDI-90002162)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  910. CHDIi016-A (#16c6 and CHDI-90002164)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  911. CHDIi017-A (#17c1 and CHDI-90002165)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  912. CHDIi018-A (#18c1 and CHDI-90002166)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  913. CHDIi019-A (#19c9 and CHDI-90002167)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  914. CHDIi020-A (#20c2 and CHDI-90002168)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  915. CHDIi021-A (#21c5 and CHDI-90002169)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  916. CHDIi022-A (#22c1 and CHDI-90002170)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  917. CHDIi023-A (#23c8 and CHDI-90002171)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  918. CHDIi024-A (#24c7 and CHDI-90002172)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  919. CHDIi026-A (#26c3 and CHDI-90002174)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  920. CHDIi027-A (#27c4 and CHDI-90002175)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  921. CHDIi028-A (#28c3 and CHDI-90002176)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  922. CHDIi029-A (#29c4 and CHDI-90002177)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  923. CHDIi031-A (#31c1 and CHDI-90002179)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  924. CHDIi033-A (#104c2 and CHDI-90002181)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  925. CHDIi034-A (#105c1 and CHDI-90002182)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  926. CHDIi035-A (#108c5 and CHDI-90002183)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  927. CHDIi036-A (#110c5 and CHDI-90002184)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  928. CHDIi038-A (#112c7 and CHDI-90002186)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  929. CHDIi040-A (#115c6 and CHDI-90002188)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  930. CHDIi041-A (#116c2 and CHDI-90002189)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  931. CHDIi042-A (#117c5 and CHDI-90002190)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  932. CHDIi043-A (#118c6 and CHDI-90002191)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  933. CHDIi044-A (#120c3 and CHDI-90002192)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  934. CHDIi045-A (#121c6 and CHDI-90002193)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  935. CHDIi046-A (#122c1 and CHDI-90002194)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  936. CHDIi047-A (#123c6 and CHDI-90002195)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  937. CHDIi048-A (#125c2 and CHDI-90002196)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  938. CHDIi049-A (#127c2 and CHDI-90002197)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  939. CHDIi050-A (#128c3 and CHDI-90002198)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  940. CHDIi051-A (#129c1 and CHDI-90002199)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  941. CHDIi054-A (#132c3 and CHDI-90002202)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  942. CHDIi055-A (#133c5 and CHDI-90002203)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  943. CHDIi056-A (#134c3 and CHDI-90002204)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  944. CHDTRi001-B (HT953B and iSP1.2.2B)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Cln3

  945. CHDTRi002-B (HT954B and iSP5.2.1B)

    United States Division of Translational Research, NICHD, NIH (CHDTR)

  946. CHDTRi003-A (HT955A and iSP5.2.2A)

    United States Division of Translational Research, NICHD, NIH (CHDTR)

  947. CHDTRi004-B (HT956B and iSP8.2.1B)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Cln3

  948. CHDTRi005-A (iSP10.2.1A and HT957A)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Cln3

  949. CHDTRi006-E (HT958E and iSP29.2.2E)

    United States Division of Translational Research, NICHD, NIH (CHDTR)

  950. CHINTAi001-A (iCON-001)

    India CHINTA (CHINTA)
    Disease:

    Normal (average)

  951. CHINTAi002-A (iCON-002)

    India CHINTA (CHINTA)
    Disease:

    Normal (average)

  952. CHOCi005-A

    United States CHOC Children's (CHOC)
    Disease:

    Gm1 gangliosidosis

  953. CHOPi001-A (CHOPJMML1854)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Juvenile myelomonocytic leukemia

  954. CHOPi005-A (LD0638.0A)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Hypomyelination with atrophy of basal ganglia and cerebellum

  955. CHOPi006-A (LD0313.0)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Hypomyelination with atrophy of basal ganglia and cerebellum

  956. CHOPi007-A

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Hypomyelination with atrophy of basal ganglia and cerebellum

  957. CHOPi008-A (TMD145.T21.G1S)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Transient abnormal myelopoiesis associated with down syndrome

  958. CHOPi008-B (TMD145.E46.G1S)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Transient abnormal myelopoiesis associated with down syndrome

  959. CHOPi008-C (DS145.T21.G1)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Transient abnormal myelopoiesis associated with down syndrome

  960. CHOPi012-A (CHOPACTG2-R257C)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Obsolete_megacystis-microcolon-intestinal hypoperistalsis syndrome 5

  961. CHOPi013-A (CHOPWT17_TPM1KOc28)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Normal (average)

  962. CHOPi014-A (CHOPWT15)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Normal (average)

  963. CHSUi001-A

    China Children’s Hospital Affiliated to Shandong University, (CHSU)
    Disease:

    Severe combined immunodeficiency

  964. CHSUi002-A

    China Children’s Hospital Affiliated to Shandong University, (CHSU)
    Disease:

    Hatipoglu immunodeficiency syndrome

  965. CHULAi001-A (GPDi001-A)

    Thailand Chulalongkorn University (CHULA)
    Disease:

    Glucose-6-phosphate dehydrogenase deficiency

  966. CHUQi001-A (522-2666-2 and SAMEA104271492)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Myotonic dystrophy type 1

  967. CHUQi002-A (ARSM44081223)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  968. CHUQi003-A (ARSM19061223)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  969. CHUQi004-A (ARSF50111122)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  970. CHUQi005-A (ARSF29170521)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  971. CHUQi006-A (ARSF31280521)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  972. CHUQi007-A (ARSM47280521)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  973. CHUQi008-A (ARSM42081221)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  974. CHUQi009-A (ARSF56190702)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  975. CHUQi010-A (ARSM50190702)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  976. CHUVi001-A

    Switzerland Centre Hospitalier Universitaire Vaudois (CHUV)
    Disease:

    Normal (average)

  977. CHWi001-A

    China The centre of prenatal diagnosis, The Central Hospital of Wenzhou (CHW)
    Disease:

    Intellectual disability

  978. CHZJUi001-A

    China Children’s Hospital (CHZJU)
    Disease:

    Dilated cardiomyopathy

  979. CIAUi002-C (UBC3 M1)

    Australia Centenary Institute of Cancer Medicine and Cell Biology (CIAU)
    Disease:

    Left bundle branch block

    Disease:

    Nonischemic cardiomyopathy

  980. CIAUi003-A (MCCIi005-A-1 and BFC4)

    Australia Centenary Institute of Cancer Medicine and Cell Biology (CIAU)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia 2

  981. 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

  982. CIBIOi007-A (P1C12_LDhiPSC_Laf)

    Italy Università degli Studi di Trento (CIBIO)
    Disease:

    Lafora disease

  983. 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)

  984. 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)

  985. CIMHi001-A (CIMHi44f028#4)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  986. CIMHi002-A (CIMHi29m067#3)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  987. CIMHi003-A (CIMHi23m035#2)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  988. CIMHi004-A (CIMHi24f007#4)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  989. CIMHi005-A (CIMHi25f100#5)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  990. CIMRi001-A (GM27291)

    United States Coriell Institute for Medical Research (CIMR)
    Disease:

    Vici syndrome

  991. CIPi001-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)
    Disease:

    Self-limited infantile epilepsy

  992. CIPi002-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)

  993. CIPi004-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)

  994. CIPi005-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  995. CIRAi005-A (F2KU1#4 and F2KU1)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  996. CIRAi005-A-1 (IsC2-F2KU1#4 and IsC-F2KU1)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  997. CIRAi006-A (F2KU2#17 and F2KU2)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  998. CIRAi006-A-1 (IsC-F2KU2 and IsC41-F2KU2#17)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  999. CIRMi001-A (CW13000)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1000. CIRMi002-A (CW13002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1001. CIRMi003-A (CW13003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1002. CIRMi004-A (CW13005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1003. CIRMi005-A (CW13006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1004. CIRMi006-A (CW13009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1005. CIRMi007-A (CW13011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1006. CIRMi008-A (CW13016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1007. CIRMi009-A (CW13017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1008. CIRMi010-A (CW13018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1009. CIRMi011-A (CW13020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1010. CIRMi012-A (CW13021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1011. CIRMi013-A (CW13023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1012. CIRMi014-A (CW13024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1013. CIRMi015-A (CW13025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1014. CIRMi016-A (CW13026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1015. CIRMi017-A (CW13028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1016. CIRMi018-A (CW13029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1017. CIRMi019-A (CW13030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1018. CIRMi020-A (CW13031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1019. CIRMi021-A (CW13032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1020. CIRMi022-A (CW13033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1021. CIRMi023-A (CW13034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1022. CIRMi024-A (CW13037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1023. CIRMi025-A (CW13038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1024. CIRMi026-A (CW13041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1025. CIRMi027-A (CW13042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1026. CIRMi028-A (CW13044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1027. CIRMi029-A (CW13045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1028. CIRMi030-A (CW13047)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1029. CIRMi031-A (CW13048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1030. CIRMi032-A (CW13049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1031. CIRMi033-A (CW13052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1032. CIRMi034-A (CW13053)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1033. CIRMi035-A (CW13055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1034. CIRMi036-A (CW13060)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1035. CIRMi037-A (CW13061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1036. CIRMi038-A (CW13063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1037. CIRMi039-A (CW13064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1038. CIRMi040-A (CW13065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1039. CIRMi041-A (CW13066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1040. CIRMi042-A (CW13067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1041. CIRMi043-A (CW13070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1042. CIRMi044-A (CW13072)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1043. CIRMi045-A (CW13073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1044. CIRMi046-A (CW13074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1045. CIRMi047-A (CW13075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1046. CIRMi048-A (CW13076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1047. CIRMi049-A (CW13077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1048. CIRMi050-A (CW13079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1049. CIRMi051-A (CW13088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1050. CIRMi052-A (CW13092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1051. CIRMi053-A (CW13093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1052. CIRMi054-A (CW13094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1053. CIRMi055-A (CW13095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1054. CIRMi056-A (CW13097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1055. CIRMi057-A (CW13098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1056. CIRMi058-A (CW13105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1057. CIRMi059-A (CW13107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1058. CIRMi060-A (CW13108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1059. CIRMi061-A (CW13109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1060. CIRMi062-A (CW13111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1061. CIRMi063-A (CW13112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1062. CIRMi064-A (CW13113)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1063. CIRMi065-A (CW13054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1064. CIRMi066-A (CW13069)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1065. CIRMi067-A (CW50049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1066. CIRMi068-A (CW50001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1067. CIRMi069-A (CW50005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1068. CIRMi070-A (CW50007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1069. CIRMi071-A (CW50010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1070. CIRMi072-A (CW50015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1071. CIRMi073-A (CW50017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1072. CIRMi074-A (CW50020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1073. CIRMi075-A (CW50030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1074. CIRMi076-A (CW50048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1075. CIRMi077-A (CW50057)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1076. CIRMi078-A (CW50077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1077. CIRMi079-A (CW50080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1078. CIRMi080-A (CW50081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1079. CIRMi081-A (CW50083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1080. CIRMi082-A (CW50084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1081. CIRMi083-A (CW50085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1082. CIRMi084-A (CW50087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1083. CIRMi085-A (CW50088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1084. CIRMi086-A (CW50089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1085. CIRMi087-A (CW50090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1086. CIRMi088-A (CW50091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1087. CIRMi089-A (CW50092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1088. CIRMi090-A (CW50100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1089. CIRMi091-A (CW50102)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1090. CIRMi092-A (CW50103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1091. CIRMi093-A (CW50105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1092. CIRMi094-A (CW50124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1093. CIRMi095-A (CW50125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1094. CIRMi096-A (CW50135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1095. CIRMi097-A (CW50140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1096. CIRMi098-A (CW50151)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1097. CIRMi099-A (CW50163)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1098. CIRMi100-A (CW50164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1099. CIRMi101-A (CW50002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1100. CIRMi102-A (CW50003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1101. CIRMi103-A (CW50004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1102. CIRMi104-A (CW50006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1103. CIRMi105-A (CW50008)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1104. CIRMi106-A (CW50009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1105. CIRMi107-A (CW50013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1106. CIRMi108-A (CW50016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1107. CIRMi109-A (CW50018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1108. CIRMi110-A (CW50019)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1109. CIRMi111-A (CW50021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1110. CIRMi112-A (CW50022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1111. CIRMi113-A (CW50023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1112. CIRMi114-A (CW50024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1113. CIRMi115-A (CW50025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1114. CIRMi116-A (CW50026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1115. CIRMi117-A (CW50027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1116. CIRMi118-A (CW50028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1117. CIRMi119-A (CW50029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1118. CIRMi120-A (CW50032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1119. CIRMi121-A (CW50033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1120. CIRMi122-A (CW50034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1121. CIRMi123-A (CW50035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1122. CIRMi124-A (CW50036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1123. CIRMi125-A (CW50037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1124. CIRMi126-A (CW50038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1125. CIRMi127-A (CW50039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1126. CIRMi128-A (CW50040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1127. CIRMi129-A (CW50041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1128. CIRMi130-A (CW50042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1129. CIRMi131-A (CW50043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1130. CIRMi132-A (CW50044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1131. CIRMi133-A (CW50045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1132. CIRMi134-A (CW50046)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1133. CIRMi135-A (CW50047)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1134. CIRMi136-A (CW50050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1135. CIRMi137-A (CW50051)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1136. CIRMi138-A (CW50052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1137. CIRMi139-A (CW50054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1138. CIRMi140-A (CW50055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1139. CIRMi141-A (CW50056)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1140. CIRMi142-A (CW50058)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1141. CIRMi143-A (CW50059)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1142. CIRMi144-A (CW50060)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1143. CIRMi145-A (CW50061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1144. CIRMi146-A (CW50062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1145. CIRMi147-A (CW50063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1146. CIRMi148-A (CW50064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1147. CIRMi149-A (CW50065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1148. CIRMi150-A (CW50066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1149. CIRMi151-A (CW50067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1150. CIRMi152-A (CW50068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1151. CIRMi153-A (CW50069)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1152. CIRMi154-A (CW50070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1153. CIRMi155-A (CW50071)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1154. CIRMi156-A (CW50072)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1155. CIRMi157-A (CW50073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1156. CIRMi158-A (CW50074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1157. CIRMi159-A (CW50075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1158. CIRMi160-A (CW50076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1159. CIRMi161-A (CW50078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1160. CIRMi162-A (CW50079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1161. CIRMi163-A (CW50082)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1162. CIRMi164-A (CW50086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1163. CIRMi165-A (CW50093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1164. CIRMi166-A (CW50094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1165. CIRMi167-A (CW50095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1166. CIRMi168-A (CW50096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1167. CIRMi169-A (CW50097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1168. CIRMi170-A (CW50099)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1169. CIRMi171-A (CW50101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1170. CIRMi172-A (CW50104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1171. CIRMi173-A (CW50106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1172. CIRMi174-A (CW50107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1173. CIRMi175-A (CW50108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1174. CIRMi176-A (CW50109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1175. CIRMi177-A (CW50111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1176. CIRMi178-A (CW50112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1177. CIRMi179-A (CW50113)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1178. CIRMi180-A (CW50114)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1179. CIRMi181-A (CW50115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1180. CIRMi182-A (CW50117)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1181. CIRMi183-A (CW50118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1182. CIRMi184-A (CW50119)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1183. CIRMi185-A (CW50120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1184. CIRMi186-A (CW50121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1185. CIRMi187-A (CW50122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1186. CIRMi188-A (CW50123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1187. CIRMi189-A (CW50126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1188. CIRMi190-A (CW50127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1189. CIRMi191-A (CW50128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1190. CIRMi192-A (CW50129)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1191. CIRMi193-A (CW50130)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1192. CIRMi194-A (CW50131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1193. CIRMi195-A (CW50132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1194. CIRMi196-A (CW50133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1195. CIRMi197-A (CW50134)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1196. CIRMi198-A (CW50136)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1197. CIRMi199-A (CW50137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1198. CIRMi200-A (CW50138)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1199. CIRMi201-A (CW50139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1200. CIRMi202-A (CW50141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1201. CIRMi203-A (CW50142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1202. CIRMi204-A (CW50143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1203. CIRMi205-A (CW50144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1204. CIRMi206-A (CW50145)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1205. CIRMi207-A (CW50147)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1206. CIRMi208-A (CW50148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1207. CIRMi209-A (CW50149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1208. CIRMi210-A (CW50150)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1209. CIRMi211-A (CW50152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1210. CIRMi212-A (CW50153)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1211. CIRMi213-A (CW50155)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1212. CIRMi214-A (CW50156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1213. CIRMi215-A (CW50157)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1214. CIRMi216-A (CW50158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1215. CIRMi217-A (CW50159)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1216. CIRMi218-A (CW50161)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1217. CIRMi219-A (CW50162)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1218. CIRMi220-A (CW50165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1219. CIRMi221-A (CW50166)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1220. CIRMi222-A (CW50167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1221. CIRMi223-A (CW50168)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1222. CIRMi224-A (CW50169)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1223. CIRMi225-A (CW50170)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1224. CIRMi226-A (CW50173)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1225. CIRMi227-A (CW50174)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1226. CIRMi228-A (CW50175)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1227. CIRMi229-A (CW50176)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1228. CIRMi230-A (CW50177)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  1229. CIRMi231-A (CW12000)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypoplasia of the optic nerve

  1230. CIRMi232-A (CW12001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1231. CIRMi233-A (CW12002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypoplasia of the optic nerve

  1232. CIRMi234-A (CW12003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1233. CIRMi235-A (CW12004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1234. CIRMi236-A (CW80003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1235. CIRMi237-A (CW80007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1236. CIRMi238-A (CW80008)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1237. CIRMi239-A (CW80009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1238. CIRMi240-A (CW80010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1239. CIRMi241-A (CW80011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1240. CIRMi242-A (CW80012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1241. CIRMi243-A (CW80014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1242. CIRMi244-A (CW80053)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1243. CIRMi245-A (CW80054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1244. CIRMi246-A (CW80018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1245. CIRMi247-A (CW80019)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1246. CIRMi248-A (CW80055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1247. CIRMi249-A (CW80021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1248. CIRMi250-A (CW80022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1249. CIRMi251-A (CW80024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1250. CIRMi252-A (CW80025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1251. CIRMi253-A (CW80026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1252. CIRMi254-A (CW80027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1253. CIRMi255-A (CW80028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1254. CIRMi256-A (CW80030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1255. CIRMi257-A (CW80031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1256. CIRMi258-A (CW80038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1257. CIRMi259-A (CW80040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1258. CIRMi260-A (CW80041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1259. CIRMi261-A (CW80042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1260. CIRMi262-A (CW80043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1261. CIRMi263-A (CW80044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1262. CIRMi264-A (CW80048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1263. CIRMi265-A (CW80049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  1264. CIRMi266-A (CW80050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1265. CIRMi267-A (CW70001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1266. CIRMi268-A (CW70002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1267. CIRMi269-A (CW70004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1268. CIRMi270-A (CW70005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1269. CIRMi271-A (CW70006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1270. CIRMi272-A (CW70007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1271. CIRMi273-A (CW70008)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1272. CIRMi274-A (CW70009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1273. CIRMi275-A (CW70011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1274. CIRMi276-A (CW70012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1275. CIRMi277-A (CW70013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1276. CIRMi278-A (CW70014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1277. CIRMi279-A (CW70015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1278. CIRMi280-A (CW70016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1279. CIRMi281-A (CW70017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1280. CIRMi282-A (CW70018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1281. CIRMi283-A (CW70019)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1282. CIRMi284-A (CW70021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1283. CIRMi285-A (CW70022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1284. CIRMi286-A (CW70028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1285. CIRMi287-A (CW70029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1286. CIRMi288-A (CW70030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1287. CIRMi289-A (CW70032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1288. CIRMi290-A (CW70033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1289. CIRMi291-A (CW70034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1290. CIRMi292-A (CW70035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1291. CIRMi293-A (CW70036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1292. CIRMi294-A (CW70037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1293. CIRMi295-A (CW70038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1294. CIRMi296-A (CW70039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1295. CIRMi297-A (CW70040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1296. CIRMi298-A (CW70041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1297. CIRMi299-A (CW70042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1298. CIRMi300-A (CW70043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1299. CIRMi301-A (CW70044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1300. CIRMi302-A (CW70045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1301. CIRMi303-A (CW70047)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1302. CIRMi304-A (CW70048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1303. CIRMi305-A (CW70049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1304. CIRMi306-A (CW70050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1305. CIRMi307-A (CW70052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1306. CIRMi308-A (CW70056)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1307. CIRMi309-A (CW70057)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1308. CIRMi310-A (CW70059)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1309. CIRMi311-A (CW70060)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetes mellitus

  1310. CIRMi312-A (CW70061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1311. CIRMi313-A (CW70063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinal vein occlusion

  1312. CIRMi314-A (CW70064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1313. CIRMi315-A (CW70066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1314. CIRMi316-A (CW70071)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1315. CIRMi317-A (CW70072)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1316. CIRMi318-A (CW70073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1317. CIRMi319-A (CW70075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1318. CIRMi320-A (CW70077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1319. CIRMi321-A (CW70079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1320. CIRMi322-A (CW70081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1321. CIRMi323-A (CW70085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1322. CIRMi324-A (CW70086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1323. CIRMi325-A (CW70087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1324. CIRMi326-A (CW70088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1325. CIRMi327-A (CW70089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1326. CIRMi328-A (CW70090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1327. CIRMi329-A (CW70091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1328. CIRMi330-A (CW70092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1329. CIRMi331-A (CW70093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1330. CIRMi332-A (CW70094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1331. CIRMi333-A (CW70096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1332. CIRMi334-A (CW70097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1333. CIRMi335-A (CW70098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1334. CIRMi336-A (CW70100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1335. CIRMi337-A (CW70101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1336. CIRMi338-A (CW70102)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1337. CIRMi339-A (CW70103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1338. CIRMi340-A (CW70104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1339. CIRMi341-A (CW70105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1340. CIRMi342-A (CW70106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1341. CIRMi343-A (CW70107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1342. CIRMi344-A (CW70108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1343. CIRMi345-A (CW70109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1344. CIRMi346-A (CW70110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1345. CIRMi347-A (CW70111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1346. CIRMi348-A (CW70112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1347. CIRMi349-A (CW70114)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1348. CIRMi350-A (CW70115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1349. CIRMi351-A (CW70116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1350. CIRMi352-A (CW70117)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1351. CIRMi353-A (CW70118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1352. CIRMi354-A (CW70120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1353. CIRMi355-A (CW70122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1354. CIRMi356-A (CW70123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1355. CIRMi357-A (CW70124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1356. CIRMi358-A (CW70125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1357. CIRMi359-A (CW70127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1358. CIRMi360-A (CW70128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1359. CIRMi361-A (CW70129)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1360. CIRMi362-A (CW70130)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1361. CIRMi363-A (CW70131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1362. CIRMi364-A (CW70132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1363. CIRMi365-A (CW70133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1364. CIRMi366-A (CW70134)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1365. CIRMi367-A (CW70135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1366. CIRMi368-A (CW70137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1367. CIRMi369-A (CW70138)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1368. CIRMi370-A (CW70140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1369. CIRMi371-A (CW70141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1370. CIRMi372-A (CW70142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1371. CIRMi373-A (CW70143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1372. CIRMi374-A (CW70144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1373. CIRMi375-A (CW70151)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1374. CIRMi376-A (CW70152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1375. CIRMi377-A (CW70155)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1376. CIRMi378-A (CW70156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1377. CIRMi379-A (CW70158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1378. CIRMi380-A (CW70160)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1379. CIRMi381-A (CW70161)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1380. CIRMi382-A (CW70164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1381. CIRMi383-A (CW70165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1382. CIRMi384-A (CW70167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1383. CIRMi385-A (CW70168)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1384. CIRMi386-A (CW70170)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1385. CIRMi387-A (CW70171)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1386. CIRMi388-A (CW70172)

    United States California Institute for Regenerative Medicine (CIRM)

  1387. CIRMi389-A (CW70173)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1388. CIRMi390-A (CW70174)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1389. CIRMi391-A (CW70175)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1390. CIRMi392-A (CW70176)

    United States California Institute for Regenerative Medicine (CIRM)

  1391. CIRMi393-A (CW70177)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1392. CIRMi394-A (CW70179)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1393. CIRMi395-A (CW70181)

    United States California Institute for Regenerative Medicine (CIRM)

  1394. CIRMi396-A (CW70182)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1395. CIRMi397-A (CW70010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1396. CIRMi398-A (CW70054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1397. CIRMi399-A (CW70055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1398. CIRMi400-A (CW70080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1399. CIRMi401-A (CW70184)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1400. CIRMi402-A (CW70185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1401. CIRMi403-A (CW70186)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1402. CIRMi404-A (CW70188)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1403. CIRMi405-A (CW70189)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1404. CIRMi406-A (CW70190)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1405. CIRMi407-A (CW70191)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinal detachment

  1406. CIRMi408-A (CW70193)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1407. CIRMi409-A (CW70194)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1408. CIRMi410-A (CW70195)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1409. CIRMi411-A (CW70196)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1410. CIRMi412-A (CW70197)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1411. CIRMi413-A (CW70198)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1412. CIRMi414-A (CW70201)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1413. CIRMi415-A (CW70203)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1414. CIRMi416-A (CW70205)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1415. CIRMi417-A (CW70206)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1416. CIRMi418-A (CW70207)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1417. CIRMi419-A (CW70208)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1418. CIRMi420-A (CW70210)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1419. CIRMi421-A (CW70211)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1420. CIRMi422-A (CW70212)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1421. CIRMi423-A (CW70213)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1422. CIRMi424-A (CW70214)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1423. CIRMi425-A (CW70215)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1424. CIRMi426-A (CW70216)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1425. CIRMi427-A (CW70217)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1426. CIRMi428-A (CW70219)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1427. CIRMi429-A (CW70221)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1428. CIRMi430-A (CW70224)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1429. CIRMi431-A (CW70225)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1430. CIRMi432-A (CW70226)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1431. CIRMi433-A (CW70229)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1432. CIRMi434-A (CW70230)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1433. CIRMi435-A (CW70232)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1434. CIRMi436-A (CW70233)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1435. CIRMi437-A (CW70235)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1436. CIRMi438-A (CW70239)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1437. CIRMi439-A (CW70240)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1438. CIRMi440-A (CW70241)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1439. CIRMi441-A (CW70244)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1440. CIRMi442-A (CW70245)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1441. CIRMi443-A (CW70246)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1442. CIRMi444-A (CW70247)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1443. CIRMi445-A (CW70248)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1444. CIRMi446-A (CW70249)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1445. CIRMi447-A (CW70250)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1446. CIRMi448-A (CW70251)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1447. CIRMi449-A (CW70252)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1448. CIRMi450-A (CW70253)

    United States California Institute for Regenerative Medicine (CIRM)

  1449. CIRMi451-A (CW70254)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1450. CIRMi452-A (CW70255)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1451. CIRMi453-A (CW70256)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1452. CIRMi454-A (CW70257)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1453. CIRMi455-A (CW70258)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1454. CIRMi456-A (CW70259)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1455. CIRMi457-A (CW70260)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1456. CIRMi458-A (CW70261)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1457. CIRMi459-A (CW70262)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1458. CIRMi460-A (CW70263)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1459. CIRMi461-A (CW70264)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1460. CIRMi462-A (CW70265)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1461. CIRMi463-A (CW70266)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1462. CIRMi464-A (CW70267)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1463. CIRMi465-A (CW70269)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1464. CIRMi466-A (CW70270)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1465. CIRMi467-A (CW70272)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1466. CIRMi468-A (CW70273)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  1467. CIRMi469-A (CW70274)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1468. CIRMi470-A (CW70275)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1469. CIRMi471-A (CW70276)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1470. CIRMi472-A (CW70278)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1471. CIRMi473-A (CW70279)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1472. CIRMi474-A (CW70280)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1473. CIRMi475-A (CW70281)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1474. CIRMi476-A (CW70282)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1475. CIRMi477-A (CW70283)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1476. CIRMi478-A (CW70284)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1477. CIRMi479-A (CW70286)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1478. CIRMi480-A (CW70287)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1479. CIRMi481-A (CW70289)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1480. CIRMi482-A (CW70290)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1481. CIRMi483-A (CW70292)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1482. CIRMi484-A (CW70296)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1483. CIRMi485-A (CW70297)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1484. CIRMi486-A (CW70298)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1485. CIRMi487-A (CW70299)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1486. CIRMi488-A (CW70300)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Achromatopsia

  1487. CIRMi489-A (CW70301)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1488. CIRMi490-A (CW70303)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1489. CIRMi491-A (CW70304)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1490. CIRMi492-A (CW70305)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1491. CIRMi493-A (CW70306)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1492. CIRMi494-A (CW70307)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1493. CIRMi495-A (CW70308)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1494. CIRMi496-A (CW70309)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1495. CIRMi497-A (CW70310)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1496. CIRMi498-A (CW70313)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1497. CIRMi499-A (CW70314)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1498. CIRMi500-A (CW70315)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1499. CIRMi501-A (CW70316)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1500. CIRMi502-A (CW70317)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1501. CIRMi503-A (CW70318)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1502. CIRMi504-A (CW70319)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Doyne honeycomb retinal dystrophy

  1503. CIRMi505-A (CW70320)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1504. CIRMi506-A (CW70321)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1505. CIRMi507-A (CW70322)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1506. CIRMi508-A (CW70323)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinitis pigmentosa

  1507. CIRMi509-A (CW70324)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1508. CIRMi510-A (CW70325)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1509. CIRMi511-A (CW70326)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  1510. CIRMi512-A (CW70327)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1511. CIRMi513-A (CW70330)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1512. CIRMi514-A (CW70332)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1513. CIRMi515-A (CW70337)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1514. CIRMi516-A (CW70338)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1515. CIRMi517-A (CW70339)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cataract

  1516. CIRMi518-A (CW70341)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1517. CIRMi519-A (CW70342)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinitis pigmentosa

  1518. CIRMi520-A (CW70343)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1519. CIRMi521-A (CW70344)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1520. CIRMi522-A (CW70345)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1521. CIRMi523-A (CW70346)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1522. CIRMi524-A (CW70347)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1523. CIRMi525-A (CW70348)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinitis pigmentosa

  1524. CIRMi526-A (CW70350)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1525. CIRMi527-A (CW70351)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1526. CIRMi528-A (CW70353)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1527. CIRMi529-A (CW70354)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1528. CIRMi530-A (CW70355)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1529. CIRMi531-A (CW70356)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinitis pigmentosa

  1530. CIRMi532-A (CW70358)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1531. CIRMi533-A (CW70359)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1532. CIRMi534-A (CW70363)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1533. CIRMi535-A (CW70364)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1534. CIRMi536-A (CW70366)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1535. CIRMi537-A (CW70368)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1536. CIRMi538-A (CW70369)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  1537. CIRMi539-A (CW70370)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1538. CIRMi540-A (CW70371)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1539. CIRMi541-A (CW70372)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  1540. CIRMi542-A (CW70373)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Retinitis pigmentosa

  1541. CIRMi543-A (CW70384)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  1542. CIRMi544-A (CW40002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1543. CIRMi545-A (CW40003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1544. CIRMi546-A (CW40004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1545. CIRMi547-A (CW40005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1546. CIRMi548-A (CW40006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1547. CIRMi549-A (CW40009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1548. CIRMi550-A (CW40010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1549. CIRMi551-A (CW40011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1550. CIRMi552-A (CW40012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1551. CIRMi553-A (CW40013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1552. CIRMi554-A (CW40014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1553. CIRMi555-A (CW40015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1554. CIRMi556-A (CW40017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1555. CIRMi557-A (CW40018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1556. CIRMi558-A (CW40020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1557. CIRMi559-A (CW40021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1558. CIRMi560-A (CW40022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1559. CIRMi561-A (CW40023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1560. CIRMi562-A (CW40024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1561. CIRMi563-A (CW40025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1562. CIRMi564-A (CW40026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1563. CIRMi565-A (CW40027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1564. CIRMi566-A (CW40028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1565. CIRMi567-A (CW40029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1566. CIRMi568-A (CW40030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1567. CIRMi569-A (CW40031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1568. CIRMi570-A (CW40032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1569. CIRMi571-A (CW40033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1570. CIRMi572-A (CW40034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1571. CIRMi573-A (CW40035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1572. CIRMi574-A (CW40037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1573. CIRMi575-A (CW40038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1574. CIRMi576-A (CW40039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1575. CIRMi577-A (CW40040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1576. CIRMi578-A (CW40042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1577. CIRMi579-A (CW40043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1578. CIRMi580-A (CW40044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1579. CIRMi581-A (CW40046)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1580. CIRMi582-A (CW40047)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1581. CIRMi583-A (CW40049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1582. CIRMi584-A (CW40051)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1583. CIRMi585-A (CW40052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1584. CIRMi586-A (CW40053)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1585. CIRMi587-A (CW40054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1586. CIRMi588-A (CW40055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1587. CIRMi589-A (CW40057)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1588. CIRMi590-A (CW40061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1589. CIRMi591-A (CW40062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1590. CIRMi592-A (CW40063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1591. CIRMi593-A (CW40064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1592. CIRMi594-A (CW40065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1593. CIRMi595-A (CW40066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1594. CIRMi596-A (CW40067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1595. CIRMi597-A (CW40068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1596. CIRMi598-A (CW40070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1597. CIRMi599-A (CW40071)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1598. CIRMi600-A (CW40073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1599. CIRMi601-A (CW40074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1600. CIRMi602-A (CW40075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1601. CIRMi603-A (CW40077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1602. CIRMi604-A (CW40078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1603. CIRMi605-A (CW40079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1604. CIRMi606-A (CW40080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1605. CIRMi607-A (CW40081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1606. CIRMi608-A (CW40083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1607. CIRMi609-A (CW40084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1608. CIRMi610-A (CW40085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1609. CIRMi611-A (CW40086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1610. CIRMi612-A (CW40087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1611. CIRMi613-A (CW40088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1612. CIRMi614-A (CW40089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1613. CIRMi615-A (CW40090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1614. CIRMi616-A (CW40091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1615. CIRMi617-A (CW40092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1616. CIRMi618-A (CW40094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1617. CIRMi619-A (CW40096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1618. CIRMi620-A (CW40097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1619. CIRMi621-A (CW40100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1620. CIRMi622-A (CW40101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1621. CIRMi623-A (CW40105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1622. CIRMi624-A (CW40106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1623. CIRMi625-A (CW40107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1624. CIRMi626-A (CW40109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1625. CIRMi627-A (CW40110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1626. CIRMi628-A (CW40111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1627. CIRMi629-A (CW40112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1628. CIRMi630-A (CW40113)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1629. CIRMi631-A (CW40114)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1630. CIRMi632-A (CW40115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1631. CIRMi633-A (CW40116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1632. CIRMi634-A (CW40118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1633. CIRMi635-A (CW40119)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1634. CIRMi636-A (CW40120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1635. CIRMi637-A (CW40121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1636. CIRMi638-A (CW40122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1637. CIRMi639-A (CW40123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1638. CIRMi640-A (CW40124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1639. CIRMi641-A (CW40125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1640. CIRMi642-A (CW40126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1641. CIRMi643-A (CW40127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1642. CIRMi644-A (CW40128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1643. CIRMi645-A (CW40129)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1644. CIRMi646-A (CW40131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1645. CIRMi647-A (CW40132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1646. CIRMi648-A (CW40135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1647. CIRMi649-A (CW40136)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1648. CIRMi650-A (CW40137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1649. CIRMi651-A (CW40139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1650. CIRMi652-A (CW40142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1651. CIRMi653-A (CW40144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1652. CIRMi654-A (CW40145)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1653. CIRMi655-A (CW40147)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1654. CIRMi656-A (CW40148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1655. CIRMi657-A (CW40149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1656. CIRMi658-A (CW40152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1657. CIRMi659-A (CW40153)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1658. CIRMi660-A (CW40157)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1659. CIRMi661-A (CW40159)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1660. CIRMi662-A (CW40160)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1661. CIRMi663-A (CW40161)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1662. CIRMi664-A (CW40163)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1663. CIRMi665-A (CW40164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1664. CIRMi666-A (CW40165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1665. CIRMi667-A (CW40167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1666. CIRMi668-A (CW40169)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1667. CIRMi669-A (CW40172)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1668. CIRMi670-A (CW40174)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1669. CIRMi671-A (CW40178)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1670. CIRMi672-A (CW40181)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1671. CIRMi673-A (CW40182)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1672. CIRMi674-A (CW40183)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1673. CIRMi675-A (CW40185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1674. CIRMi676-A (CW40187)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1675. CIRMi677-A (CW40190)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1676. CIRMi678-A (CW40191)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1677. CIRMi679-A (CW40192)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1678. CIRMi680-A (CW40193)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1679. CIRMi681-A (CW40194)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1680. CIRMi682-A (CW40195)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1681. CIRMi683-A (CW40196)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1682. CIRMi684-A (CW40197)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1683. CIRMi685-A (CW40198)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1684. CIRMi686-A (CW40199)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1685. CIRMi687-A (CW40200)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1686. CIRMi688-A (CW40201)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1687. CIRMi689-A (CW40206)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1688. CIRMi690-A (CW40207)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1689. CIRMi691-A (CW40208)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1690. CIRMi692-A (CW40209)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1691. CIRMi693-A (CW40211)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1692. CIRMi694-A (CW40212)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1693. CIRMi695-A (CW40213)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1694. CIRMi696-A (CW40214)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1695. CIRMi697-A (CW40217)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1696. CIRMi698-A (CW40218)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1697. CIRMi699-A (CW40219)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1698. CIRMi700-A (CW40220)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1699. CIRMi701-A (CW40221)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1700. CIRMi702-A (CW40222)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1701. CIRMi703-A (CW40224)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1702. CIRMi704-A (CW40225)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1703. CIRMi705-A (CW40226)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1704. CIRMi706-A (CW40227)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1705. CIRMi707-A (CW40228)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1706. CIRMi708-A (CW40229)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1707. CIRMi709-A (CW40230)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1708. CIRMi710-A (CW40231)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1709. CIRMi711-A (CW40232)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1710. CIRMi712-A (CW40233)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1711. CIRMi713-A (CW40234)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1712. CIRMi714-A (CW40235)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1713. CIRMi715-A (CW40236)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1714. CIRMi716-A (CW40237)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1715. CIRMi717-A (CW40239)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1716. CIRMi718-A (CW40243)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1717. CIRMi719-A (CW40244)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1718. CIRMi720-A (CW40245)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1719. CIRMi721-A (CW40246)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1720. CIRMi722-A (CW40247)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1721. CIRMi723-A (CW40249)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1722. CIRMi724-A (CW40250)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1723. CIRMi725-A (CW40251)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  1724. CIRMi726-A (CW30001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1725. CIRMi727-A (CW30002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1726. CIRMi728-A (CW30003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1727. CIRMi729-A (CW30004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1728. CIRMi730-A (CW30005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1729. CIRMi731-A (CW30006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1730. CIRMi732-A (CW30007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1731. CIRMi733-A (CW30008)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1732. CIRMi734-A (CW30009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1733. CIRMi735-A (CW30010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1734. CIRMi736-A (CW30011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1735. CIRMi737-A (CW30012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1736. CIRMi738-A (CW30014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1737. CIRMi739-A (CW30015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1738. CIRMi740-A (CW30016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1739. CIRMi741-A (CW30017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1740. CIRMi742-A (CW30018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1741. CIRMi743-A (CW30019)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1742. CIRMi744-A (CW30020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1743. CIRMi745-A (CW30022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1744. CIRMi746-A (CW30024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1745. CIRMi747-A (CW30027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1746. CIRMi748-A (CW30028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1747. CIRMi749-A (CW30029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1748. CIRMi750-A (CW30030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1749. CIRMi751-A (CW30031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1750. CIRMi752-A (CW30032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1751. CIRMi753-A (CW30033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1752. CIRMi754-A (CW30035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1753. CIRMi755-A (CW30036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1754. CIRMi756-A (CW30037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1755. CIRMi757-A (CW30038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1756. CIRMi758-A (CW30040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1757. CIRMi759-A (CW30042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1758. CIRMi760-A (CW30043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1759. CIRMi761-A (CW30044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1760. CIRMi762-A (CW30045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1761. CIRMi763-A (CW30046)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1762. CIRMi764-A (CW30048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1763. CIRMi765-A (CW30049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1764. CIRMi766-A (CW30050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1765. CIRMi767-A (CW30051)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1766. CIRMi768-A (CW30052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1767. CIRMi769-A (CW30053)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1768. CIRMi770-A (CW30054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1769. CIRMi771-A (CW30055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1770. CIRMi772-A (CW30056)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1771. CIRMi773-A (CW30058)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1772. CIRMi774-A (CW30059)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1773. CIRMi775-A (CW30060)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1774. CIRMi776-A (CW30061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1775. CIRMi777-A (CW30062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1776. CIRMi778-A (CW30063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1777. CIRMi779-A (CW30064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1778. CIRMi780-A (CW30065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1779. CIRMi781-A (CW30067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1780. CIRMi782-A (CW30068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1781. CIRMi783-A (CW30069)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1782. CIRMi784-A (CW30070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1783. CIRMi785-A (CW30071)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1784. CIRMi786-A (CW30073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1785. CIRMi787-A (CW30074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1786. CIRMi788-A (CW30075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1787. CIRMi789-A (CW30076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1788. CIRMi790-A (CW30077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1789. CIRMi791-A (CW30078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1790. CIRMi792-A (CW30079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1791. CIRMi793-A (CW30080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1792. CIRMi794-A (CW30081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1793. CIRMi795-A (CW30082)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1794. CIRMi796-A (CW30083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1795. CIRMi797-A (CW30084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1796. CIRMi798-A (CW30085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1797. CIRMi799-A (CW30086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1798. CIRMi800-A (CW30089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1799. CIRMi801-A (CW30090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1800. CIRMi802-A (CW30092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1801. CIRMi803-A (CW30093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  1802. CIRMi804-A (CW30094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1803. CIRMi805-A (CW30095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1804. CIRMi806-A (CW30096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1805. CIRMi807-A (CW30097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1806. CIRMi808-A (CW30098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1807. CIRMi809-A (CW30099)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1808. CIRMi810-A (CW30101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1809. CIRMi811-A (CW30102)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1810. CIRMi812-A (CW30103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1811. CIRMi813-A (CW30104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1812. CIRMi814-A (CW30105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1813. CIRMi815-A (CW30106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1814. CIRMi816-A (CW30107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1815. CIRMi817-A (CW30108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1816. CIRMi818-A (CW30109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1817. CIRMi819-A (CW30110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1818. CIRMi820-A (CW30111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1819. CIRMi821-A (CW30112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1820. CIRMi822-A (CW30113)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1821. CIRMi823-A (CW30115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1822. CIRMi824-A (CW30116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1823. CIRMi825-A (CW30119)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1824. CIRMi826-A (CW30120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1825. CIRMi827-A (CW30121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1826. CIRMi828-A (CW30122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1827. CIRMi829-A (CW30125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1828. CIRMi830-A (CW30126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1829. CIRMi831-A (CW30128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1830. CIRMi832-A (CW30130)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1831. CIRMi833-A (CW30131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1832. CIRMi834-A (CW30132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1833. CIRMi835-A (CW30133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1834. CIRMi836-A (CW30137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1835. CIRMi837-A (CW30138)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1836. CIRMi838-A (CW30139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1837. CIRMi839-A (CW30140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1838. CIRMi840-A (CW30141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1839. CIRMi841-A (CW30142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1840. CIRMi842-A (CW30143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1841. CIRMi843-A (CW30145)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1842. CIRMi844-A (CW30146)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1843. CIRMi845-A (CW30148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1844. CIRMi846-A (CW30149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  1845. CIRMi847-A (CW30151)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1846. CIRMi848-A (CW30152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1847. CIRMi849-A (CW30154)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1848. CIRMi850-A (CW30155)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1849. CIRMi851-A (CW30156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1850. CIRMi852-A (CW30157)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1851. CIRMi853-A (CW30158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1852. CIRMi854-A (CW30159)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1853. CIRMi855-A (CW30161)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1854. CIRMi856-A (CW30163)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1855. CIRMi857-A (CW30164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1856. CIRMi858-A (CW30165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1857. CIRMi859-A (CW30166)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1858. CIRMi860-A (CW30167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1859. CIRMi861-A (CW30168)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1860. CIRMi862-A (CW30169)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1861. CIRMi863-A (CW30170)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1862. CIRMi864-A (CW30171)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1863. CIRMi865-A (CW30172)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1864. CIRMi866-A (CW30174)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1865. CIRMi867-A (CW30175)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1866. CIRMi868-A (CW30176)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1867. CIRMi869-A (CW30177)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1868. CIRMi870-A (CW30178)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1869. CIRMi871-A (CW30179)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1870. CIRMi872-A (CW30180)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1871. CIRMi873-A (CW30181)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1872. CIRMi874-A (CW30182)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1873. CIRMi875-A (CW30184)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1874. CIRMi876-A (CW30185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1875. CIRMi877-A (CW30188)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1876. CIRMi878-A (CW30189)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1877. CIRMi879-A (CW30190)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1878. CIRMi880-A (CW30191)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1879. CIRMi881-A (CW30192)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1880. CIRMi882-A (CW30193)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1881. CIRMi883-A (CW30194)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1882. CIRMi884-A (CW30195)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1883. CIRMi885-A (CW30196)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1884. CIRMi886-A (CW30197)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1885. CIRMi887-A (CW30198)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1886. CIRMi888-A (CW30199)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1887. CIRMi889-A (CW30200)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1888. CIRMi890-A (CW30202)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1889. CIRMi891-A (CW30203)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1890. CIRMi892-A (CW30204)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1891. CIRMi893-A (CW30205)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1892. CIRMi894-A (CW30207)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1893. CIRMi895-A (CW30208)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1894. CIRMi896-A (CW30209)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1895. CIRMi897-A (CW30210)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  1896. CIRMi898-A (CW30211)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1897. CIRMi899-A (CW30212)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1898. CIRMi900-A (CW30213)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1899. CIRMi901-A (CW30214)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1900. CIRMi902-A (CW30215)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1901. CIRMi903-A (CW30216)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1902. CIRMi904-A (CW30219)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1903. CIRMi905-A (CW30220)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1904. CIRMi906-A (CW30221)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1905. CIRMi907-A (CW30222)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1906. CIRMi908-A (CW30223)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1907. CIRMi909-A (CW30224)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1908. CIRMi910-A (CW30225)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  1909. CIRMi911-A (CW30226)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1910. CIRMi912-A (CW30227)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1911. CIRMi913-A (CW30228)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1912. CIRMi914-A (CW30229)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1913. CIRMi915-A (CW30230)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1914. CIRMi916-A (CW30231)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1915. CIRMi917-A (CW30232)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1916. CIRMi918-A (CW30233)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1917. CIRMi919-A (CW30234)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1918. CIRMi920-A (CW30235)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1919. CIRMi921-A (CW30236)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1920. CIRMi922-A (CW30237)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1921. CIRMi923-A (CW30238)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1922. CIRMi924-A (CW30240)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1923. CIRMi925-A (CW30241)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1924. CIRMi926-A (CW30242)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1925. CIRMi927-A (CW30243)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1926. CIRMi928-A (CW30244)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1927. CIRMi929-A (CW30245)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1928. CIRMi930-A (CW30246)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1929. CIRMi931-A (CW30247)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1930. CIRMi932-A (CW30248)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1931. CIRMi933-A (CW30249)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1932. CIRMi934-A (CW30251)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1933. CIRMi935-A (CW30253)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1934. CIRMi936-A (CW30254)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1935. CIRMi937-A (CW30256)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1936. CIRMi938-A (CW30257)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1937. CIRMi939-A (CW30258)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1938. CIRMi940-A (CW30259)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1939. CIRMi941-A (CW30260)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1940. CIRMi942-A (CW30261)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1941. CIRMi943-A (CW30262)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1942. CIRMi944-A (CW30263)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1943. CIRMi945-A (CW30264)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1944. CIRMi946-A (CW30265)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1945. CIRMi947-A (CW30266)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1946. CIRMi948-A (CW30267)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1947. CIRMi949-A (CW30268)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1948. CIRMi950-A (CW30269)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1949. CIRMi951-A (CW30270)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1950. CIRMi952-A (CW30272)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1951. CIRMi953-A (CW30273)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1952. CIRMi954-A (CW30274)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1953. CIRMi955-A (CW30275)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1954. CIRMi956-A (CW30276)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1955. CIRMi957-A (CW30279)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1956. CIRMi958-A (CW30280)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1957. CIRMi959-A (CW30282)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1958. CIRMi960-A (CW30283)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1959. CIRMi961-A (CW30284)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1960. CIRMi962-A (CW30285)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1961. CIRMi963-A (CW30286)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1962. CIRMi964-A (CW30287)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1963. CIRMi965-A (CW30288)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1964. CIRMi966-A (CW30289)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Arrhythmogenic right ventricular dysplasia

  1965. CIRMi967-A (CW30290)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1966. CIRMi968-A (CW30291)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1967. CIRMi969-A (CW30292)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1968. CIRMi970-A (CW30293)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1969. CIRMi971-A (CW30295)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1970. CIRMi972-A (CW30297)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  1971. CIRMi973-A (CW30298)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1972. CIRMi974-A (CW30299)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1973. CIRMi975-A (CW30300)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1974. CIRMi976-A (CW30302)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1975. CIRMi977-A (CW30303)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1976. CIRMi978-A (CW30305)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1977. CIRMi979-A (CW30306)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1978. CIRMi980-A (CW30307)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1979. CIRMi981-A (CW30309)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1980. CIRMi982-A (CW30310)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1981. CIRMi983-A (CW30311)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1982. CIRMi984-A (CW30312)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1983. CIRMi985-A (CW30314)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1984. CIRMi986-A (CW30316)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1985. CIRMi987-A (CW30317)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1986. CIRMi988-A (CW30318)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  1987. CIRMi989-A (CW30319)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1988. CIRMi990-A (CW30320)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1989. CIRMi991-A (CW30321)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1990. CIRMi992-A (CW30322)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1991. CIRMi993-A (CW30323)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1992. CIRMi994-A (CW30324)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1993. CIRMi995-A (CW30325)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1994. CIRMi996-A (CW30326)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1995. CIRMi997-A (CW30327)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1996. CIRMi998-A (CW30328)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  1997. CIRMi999-A (CW30329)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1998. CIRMi00A-A (CW30331)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  1999. CIRMi00B-A (CW30332)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2000. CIRMi00C-A (CW30333)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2001. CIRMi00D-A (CW30334)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2002. CIRMi00E-A (CW30335)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2003. CIRMi00F-A (CW30336)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2004. CIRMi00G-A (CW30337)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2005. CIRMi00H-A (CW30338)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2006. CIRMi00I-A (CW30339)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2007. CIRMi00J-A (CW30340)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2008. CIRMi00K-A (CW30342)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2009. CIRMi00L-A (CW30343)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2010. CIRMi00M-A (CW30344)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2011. CIRMi00N-A (CW30345)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2012. CIRMi00O-A (CW30346)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2013. CIRMi00P-A (CW30348)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2014. CIRMi00Q-A (CW30349)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2015. CIRMi00R-A (CW30350)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2016. CIRMi00S-A (CW30353)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2017. CIRMi00T-A (CW30354)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2018. CIRMi00U-A (CW30355)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2019. CIRMi00V-A (CW30356)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2020. CIRMi00W-A (CW30357)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2021. CIRMi00X-A (CW30358)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2022. CIRMi00Y-A (CW30359)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  2023. CIRMi00Z-A (CW30360)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2024. CIRMi01A-A (CW30361)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2025. CIRMi01B-A (CW30362)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2026. CIRMi01C-A (CW30363)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2027. CIRMi01D-A (CW30364)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2028. CIRMi01E-A (CW30369)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2029. CIRMi01F-A (CW30370)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2030. CIRMi01G-A (CW30371)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2031. CIRMi01H-A (CW30374)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2032. CIRMi01I-A (CW30376)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2033. CIRMi01J-A (CW30380)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2034. CIRMi01K-A (CW30382)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2035. CIRMi01L-A (CW30383)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2036. CIRMi01M-A (CW30386)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2037. CIRMi01N-A (CW30387)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2038. CIRMi01O-A (CW30389)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2039. CIRMi01P-A (CW30390)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2040. CIRMi01Q-A (CW30391)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2041. CIRMi01R-A (CW30392)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2042. CIRMi01S-A (CW30393)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2043. CIRMi01T-A (CW30394)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2044. CIRMi01U-A (CW30395)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2045. CIRMi01V-A (CW30397)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2046. CIRMi01W-A (CW30398)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2047. CIRMi01X-A (CW30399)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2048. CIRMi01Y-A (CW30400)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2049. CIRMi01Z-A (CW30401)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2050. CIRMi02A-A (CW30403)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2051. CIRMi02B-A (CW30404)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2052. CIRMi02C-A (CW30406)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2053. CIRMi02D-A (CW30408)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2054. CIRMi02E-A (CW30409)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2055. CIRMi02F-A (CW30410)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2056. CIRMi02G-A (CW30412)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2057. CIRMi02H-A (CW30413)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2058. CIRMi02I-A (CW30414)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2059. CIRMi02J-A (CW30415)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2060. CIRMi02K-A (CW30417)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2061. CIRMi02L-A (CW30418)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2062. CIRMi02M-A (CW30419)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2063. CIRMi02N-A (CW30420)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2064. CIRMi02O-A (CW30421)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2065. CIRMi02P-A (CW30422)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2066. CIRMi02Q-A (CW30423)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2067. CIRMi02R-A (CW30425)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2068. CIRMi02S-A (CW30426)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2069. CIRMi02T-A (CW30427)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2070. CIRMi02U-A (CW30428)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2071. CIRMi02V-A (CW30429)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  2072. CIRMi02W-A (CW30430)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2073. CIRMi02X-A (CW30431)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2074. CIRMi02Y-A (CW30432)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2075. CIRMi02Z-A (CW30433)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Arrhythmogenic right ventricular dysplasia

  2076. CIRMi03A-A (CW30434)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2077. CIRMi03B-A (CW30435)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2078. CIRMi03C-A (CW30436)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2079. CIRMi03D-A (CW30437)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2080. CIRMi03E-A (CW30438)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2081. CIRMi03F-A (CW30439)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2082. CIRMi03G-A (CW30440)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2083. CIRMi03H-A (CW30441)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2084. CIRMi03I-A (CW30442)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2085. CIRMi03J-A (CW30443)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2086. CIRMi03K-A (CW30444)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2087. CIRMi03L-A (CW30445)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2088. CIRMi03M-A (CW30446)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2089. CIRMi03N-A (CW30447)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2090. CIRMi03O-A (CW30448)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2091. CIRMi03P-A (CW30449)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2092. CIRMi03Q-A (CW30450)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2093. CIRMi03R-A (CW30452)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2094. CIRMi03S-A (CW30453)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2095. CIRMi03T-A (CW30454)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2096. CIRMi03U-A (CW30455)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2097. CIRMi03V-A (CW30456)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2098. CIRMi03W-A (CW30457)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2099. CIRMi03X-A (CW30459)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2100. CIRMi03Y-A (CW30460)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2101. CIRMi03Z-A (CW30461)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2102. CIRMi04A-A (CW30462)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2103. CIRMi04B-A (CW30463)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2104. CIRMi04C-A (CW30464)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2105. CIRMi04D-A (CW30465)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2106. CIRMi04E-A (CW30466)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2107. CIRMi04F-A (CW30467)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2108. CIRMi04G-A (CW30468)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2109. CIRMi04H-A (CW30470)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2110. CIRMi04I-A (CW30471)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2111. CIRMi04J-A (CW30472)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2112. CIRMi04K-A (CW30473)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2113. CIRMi04L-A (CW30474)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2114. CIRMi04M-A (CW30476)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2115. CIRMi04N-A (CW30477)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2116. CIRMi04O-A (CW30478)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2117. CIRMi04P-A (CW30479)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2118. CIRMi04Q-A (CW30480)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  2119. CIRMi04R-A (CW30481)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2120. CIRMi04S-A (CW30482)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2121. CIRMi04T-A (CW30483)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2122. CIRMi04U-A (CW30484)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Restrictive cardiomyopathy

  2123. CIRMi04V-A (CW30485)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  2124. CIRMi04W-A (CW30486)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2125. CIRMi04X-A (CW30488)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2126. CIRMi04Y-A (CW30489)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2127. CIRMi04Z-A (CW30490)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2128. CIRMi05A-A (CW30491)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2129. CIRMi05B-A (CW30492)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2130. CIRMi05C-A (CW30494)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2131. CIRMi05D-A (CW30495)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2132. CIRMi05E-A (CW30496)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2133. CIRMi05F-A (CW30497)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2134. CIRMi05G-A (CW30499)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2135. CIRMi05H-A (CW30500)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2136. CIRMi05I-A (CW30501)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2137. CIRMi05J-A (CW30503)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2138. CIRMi05K-A (CW30505)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2139. CIRMi05L-A (CW30506)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2140. CIRMi05M-A (CW30508)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2141. CIRMi05N-A (CW30509)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2142. CIRMi05O-A (CW30510)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2143. CIRMi05P-A (CW30512)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2144. CIRMi05Q-A (CW30513)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2145. CIRMi05R-A (CW30515)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2146. CIRMi05S-A (CW30516)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2147. CIRMi05T-A (CW30519)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2148. CIRMi05U-A (CW30520)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  2149. CIRMi05V-A (CW30522)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2150. CIRMi05W-A (CW30523)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2151. CIRMi05X-A (CW30525)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2152. CIRMi05Y-A (CW30526)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2153. CIRMi05Z-A (CW30527)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2154. CIRMi06A-A (CW30528)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2155. CIRMi06B-A (CW30529)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  2156. CIRMi06C-A (CW10001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2157. CIRMi06D-A (CW10002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2158. CIRMi06E-A (CW10003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2159. CIRMi06F-A (CW10004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2160. CIRMi06G-A (CW10005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2161. CIRMi06H-A (CW10007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2162. CIRMi06I-A (CW10009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2163. CIRMi06J-A (CW10010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2164. CIRMi06K-A (CW10011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2165. CIRMi06L-A (CW10012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2166. CIRMi06M-A (CW10013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2167. CIRMi06N-A (CW10014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2168. CIRMi06O-A (CW10015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatic steatosis

  2169. CIRMi06P-A (CW10018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2170. CIRMi06Q-A (CW10020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2171. CIRMi06R-A (CW10021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2172. CIRMi06S-A (CW10023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2173. CIRMi06T-A (CW10024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2174. CIRMi06U-A (CW10025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2175. CIRMi06V-A (CW10026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2176. CIRMi06W-A (CW10027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2177. CIRMi06X-A (CW10030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2178. CIRMi06Y-A (CW10033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2179. CIRMi06Z-A (CW10034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2180. CIRMi07A-A (CW10035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2181. CIRMi07B-A (CW10036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2182. CIRMi07C-A (CW10037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2183. CIRMi07D-A (CW10038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2184. CIRMi07E-A (CW10039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2185. CIRMi07F-A (CW10040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2186. CIRMi07G-A (CW10041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2187. CIRMi07H-A (CW10042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2188. CIRMi07I-A (CW10044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2189. CIRMi07J-A (CW10045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2190. CIRMi07K-A (CW10050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2191. CIRMi07L-A (CW10054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2192. CIRMi07M-A (CW10058)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2193. CIRMi07N-A (CW10060)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2194. CIRMi07O-A (CW10061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2195. CIRMi07P-A (CW10062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2196. CIRMi07Q-A (CW10063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2197. CIRMi07R-A (CW10064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2198. CIRMi07S-A (CW10066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2199. CIRMi07T-A (CW10067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2200. CIRMi07U-A (CW10068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2201. CIRMi07V-A (CW10069)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2202. CIRMi07W-A (CW10073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2203. CIRMi07X-A (CW10074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2204. CIRMi07Y-A (CW10075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2205. CIRMi07Z-A (CW10076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2206. CIRMi08A-A (CW10077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2207. CIRMi08B-A (CW10078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2208. CIRMi08C-A (CW10079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2209. CIRMi08D-A (CW10081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2210. CIRMi08E-A (CW10083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2211. CIRMi08F-A (CW10084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2212. CIRMi08G-A (CW10085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2213. CIRMi08H-A (CW10086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2214. CIRMi08I-A (CW10087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2215. CIRMi08J-A (CW10088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2216. CIRMi08K-A (CW10089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2217. CIRMi08L-A (CW10090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2218. CIRMi08M-A (CW10091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2219. CIRMi08N-A (CW10093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2220. CIRMi08O-A (CW10094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2221. CIRMi08P-A (CW10095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2222. CIRMi08Q-A (CW10096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2223. CIRMi08R-A (CW10097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2224. CIRMi08S-A (CW10098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2225. CIRMi08T-A (CW10100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2226. CIRMi08U-A (CW10101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2227. CIRMi08V-A (CW10102)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2228. CIRMi08W-A (CW10103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2229. CIRMi08X-A (CW10104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2230. CIRMi08Y-A (CW10107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2231. CIRMi08Z-A (CW10109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2232. CIRMi09A-A (CW10110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2233. CIRMi09B-A (CW10111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2234. CIRMi09C-A (CW10114)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2235. CIRMi09D-A (CW10115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2236. CIRMi09E-A (CW10116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2237. CIRMi09F-A (CW10118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2238. CIRMi09G-A (CW10120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2239. CIRMi09H-A (CW10121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2240. CIRMi09I-A (CW10122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2241. CIRMi09J-A (CW10126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2242. CIRMi09K-A (CW10127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2243. CIRMi09L-A (CW10128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2244. CIRMi09M-A (CW10130)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2245. CIRMi09N-A (CW10131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2246. CIRMi09O-A (CW10133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2247. CIRMi09P-A (CW10135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2248. CIRMi09Q-A (CW10136)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2249. CIRMi09R-A (CW10137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2250. CIRMi09S-A (CW10139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2251. CIRMi09T-A (CW10141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2252. CIRMi09U-A (CW10142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2253. CIRMi09V-A (CW10143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2254. CIRMi09W-A (CW10144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2255. CIRMi09X-A (CW10146)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2256. CIRMi09Y-A (CW10147)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2257. CIRMi09Z-A (CW10148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2258. CIRMi10A-A (CW10149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2259. CIRMi10B-A (CW10150)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2260. CIRMi10C-A (CW10152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2261. CIRMi10D-A (CW10153)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2262. CIRMi10E-A (CW10154)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2263. CIRMi10F-A (CW10155)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2264. CIRMi10G-A (CW10156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2265. CIRMi10H-A (CW10157)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2266. CIRMi10I-A (CW10158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2267. CIRMi10J-A (CW10159)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2268. CIRMi10K-A (CW10160)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2269. CIRMi10L-A (CW10162)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2270. CIRMi10M-A (CW10163)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2271. CIRMi10N-A (CW10165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2272. CIRMi10O-A (CW10166)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2273. CIRMi10P-A (CW10167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2274. CIRMi10Q-A (CW10168)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2275. CIRMi10R-A (CW10169)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2276. CIRMi10S-A (CW10171)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2277. CIRMi10T-A (CW10172)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2278. CIRMi10U-A (CW10173)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2279. CIRMi10V-A (CW10175)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2280. CIRMi10W-A (CW10176)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2281. CIRMi10X-A (CW10177)

    United States California Institute for Regenerative Medicine (CIRM)

  2282. CIRMi10Y-A (CW10178)

    United States California Institute for Regenerative Medicine (CIRM)

  2283. CIRMi10Z-A (CW10181)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2284. CIRMi11A-A (CW10182)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2285. CIRMi11B-A (CW10183)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2286. CIRMi11C-A (CW10184)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatic steatosis

  2287. CIRMi11D-A (CW10185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2288. CIRMi11E-A (CW10186)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2289. CIRMi11F-A (CW10187)

    United States California Institute for Regenerative Medicine (CIRM)

  2290. CIRMi11G-A (CW10188)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2291. CIRMi11H-A (CW10189)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2292. CIRMi11I-A (CW10190)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2293. CIRMi11J-A (CW10191)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2294. CIRMi11K-A (CW10192)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2295. CIRMi11L-A (CW10201)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2296. CIRMi11M-A (CW10202)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2297. CIRMi11N-A (CW10203)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2298. CIRMi11O-A (CW10205)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  2299. CIRMi11P-A (CW10206)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2300. CIRMi11Q-A (CW10208)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  2301. CIRMi11R-A (CW60314)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2302. CIRMi11S-A (CW60441)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2303. CIRMi11T-A (CW60520)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2304. CIRMi11U-A (CW11000)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2305. CIRMi11V-A (CW11001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2306. CIRMi11W-A (CW11004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2307. CIRMi11X-A (CW11005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2308. CIRMi11Y-A (CW11006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2309. CIRMi11Z-A (CW11009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2310. CIRMi12A-A (CW11012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2311. CIRMi12B-A (CW11013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2312. CIRMi12C-A (CW11015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2313. CIRMi12D-A (CW11016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2314. CIRMi12E-A (CW11018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2315. CIRMi12F-A (CW11019)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2316. CIRMi12G-A (CW11030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2317. CIRMi12H-A (CW11031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2318. CIRMi12I-A (CW11032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2319. CIRMi12J-A (CW11033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2320. CIRMi12K-A (CW11034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2321. CIRMi12L-A (CW11036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2322. CIRMi12M-A (CW11040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2323. CIRMi12N-A (CW11041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2324. CIRMi12O-A (CW11042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2325. CIRMi12P-A (CW11043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2326. CIRMi12Q-A (CW11046)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2327. CIRMi12R-A (CW11072)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2328. CIRMi12S-A (CW11074)

    United States California Institute for Regenerative Medicine (CIRM)

  2329. CIRMi12T-A (CW11075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2330. CIRMi12U-A (CW11077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2331. CIRMi12V-A (CW11078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2332. CIRMi12W-A (CW11079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2333. CIRMi12X-A (CW11090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2334. CIRMi12Y-A (CW11091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2335. CIRMi12Z-A (CW11093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2336. CIRMi13A-A (CW11094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2337. CIRMi13B-A (CW11096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2338. CIRMi13C-A (CW11098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2339. CIRMi13D-A (CW11100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2340. CIRMi13E-A (CW11101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2341. CIRMi13F-A (CW11110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2342. CIRMi13G-A (CW11119)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2343. CIRMi13H-A (CW11120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2344. CIRMi13I-A (CW11121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2345. CIRMi13J-A (CW11122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2346. CIRMi13K-A (CW11123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2347. CIRMi13L-A (CW11124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2348. CIRMi13M-A (CW11125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2349. CIRMi13N-A (CW11126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2350. CIRMi13O-A (CW11127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2351. CIRMi13P-A (CW11132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2352. CIRMi13Q-A (CW11133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2353. CIRMi13R-A (CW11140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2354. CIRMi13S-A (CW11141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  2355. CIRMi13T-A (CW11147)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2356. CIRMi13U-A (CW11148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2357. CIRMi13V-A (CW11150)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  2358. CIRMi13W-A (CW20001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2359. CIRMi13X-A (CW20002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2360. CIRMi13Y-A (CW20004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2361. CIRMi13Z-A (CW20006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2362. CIRMi14A-A (CW20008)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2363. CIRMi14B-A (CW20009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2364. CIRMi14C-A (CW20012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2365. CIRMi14D-A (CW20015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2366. CIRMi14E-A (CW20016)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2367. CIRMi14F-A (CW20020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2368. CIRMi14G-A (CW20021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2369. CIRMi14H-A (CW20023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2370. CIRMi14I-A (CW20025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2371. CIRMi14J-A (CW20026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2372. CIRMi14K-A (CW20027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2373. CIRMi14L-A (CW20029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2374. CIRMi14M-A (CW20030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2375. CIRMi14N-A (CW20031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2376. CIRMi14O-A (CW20032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2377. CIRMi14P-A (CW20033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2378. CIRMi14Q-A (CW20034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2379. CIRMi14R-A (CW20035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2380. CIRMi14S-A (CW20039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2381. CIRMi14T-A (CW20041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2382. CIRMi14U-A (CW20042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2383. CIRMi14V-A (CW20043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2384. CIRMi14W-A (CW20044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2385. CIRMi14X-A (CW20046)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2386. CIRMi14Y-A (CW20047)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2387. CIRMi14Z-A (CW20048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2388. CIRMi15A-A (CW20049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2389. CIRMi15B-A (CW20050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2390. CIRMi15C-A (CW20051)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2391. CIRMi15D-A (CW20052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2392. CIRMi15E-A (CW20053)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2393. CIRMi15F-A (CW20054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2394. CIRMi15G-A (CW20055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2395. CIRMi15H-A (CW20056)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2396. CIRMi15I-A (CW20057)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2397. CIRMi15J-A (CW20058)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2398. CIRMi15K-A (CW20061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2399. CIRMi15L-A (CW20062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2400. CIRMi15M-A (CW20063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2401. CIRMi15N-A (CW20065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2402. CIRMi15O-A (CW20068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2403. CIRMi15P-A (CW20069)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2404. CIRMi15Q-A (CW20070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2405. CIRMi15R-A (CW20073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2406. CIRMi15S-A (CW20074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2407. CIRMi15T-A (CW20075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2408. CIRMi15U-A (CW20076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2409. CIRMi15V-A (CW20077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2410. CIRMi15W-A (CW20078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2411. CIRMi15X-A (CW20079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2412. CIRMi15Y-A (CW20080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2413. CIRMi15Z-A (CW20081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2414. CIRMi16A-A (CW20083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2415. CIRMi16B-A (CW20084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2416. CIRMi16C-A (CW20085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2417. CIRMi16D-A (CW20087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2418. CIRMi16E-A (CW20088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2419. CIRMi16F-A (CW20091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2420. CIRMi16G-A (CW20092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2421. CIRMi16H-A (CW20094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2422. CIRMi16I-A (CW20095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2423. CIRMi16J-A (CW20098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2424. CIRMi16K-A (CW20099)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2425. CIRMi16L-A (CW20100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2426. CIRMi16M-A (CW20101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2427. CIRMi16N-A (CW20103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2428. CIRMi16O-A (CW20104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2429. CIRMi16P-A (CW20105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2430. CIRMi16Q-A (CW20106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2431. CIRMi16R-A (CW20107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2432. CIRMi16S-A (CW20108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2433. CIRMi16T-A (CW20109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2434. CIRMi16U-A (CW20110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2435. CIRMi16V-A (CW20111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2436. CIRMi16W-A (CW20112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2437. CIRMi16X-A (CW20115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2438. CIRMi16Y-A (CW20116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2439. CIRMi16Z-A (CW20118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2440. CIRMi17A-A (CW20121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2441. CIRMi17B-A (CW20122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2442. CIRMi17C-A (CW20123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2443. CIRMi17D-A (CW20124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2444. CIRMi17E-A (CW20125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2445. CIRMi17F-A (CW20126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2446. CIRMi17G-A (CW20128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2447. CIRMi17H-A (CW20129)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2448. CIRMi17I-A (CW20131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2449. CIRMi17J-A (CW20132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2450. CIRMi17K-A (CW20133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2451. CIRMi17L-A (CW20135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2452. CIRMi17M-A (CW20136)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2453. CIRMi17N-A (CW20137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2454. CIRMi17O-A (CW20139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2455. CIRMi17P-A (CW20140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2456. CIRMi17Q-A (CW20141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2457. CIRMi17R-A (CW20142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2458. CIRMi17S-A (CW20144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2459. CIRMi17T-A (CW20146)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2460. CIRMi17U-A (CW20149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2461. CIRMi17V-A (CW20150)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2462. CIRMi17W-A (CW20151)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2463. CIRMi17X-A (CW20152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2464. CIRMi17Y-A (CW20153)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2465. CIRMi17Z-A (CW20156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2466. CIRMi18A-A (CW20158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2467. CIRMi18B-A (CW20164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2468. CIRMi18C-A (CW20166)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2469. CIRMi18D-A (CW20167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2470. CIRMi18E-A (CW20170)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2471. CIRMi18F-A (CW20178)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2472. CIRMi18G-A (CW20179)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2473. CIRMi18H-A (CW20181)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2474. CIRMi18I-A (CW20183)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2475. CIRMi18J-A (CW20184)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2476. CIRMi18K-A (CW20185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2477. CIRMi18L-A (CW20186)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2478. CIRMi18M-A (CW20188)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2479. CIRMi18N-A (CW20192)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2480. CIRMi18O-A (CW20193)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2481. CIRMi18P-A (CW20195)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2482. CIRMi18Q-A (CW20196)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2483. CIRMi18R-A (CW20200)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2484. CIRMi18S-A (CW20201)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2485. CIRMi18T-A (CW20202)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2486. CIRMi18U-A (CW20203)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2487. CIRMi18V-A (CW20204)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2488. CIRMi18W-A (CW20206)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2489. CIRMi18X-A (CW20207)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2490. CIRMi18Y-A (CW20209)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2491. CIRMi18Z-A (CW20210)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2492. CIRMi19A-A (CW20212)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2493. CIRMi19B-A (CW20213)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2494. CIRMi19C-A (CW20214)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2495. CIRMi19D-A (CW20222)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2496. CIRMi19E-A (CW20225)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2497. CIRMi19F-A (CW20226)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2498. CIRMi19G-A (CW20231)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2499. CIRMi19H-A (CW20235)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2500. CIRMi19I-A (CW20237)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2501. CIRMi19J-A (CW20239)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2502. CIRMi19K-A (CW20240)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2503. CIRMi19L-A (CW20242)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2504. CIRMi19M-A (CW20243)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2505. CIRMi19N-A (CW20245)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2506. CIRMi19O-A (CW20249)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2507. CIRMi19P-A (CW20252)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2508. CIRMi19Q-A (CW20273)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2509. CIRMi19R-A (CW20277)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2510. CIRMi19S-A (CW20278)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2511. CIRMi19T-A (CW20284)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2512. CIRMi19U-A (CW20295)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2513. CIRMi19V-A (CW20296)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2514. CIRMi19W-A (CW20299)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2515. CIRMi19X-A (CW20300)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2516. CIRMi19Y-A (CW20303)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2517. CIRMi19Z-A (CW20311)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2518. CIRMi20A-A (CW20320)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2519. CIRMi20B-A (CW20321)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2520. CIRMi20C-A (CW20322)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2521. CIRMi20D-A (CW20323)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2522. CIRMi20E-A (CW20324)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2523. CIRMi20F-A (CW20325)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2524. CIRMi20G-A (CW20326)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  2525. CIRMi20H-A (CW60040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2526. CIRMi20I-A (CW60109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  2527. CMCi001-A (CMC-KIN-hiPSC)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Karyomegalic interstitial nephritis

  2528. UCSFi001-A-78 (WTC11-KL-GFP)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Healthy

  2529. UCSFi001-A-82 (WTC11-SLC12A3)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Gitelman syndrome

  2530. CMCi002-A (CMC-GIT-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Gitelman syndrome

  2531. CMCi006-A (CMC-Fb-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

  2532. CMCi006-A-1 (CMC-Fb001(A4GALT-KO))

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

  2533. CMCi007-A (CMC-Fb-004)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

  2534. CMCi009-A (CMC-BHD-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Birt-hogg-dube syndrome

  2535. CMCi010-A (CMC-Fb-002)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

  2536. CMCi011-A (CMC-DENT-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Dent disease

  2537. CMDi001-A (01016)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  2538. CMDi002-A (01173)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  2539. CMDi003-A (01174)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  2540. CMDi004-A (01175)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  2541. CMDi005-A (01176)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  2542. CMGANTi003-A (SEMD1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  2543. CMGANTi004-A (SEMD2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  2544. CMGANTi005-A (iPSC_MFS_FBN1_MCE-KB_C8)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Marfan syndrome

  2545. CMGANTi006-A (SEDC1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Spondyloepiphyseal dysplasia congenita

  2546. CMGANTi007-A (SEDC2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Spondyloepiphyseal dysplasia congenita

  2547. CMGANTi008-A (iPSC_MFS_FBN1_Fi930129_C8)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Marfan syndrome

  2548. CMUi002-A

    China Capital Medical University (CMU)
    Disease:

    Normal (average)

  2549. CMUi002-A-1 (NONO-KO-iPSCs)

    China Capital Medical University (CMU)
    Disease:

    Left ventricular noncompaction cardiomyopathy

    Disease:

    Mental retardation

  2550. CPGHi004-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal (average)

  2551. CPGHi006-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Autosomal dominant polycystic kidney disease

  2552. CPGHi007-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal (average)

  2553. CPGHi008-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Autosomal recessive polycystic kidney disease

  2554. CRICKi001-A (iFCI001)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Intellectual disability

  2555. CRICKi002-A (iFCI027)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Intellectual disability

  2556. CRICKi003-A (iFCI002)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Intellectual disability

  2557. CRICKi004-A (iFCI008)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Spinal muscular atrophy with lower extremity predominant

  2558. CRICKi005-A (iFCI004)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Spinal muscular atrophy

  2559. CRICKi006-A (iFCI005)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Spinal muscular atrophy

  2560. CRICKi007-A (iFCI009)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Spinal muscular atrophy with lower extremity predominant

  2561. CRICKi008-A (iFCI006 and NH13-0078)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    X-linked centronuclear myopathy

  2562. CRICKi009-A (iFCI012 and iFCI012 CLONE 4)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Vhl

  2563. CRICKi010-A (iFCI013 and iFCI013 Clone 7)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Vhl

  2564. CRICKi011-A (iFCI016)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Young-onset parkinson disease

  2565. CRICKi012-A (iFCI017)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Young-onset parkinson disease

  2566. CRICKi013-A (iFCI018 Clone 6)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Von hippel-lindau disease tumor suppressor

  2567. CRICKi014-A (iFCI019 Clone 4)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Von hippel-lindau disease tumor suppressor

  2568. CRICKi015-A (iFCI020 Clone 1)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Von hippel-lindau disease tumor suppressor

  2569. CRICKi016-A (iFCI021 Clone 7)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung cancer

  2570. CRICKi017-A (iFCI022 Clone 4)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung cancer

  2571. CRICKi018-A (iKER 12 and iFCI023)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  2572. CRICKi019-A (iKER 8 and iFCI024)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  2573. CRICKi020-A (iFCI025 and iKER 10)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Normal (average)

  2574. CRICKi021-A (iFCI007)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Ullrich congenital muscular dystrophy

  2575. CRICKi022-A (iFCI031)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung cancer

  2576. CRICKi023-A (iFCI032)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Lung squamous cell carcinoma

  2577. CRICKi024-A (XXY-A4)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2578. CRICKi024-B (XXY-2A1)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2579. CRICKi024-C (XXY-3A9)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2580. CRICKi024-D (2A6 C08)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2581. CRICKi024-E (2A6 C11)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2582. CRICKi024-F (2A6 E11)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2583. CRICKi024-G (2A6 H06)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2584. CRICKi024-G-1 (2A6 H06_XO)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2585. CRICKi024-H (3A21)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2586. CRICKi024-H-1 (3A21_XO)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2587. CRICKi024-I (3A43)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2588. CRICKi024-I-1 (3A43_XO)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Klinefelter's syndrome

  2589. CRMi001-A (NCRM-5 and NL-5)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal (average)

  2590. CRMi003-A (NCRM-1 and NL-1)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal (average)

  2591. CRMi004-A (CR0000007, NCRM-2 and ND50030)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal (average)

  2592. CRMi005-A (CR0000011, ND50021 and ND1.4)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal (average)

  2593. CRTDi001-A (T12.9 and C1-1)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2594. CRTDi003-A (CRTD2)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2595. CRTDi003-B (CRTD3)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2596. CRTDi004-A (CRTD1)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2597. CRTDi005-A (CRTD4)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2598. CRTDi005-B (CRTD5)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2599. CRTDi006-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  2600. CRTDi006-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  2601. CRTDi007-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  2602. CRTDi007-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  2603. CRTDi008-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  2604. CRTDi009-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  2605. CRTDi010-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  2606. CRTDi011-A (IDP52555 #9)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2607. CRTDi011-B (IDP52555 #13)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2608. CRTDi011-C (IDP52555 #36)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2609. CRTDi011-D (IDP52555 #44)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  2610. CSBZZUi001-A (CSBZZU_PS1_001)

    China The first affiliated Hospital of Zhengzhou University (CSBZZU)
    Disease:

    Alzheimer disease

  2611. CSBZZUi002-A

    China The first affiliated Hospital of Zhengzhou University (CSBZZU)
    Disease:

    Normal (average)

  2612. CSBZZUi003-A

    China The first affiliated Hospital of Zhengzhou University (CSBZZU)
    Disease:

    Normal (average)

  2613. CSBZZUi004-A

    China The first affiliated Hospital of Zhengzhou University (CSBZZU)
    Disease:

    Normal (average)

  2614. CSCIi001-A (niPSC HDF16 and niPSC-16.2b)

    United Kingdom Wellcome Trust - MRC Stem Cell Institute (CSCI)
    Disease:

    Normal (average)

  2615. CSCIi002-A (niPSC HDF75 and niPSC-75.1c2)

    United Kingdom Wellcome Trust - MRC Stem Cell Institute (CSCI)
    Disease:

    Normal (average)

  2616. CSIRi001-A (CSIR-SA-001-J4)

    South Africa Council for Scientific and Industrial Research South Africa (CSIR)
    Disease:

    Normal (average)

  2617. CSIRi001-B (CSIR-SA-001-J3)

    South Africa Council for Scientific and Industrial Research South Africa (CSIR)
    Disease:

    Normal (average)

  2618. CSIRi002-A (CSIR-SA-001-L2)

    South Africa Council for Scientific and Industrial Research South Africa (CSIR)
    Disease:

    Normal (average)

  2619. CSIRi002-B (CSIR-SA-001-L10)

    South Africa Council for Scientific and Industrial Research South Africa (CSIR)
    Disease:

    Normal (average)

  2620. CSMCi001-A (CS011iMEN1-n4)

    United States Cedars Sinai Medical Center, (CSMC)
    Disease:

    Multiple endocrine neoplasia type 1

  2621. CSMCi001-A-1 (CS011iMEN1-n4.Homo5 and CS011MEN1-n4.HomoMut5)

    United States Cedars Sinai Medical Center, (CSMC)
    Disease:

    Multiple endocrine neoplasia type 1

  2622. CSMCi001-A-2 (2. CS011MEN1-n4.Corrected1)

    United States Cedars Sinai Medical Center, (CSMC)
    Disease:

    Multiple endocrine neoplasia type 1

  2623. CSSi001-A (Joub03cl2 and COR419)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Isolated joubert syndrome

  2624. CSSi002-A (HD8yrs)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Juvenile huntington disease

  2625. CSSi003-A (COL04 clE2)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Smith-magenis syndrome

  2626. CSSi004-A (HD256.05 cl1)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Huntington disease

  2627. CSSi005-A (COL03 cl.C3)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Normal (average)

  2628. CSSi006-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Huntington disease

  2629. CSSi007-A (Joub07 cl1 and COR11-NG708)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Isolated joubert syndrome

  2630. CSSi008-A (AT214-01-02)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Dentatorubral pallidoluysian atrophy

  2631. CSSi009-A (GDB1307_Z2#1)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Gnb5-related intellectual disability-cardiac arrhythmia syndrome

  2632. CSSi011-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Amyotrophic lateral sclerosis

  2633. CSSi012-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Amyotrophic lateral sclerosis

  2634. CSSi013-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Normal (average)

  2635. CSSi014-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Mucopolysaccharidosis ii

  2636. CSSi015-A (FC17)

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Normal (average)

  2637. CSSi016-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Charcot-marie-tooth disease type 4b3

  2638. CSSi017-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Amyotrophic lateral sclerosis

  2639. CSSi018-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    4h leukodystrophy

  2640. CSSi019-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Normal (average)

  2641. CSSi020-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Smith-magenis syndrome

  2642. CSSi021-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Smith-magenis syndrome

  2643. CSSi022-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Charcot-marie-tooth disease type 2a2b

  2644. CSSi023-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Autosomal dominant optic atrophy

  2645. CSUXHi001-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Spinocerebellar ataxia type 3

  2646. CSUXHi002-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Spinocerebellar ataxia type 1

  2647. CSUXHi003-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Waardenburg syndrome type 2

  2648. CSUXHi004-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Waardenburg syndrome type 1

  2649. CSUXHi005-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Spinocerebellar ataxia type 3

  2650. CSUXHEi001-A

    China Central South University (CSUXHE)
    Disease:

    Normal (average)

  2651. CSUXHEi002-A

    China Central South University (CSUXHE)
    Disease:

    Normal (average)

  2652. CTEFi001-A (CTEF-hiPSC10 and FNUSA-hiPSC10)

    Czech Republic Cell and Tissue Engineering Facility (CTEF)
    Disease:

    Normal (average)

  2653. CTGUi001-A (FD01 and F01)

    China China Three Gorges University (CTGU)
    Disease:

    Fabry disease

  2654. CTGUi002-A

    China China Three Gorges University (CTGU)
    Disease:

    Perrault syndrome 5

  2655. CTUi001-A

    China GIBH (CTU)
    Disease:

    Normal (average)

  2656. CTUi005-A (RD001)

    China GIBH (CTU)
    Disease:

    Neurodevelopmental disorder

  2657. CUBi001-A

    Germany Charité - Universitätsmedizin Berlin (CUB)
    Disease:

    Mirage syndrome

  2658. CUBi002-B

    Germany Charité - Universitätsmedizin Berlin (CUB)
    Disease:

    Mirage syndrome

  2659. CUIMCi001-A (ND50003 and FA0000010)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Normal (average)

  2660. CUIMCi002-A (ND50004 and FA0000011)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Normal (average)

  2661. CUIMCi004-A (1514_1)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Class 3 obesity

  2662. CUIMCi004-A-1 (1514_1 #1 CL25)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Class 3 obesity

  2663. CUIMCi004-A-2 (1514_1 #1 CL3)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Class 3 obesity

  2664. CUIMCi004-B

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Class 3 obesity

  2665. CUIMCi005-A (BB#2 and BB9068#2)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Stargardt disease

  2666. CVTTHi001-A

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)
    Disease:

    Activated pi3k-delta syndrome

  2667. CVTTHi001-A-1

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)
    Disease:

    Activated pi3k-delta syndrome

  2668. CVTTHi002-A

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)

  2669. CVTTHi003-A

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)

  2670. CVTTHi004-A

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)

  2671. DANi001-C (iPS-CCD-C3)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Normal (average)

  2672. DANi002-C (GBA-002-C3)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2673. DANi003-H (GBA-003-C8)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2674. DANi004-A (PRKN-004-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2675. DANi005-A (LRRK2-GBA-005-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2676. DANi006-F (GBA-006-C6)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2677. DANi007-A (PINK1-007-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2678. DANi008-F (SNCA-008-C6)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2679. DANi009-C (SNCA-009-C3)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2680. DANi010-A (GBA-010-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2681. DANi011-A (LRRK2-011-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson disease

  2682. DHMi001-A (Control_S)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2683. DHMi002-A (HLHS_606)

    Germany German Heart Center Munich (DHM)
    Disease:

    Hypoplastic left heart syndrome

  2684. DHMi003-A (HLHS_612)

    Germany German Heart Center Munich (DHM)
    Disease:

    Hypoplastic left heart syndrome

  2685. DHMi004-A (HOS_1460)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2686. DHMi004-A-1 (HOS_1460corr 127 Clone 31)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2687. DHMi004-A-2 (HOS_1460_FLAG Clone 4)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2688. DHMi004-A-3 (HOS_1460corr 127 Clone 31_FLAG Clone 18)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2689. DHMi004-A-4 (1460corr_IDT Cl.127_FlagT Clone 7)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2690. DHMi004-A-5 (1460corr_IDT Cl.127_FlagT Clone 25)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2691. DHMi004-A-6 (1460corr_IDT Cl.127_FlagT Clone 26)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2692. DHMi005-A (Control_L)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2693. DHMi005-A-1 (L_mut)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2694. DHMi005-A-2 (L_FLAG Clone 5)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2695. DHMi005-A-3 (L_FLAG Clone 6)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2696. DHMi005-A-4 (L_FLAG Clone 7)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2697. DHMi005-A-5 (L_mut_FLAG Clone 4)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2698. DHMi005-A-6 (L_mut_FLAG Clone 14)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2699. DHMi005-A-7 (L_mut_FLAG Clone 15)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  2700. DHMi005-A-8 (L Delta B2M Clone 6)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2701. DHMi005-A-9 (L Delta B2M Clone 11)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  2702. DHMCi010-A (Neph021C)

    Germany Dietmar Hopp Metabolic Center (DHMC)
    Disease:

    Congenital nephrotic syndrome, finnish type

  2703. DHMCi019-A (Neph018C)

    Germany Dietmar Hopp Metabolic Center (DHMC)
    Disease:

    Familial nephrotic syndrome

  2704. DKFZi001-A (clone 30)

    Germany German Cancer Research Center (DKFZ)
    Disease:

    6q27

    Disease:

    Medulloblastoma

  2705. DKFZi001-B (clone 102)

    Germany German Cancer Research Center (DKFZ)
    Disease:

    6q27

    Disease:

    Medulloblastoma

  2706. DMBi001-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Normal (average)

  2707. DMBi001-A-1

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Laminin alpha 2-related dystrophy

  2708. DMBi001-A-2

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Normal (average)

  2709. DMBi003-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Rheumatoid arthritis

  2710. DMBi004-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Rheumatoid arthritis

  2711. DMBi007-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Psoriasis

  2712. DMBi008-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Psoriasis

  2713. DMBi009-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Becker muscular dystrophy

  2714. DMBi009-A-1

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Becker muscular dystrophy

  2715. DMBi010-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Lymphedema-distichiasis syndrome

  2716. DMSCi001-A

    Thailand Department of Medical Sciences (DMSC)
    Disease:

    Normal (average)

  2717. DMSCi002-A

    Thailand Department of Medical Sciences (DMSC)
    Disease:

    Normal (average)

  2718. DPEDi001-A (T12)

    Germany Division of Paediatric Endocrinology and Diabetes (DPED)
    Disease:

    Normal (average)

  2719. DPNJMUi001-A

    China Children's Hospital of Nanjing Medical University (DPNJMU)
    Disease:

    Combined oxidative phosphorylation deficiency 23

  2720. DPNJMUi002-A

    China Children's Hospital of Nanjing Medical University (DPNJMU)
    Disease:

    Progressive familial intrahepatic cholestasis type 3

  2721. DRICUi002-A (ADANG10242CA)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2722. DRICUi003-A (LC56A10005A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2723. DRICUi004-A (LC56A10012A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2724. DRICUi006-A (ADANG10496CA)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2725. DRICUi007-A (ADANG10605CA)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2726. DRICUi010-A (BS38A10004A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2727. DRICUi011-A (BS38A10002A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2728. DRICUi012-A (NT18A10014A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2729. DRICUi013-A (SC45A10021A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2730. DRICUi014-A (CF00C90323A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2731. DRICUi016-A (GU66A10008a)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2732. DRICUi017-A (FB12A10007a)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2733. DRICUi018-A (BH09A10003A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2734. DRICUi019-A (NE37A10024a)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2735. DRICUi020-A (CF00C90474a)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2736. DRICUi022-A (CF00C90161A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2737. DRICUi023-A (NF35A00021A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2738. DRICUi025-A (CF00C90472A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2739. DRICUi026-A (ADCAR24745UC)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2740. DRICUi027-A (ADCAR20186CA)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2741. DRICUi028-A (NE37A10025A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2742. DRICUi029-A (MW14A10014A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimer's disease

  2743. DRICUi030-A (CF00C90028A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal (average)

  2744. DVSi001-A (KRAS-Q70L-iPSC)

    China Department of Vascular Surgery, The Second Affiliated Hospital of Soochow University (DVS)
    Disease:

    Varicose veins

  2745. EDi001-A (AST22, AST23 and SAMEA3319992)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2746. EDi001-A-1 (AST22-C and AST23-C)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2747. 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

  2748. 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

  2749. 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

  2750. EDi001-A-5 (AST23-2KO-II8B)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2751. EDi001-B (AST18)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2752. EDi001-B-1 (AST18-7A)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2753. EDi001-B-2 (AST18-7B)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2754. EDi001-B-3 (AST18-5D)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2755. EDi001-B-4 (AST18-6A)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2756. EDi002-A (NAS2)

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2757. EDi008-B (G51D-4, EDINi008-B, EDIi008-B and SAMEA3174606)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  2758. EDi010-A (RCi136)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2759. EDi010-B (RCi138)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2760. EDi011-A (RCi139)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2761. EDi011-B (RCi140)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2762. EDi011-C (RCi141)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2763. EDi012-A (RCi163)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2764. EDi012-B (RCi164)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2765. EDi012-C (RCi165)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2766. EDi013-A (RCi192)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2767. EDi013-B (RCi193)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2768. EDi013-C (RCi214)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2769. EDi014-A (RCi175)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Obsolete_unipolar depression

    Disease:

    Anti-social behavior

  2770. EDi014-B (RCi185)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Obsolete_unipolar depression

    Disease:

    Anti-social behavior

  2771. EDi015-A (RCi176)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Obsolete_unipolar depression

  2772. EDi015-B (RCi183)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Obsolete_unipolar depression

  2773. EDi015-C (RCi184)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Obsolete_unipolar depression

  2774. EDi016-A (RCi189)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2775. EDi016-C (RCi191)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2776. EDi017-A (RCi174)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2777. EDi017-B (RCi181)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2778. EDi017-C (RCi182)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2779. EDi018-A (RCi211)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2780. EDi018-B (RCi212)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2781. EDi018-C (RCi213)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  2782. EDi019-A (RCi166)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2783. EDi019-B (RCi167)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2784. EDi019-C (RCi168)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2785. EDi020-A (SFCi55)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2786. EDi021-A (CS0395iCTR-LBCn3)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2787. EDi022-A (CS0617iCTR-LBCn1)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2788. EDi023-A (CS0791iCTR-LBCn1)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2789. EDi024-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2790. EDi025-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2791. EDi026-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2792. EDi027-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2793. EDi028-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2794. EDi029-A

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2795. EDi030-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2796. EDi031-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2797. EDi032-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2798. EDi033-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2799. EDi034-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2800. EDi035-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2801. EDi036-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2802. EDi037-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2803. EDi038-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2804. EDi039-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2805. EDi040-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2806. EDi041-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2807. EDi042-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2808. EDi043-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2809. EDi044-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2810. EDi045-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  2811. EDi046-A

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  2812. EDIi009-A

    China EdiGene. Inc (EDI)
    Disease:

    Duchenne muscular dystrophy

  2813. EHTJUi002-A (DF-GMP-ZB11AR-H)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2814. EHTJUi003-A (DF-GMP-ZB12AD-H)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2815. EHTJUi004-A (DF-GMP-ZB12AN-I)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2816. EHTJUi005-A (DFGMP-ZB11AL-D)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2817. EHTJUi005-A-1 (ZB11ALD-S16-5)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Werner syndrome

  2818. EHTJUi005-A-3 (ZB11ALD-L4)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Hutchinson-gilford progeria syndrome

  2819. EHTJUi006-A (DFGMP-ZB11AN-B)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2820. EHTJUi007-A (DFGMP-ZB11AO-F)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal (average)

  2821. EMCi169-A (Clone 1)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  2822. EMCi169-B (Clone_3)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  2823. EMCi169-C (Clone_9)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  2824. EMCi169-D (Clone_4)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  2825. EMCi169-E (Clone_11)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  2826. EMCi225-A (Clone_2)

    Netherlands Erasmus MC (EMC)
    Disease:

    Neurodevelopmental disorder

  2827. EMCi225-B (Clone_5)

    Netherlands Erasmus MC (EMC)
    Disease:

    Neurodevelopmental disorder

  2828. EMCi225-C (Clone_6)

    Netherlands Erasmus MC (EMC)
    Disease:

    Neurodevelopmental disorder

  2829. EMCi225-D (Clone_8)

    Netherlands Erasmus MC (EMC)
    Disease:

    Neurodevelopmental disorder

  2830. EMCi229-A

    Netherlands Erasmus MC (EMC)
    Disease:

    Normal (average)

  2831. EPFLi001-A (hiPS43)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2832. EPFLi002-A (hiPS9)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2833. EPFLi003-A (hiPS6)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2834. EPFLi004-A (hiPS2)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2835. EPFLi005-A (hiPS45)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2836. EPFLi006-A (hiPS14)

    Switzerland Swiss Federal Institute of Technology (EPFL)
    Disease:

    Normal (average)

  2837. ERPLi004-A (A1AT iPSC C1)

    India Eyestem Research Private Limited (ERPL)
    Disease:

    Alpha 1-antitrypsin deficiency

  2838. ESi001-A (SPO2#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  2839. ESi002-A (SP08#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  2840. ESi003-A ([CRTRd]FiPS3819-4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    X-linked creatine transporter deficiency

  2841. ESi004-A ([GD]FiPS-4F-21c)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Gaucher disease

  2842. ESi005-A (cFA404-KiPS4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Fanconi anemia

  2843. ESi005-B (cFA404-KiPS4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Fanconi anemia

  2844. ESi006-A (SP13#4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  2845. ESi007-A (CBiPS1sv-4F-40)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2846. ESi008-A (KiPS4F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2847. ESi008-B (KiPS3F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2848. ESi028-A (KiPS4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2849. ESi030-A (GA-FiPS4F)

    Spain Spanish Stem Cell Bank (ES)

  2850. ESi031-A (XFiPS-F44-3F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2851. ESi031-B (FiPS-3F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2852. ESi031-C (FiPS-4F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2853. ESi031-D (FiPS-4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2854. ESi032-A (XFiPS-F44-3F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2855. ESi033-A (CBiPS6-2F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2856. ESi034-A (CBiPS30-4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2857. ESi034-B (CBiPS30-4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2858. ESi035-A (AD]FiPSAG07645-4F-17)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_alzheimer's disease

  2859. ESi036-A ([CRTRd]FiPS3067-4F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cerebral creatine deficiency syndrome 1

  2860. ESi037-A (HKiPS-4F)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2861. ESi038-A (CBiPS32-2F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2862. ESi038-B (CBiPS32-3F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2863. ESi038-C (CBiPS32-3F-12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2864. ESi040-A ([PD] FiPS006-4F-11)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_parkinson's disease

  2865. ESi041-A (CBiPS 2F-1c)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2866. ESi041-B (CBiPS 4F-3a)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2867. ESi041-C (CBiPS 4F 10b)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2868. ESi042-A ([TSD] FiPS-4F-3-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Tay-sachs disease

  2869. ESi043-A ([ctrl.PD] FiPS005-4F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2870. ESi044-A (FiPS Ctrl1-mR5F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2871. ESi044-B (FiPS Ctrl1-Ep6F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2872. ESi044-C (FiPS Ctrl1-SV4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2873. ESi044-D (FiPS Ctrl1-R4F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2874. ESi045-A (FiPS Ctrl2-mR5F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2875. ESi045-B (FiPS Ctrl2-Ep6F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2876. ESi045-C (FiPS Ctrl2-SV4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2877. ESi045-D (FiPS Ctrl2-R4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2878. ESi046-A ([UCiPS] Ctrl5-R4F-25)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2879. ESi048-A (MS FiPS 1-R4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

  2880. ESi049-A (MS FiPS 2 R4F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

  2881. ESi050-A (MS FiPS 3-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

  2882. ESi051-A (MS FiPS 4-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

  2883. ESi052-A (MS FiPS 5-R4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

  2884. ESi053-A (MS FiPS 6-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

  2885. ESi054-A (AS FiPS 1-Ep6F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Alport syndrome

  2886. ESi055-A (AS FiPS 2-Ep6F-28)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Alport syndrome

  2887. ESi056-A (AS FiPS 3-Ep6F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Alport syndrome

  2888. ESi057-A ([DUP7] FiPS-4F-3-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2889. ESi057-B ([DUPSW] FiPS301-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2890. ESi058-A ([DUP7] FiPS-4F-4-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2891. ESi058-B ([DUP7] FiPS4-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2892. ESi059-A ([SWB] FiPS-4F-1-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  2893. ESi059-B ([SWB] FiPS1-R4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  2894. ESi060-A ([SWB] FiPS-4F-5-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  2895. ESi060-B ([SWB] FiPS5-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  2896. ESi065-A ([IDDM1] FiPS 1.13-Ep6F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_type i diabetes mellitus

  2897. ESi068-A (SWB FiPS 159-R4F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams-beuren syndrome

  2898. ESi069-A (SWB FiPS 344-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams-beuren syndrome

  2899. ESi070-A (DUPSW FiPS 501-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2900. ESi071-A (DUPSW FiPS 701-R4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  2901. ESi072-A (OCD FiPS 1-EP6F-16)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsessive-compulsive disorder

  2902. ESi073-A (OCD FiPS 2-EP6F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsessive-compulsive disorder

  2903. ESi074-A (CT PBiPS1-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiotoxicity

  2904. ESi075-A (BST PBiPS1-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2905. ESi076-A (BST PBiPS2-Sv4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2906. ESi077-A (CABi001-A and PRPF31-MiPS4F3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Retinitis pigmentosa

  2907. ESi078-A (cPRPF31-MiPS4F7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2908. ESi079-A (cAMDdh09-MiPS4F17)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2909. ESi080-A (N1-FiPS4F#7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2910. ESi081-A (SP11#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2911. ESi082-A (CRB1-MiPS4F1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Macular degeneration

  2912. ESi085-A (cAMDdh01-MiPS4F8 and DH01 c8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2913. ESi086-A (CBiPS8-3F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2914. ESi087-A (BT1-UCiPS4F1 and BT-iPSCs 1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Low grade glioma

  2915. ESi088-A (BT2-UCiPS4F1 and BT-iPSCs 2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Brain cancer

  2916. ESi089-A (Ctrl1-UCiPS4F1 and nonT-iPSCs 1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Inguinal hernia

  2917. ESi090-A (Ctrl2-UCiPS4F1 and nonT-iPSCs 2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cryptorchidism

  2918. ESi091-A (HLA91-MiPS4F3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2919. ESi092-A (HLA98-MiPS4F15)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2920. ESi093-A (CD34 iPS1-Sv4F-B8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2921. ESi094-A (Hz 1-8-3 CBiPS4 Sv4F F6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2922. ESi095-A (Hz 3-7-15 CBiPS3- Sv4F E9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2923. ESi096-A (Hz 11-27-1 CBiPS8-Sv4F-J1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2924. ESi097-A (Hz 24-7-15 CBiPS7 Sv4F-I12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2925. ESi098-A (Hz 30-18-3 CBiPS2-Sv4F-D10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2926. ESi099-A (Hz 33-14-1 CBiPS6-Sv4F H6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2927. ESi100-A (NW FiPS 10II.3-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  2928. ESi101-A (THD FiPS A1 Ep6F-17)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Tyrosine hydroxylase deficiency

  2929. ESi102-A (THD FiPS B1 Ep6F-15)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Tyrosine hydroxylase deficiency

  2930. ESi103-A (OCD FiPS3-Ep6F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsessive-compulsive disorder

  2931. ESi104-A (PMM2-CDG FiPS48-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Pmm2-cdg

  2932. ESi106-A (MD FiPS3304-Sv4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Mitochondrial disease

  2933. ESi107-A (TAC PBiPS1-Sv4F-3 and ATTR-CM PBiPS1-Sv4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  2934. ESi108-A (AFib-C53)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Atrial fibrillation

  2935. ESi110-A (HLA89-MiPS4F8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2936. ESi111-A (Ctrl EiPS J9 mR6F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2937. ESi112-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2938. ESi113-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2939. ESi114-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2940. ESi115-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Inclusion body myositis

  2941. ESi116-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Inclusion body myositis

  2942. ESi117-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Inclusion body myositis

  2943. ESi118-A (MD FiPS3236-Sv4F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Mitochondrial disease

  2944. ESi119-A (SPG FiPS1-Ep6F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Hereditary spastic paraplegia

  2945. ESi120-A (RRMS PBiPS11-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  2946. ESi121-A (RRMS PBiPS12-Sv4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  2947. ESi122-A (PPMS PBiPS7-Sv4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  2948. ESi123-A (PPMS PBiPS8-Sv4F-13)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  2949. ESi124-A (PPMS PBiPS9-Sv4F-12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  2950. ESi128-A (PPMS PBiPS10-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  2951. ESi129-A (RRMS PBiPS13-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  2952. ESi130-A (RRMS PBiPS14-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  2953. ESi132-A (PRPF3181-MiPS4F5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Retinitis pigmentosa

  2954. ESi133-A (CT PBiPS2-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Chemically induced cardiotoxicity

  2955. ESi136-A (NDD PBiPS1-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Neurodevelopmental disorders

  2956. ESi137-A (SSP PBiPS P1-Sv4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Spastic paraparesis

  2957. ESi137-B (SSP PBiPSP1-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Spastic paraparesis

  2958. ESi138-A (ATTR CM PBiPS3-Sv4F-14)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  2959. ESi139-A (ATTR CM PBiPS4-Sv4F-13)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  2960. ESi140-A (CT PBiPS3-Sv4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Chemically induced cardiotoxicity

  2961. ESi141-A (BS PBiPS46-Sv4F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Brugada syndrome

  2962. ESi142-A (ATTR CM PBiPS2-Sv4F-16)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  2963. ESi143-A (Ctrl BS PBiPS37-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  2964. ESi144-A (SPG FiPS2-Ep6F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Hereditary spastic paraplegia

  2965. ESi145-A (LD FiPS18338-Ep6F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Leukodystrophy

  2966. ESi146-A (NEDCASB FiPS319-Ep6F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities

  2967. EUSOMi001-A (3-1 and LQTS003-1)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Long qt syndrome 2

  2968. EUSOMi002-A (LQTS003-3-1 and 3-3-1)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Long qt syndrome 2

  2969. EUSOMi003-A (LQTS003-3-2 and 3-3-2)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Normal (average)

  2970. EUSOMi007-A (2-1 and LQTS002-1)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Long qt syndrome 1

  2971. EXSURGi001-A (SevXC_MTARC1)

    Germany Charité – Universitätsmedizin Berlin (EXSURG)
    Disease:

    Normal (average)

  2972. FAMRCi001-A (ARVC2)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  2973. FAMRCi001-B (ARVC4)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  2974. FAMRCi002-A (OBC7)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Desminopathy

  2975. FAMRCi003-A (108-1)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Normal (average)

  2976. FAMRCi003-B (108-2)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Normal (average)

  2977. 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

  2978. 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

  2979. FAMRCi005-A (LMNA B4)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Paroxysmal ventricular tachycardia

    Disease:

    Atrioventricular block

    Disease:

    Myopathy

  2980. FAMRCi005-B (LMNA B5)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Paroxysmal ventricular tachycardia

    Disease:

    Atrioventricular block

    Disease:

    Myopathy

  2981. FAMRCi006-A (LMNA T3)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  2982. FAMRCi006-B (LMNA T4)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  2983. 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

  2984. 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

  2985. FAMRCi008-A (10X-12)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Normal (average)

  2986. FAMRCi009-A (RCMP43)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Restrictive cardiomyopathy

  2987. FAMRCi010-A (RCMP48)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Restrictive cardiomyopathy

  2988. FAMRCi011-A (ARVC51)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  2989. FAMRCi011-B (ARVC51b)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  2990. FAMRCi012-A (Brug/VT-83)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Ventricular fibrillation

  2991. FAMRCi013-A (ARVC300-14)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  2992. FAMRCi013-B (ARVC300-21)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  2993. FAMRCi013-C (ARVC300-25)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  2994. FAMRCi014-A (177-10)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Hypertrophic cardiomyopathy

  2995. FAMRCi015-A (HCM12f10)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Hypertrophic cardiomyopathy

  2996. FAMRCi015-B (HCM12f23)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Hypertrophic cardiomyopathy

  2997. FCBRNi001-A

    Russia Federal Center of Brain Research and Neurotechnologies (FCBRN)
    Disease:

    Normal (average)

  2998. FCBRNi002-A

    Russia Federal Center of Brain Research and Neurotechnologies (FCBRN)
    Disease:

    Wilson disease

  2999. FDCHi004-A (iPS-39)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Osteogenesis imperfecta

  3000. FDCHi007-A

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Developmental and epileptic encephalopathy 31a

  3001. FDCHi008-A (JYIPS0087)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Chronic intestinal pseudoobstruction

  3002. FDCHi010-A (iPSCx-y-AHDC1-m)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Xia-gibbs syndrome

  3003. FDCHi011-A (iPSC-XX-700-WDR45-m)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  3004. FDCHi012-A (iPSCx-x-DYRK1A-m)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Dyrk1a-related intellectual disability syndrome

  3005. 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

  3006. FDCHi015-A

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Hereditary fructose intolerance

  3007. FDCHi016-A (iPSC-XX-888-WDR45-m)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  3008. FDCHDPi001-A (FDCHDP01)

    China Fudan University (FDCHDP)
    Disease:

    Tourette syndrome

  3009. FDHPIi001-A

    China (WITHDRAWN) Fudan University (FDHPI)
    Disease:

    Neurodegeneration

  3010. FDHSi002-A (FDITBRi002-A)

    China Huashan Hospital of Fudan University (FDHS)
    Disease:

    Parkinson disease

  3011. FDHSi003-A

    China Huashan Hospital of Fudan University (FDHS)
    Disease:

    Gordon holmes syndrome

  3012. FDHSi005-A

    China Huashan Hospital of Fudan University (FDHS)
    Disease:

    Gne myopathy

  3013. 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

  3014. FDZSi002-A

    China Zhongshan Hospital of Fudan University (FDZS)

  3015. FDZSi003-A

    China Zhongshan Hospital of Fudan University (FDZS)
    Disease:

    Prostate cancer

  3016. 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

  3017. 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

  3018. FINi001-A (FI.SPSM.SCN2A.R1882Q.009)

    Australia The Florey Institute of Neuroscience and Mental Health (FIN)
    Disease:

    Developmental and epileptic encephalopathy

  3019. FINi002-A (FI.CPLT.PRKN.R275W+del_e8.PK006)

    Australia The Florey Institute of Neuroscience and Mental Health (FIN)
    Disease:

    Parkinson disease

  3020. FINi006-A (FI.CS.PRKNDex2/Dex5-7.F@40)

    Australia The Florey Institute of Neuroscience and Mental Health (FIN)
    Disease:

    Parkinson disease

  3021. FINi007-A (FI.SP.SLC6A1/GAT1.G307R.032)

    Australia The Florey Institute of Neuroscience and Mental Health (FIN)

  3022. FINi102-A (FI.SP.KCNT1(R950Q/+).NGF026)

    Australia The Florey Institute of Neuroscience and Mental Health (FIN)
    Disease:

    Epilepsy

  3023. FINCBi001-A (F56Lcl33 and F56L 33M)

    Italy Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
    Disease:

    Leber hereditary optic neuropathy

  3024. FINCBi004-A

    Italy Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
    Disease:

    Neurodegeneration with brain iron accumulation 4

  3025. FINCBi005-A (mt1072 clone #103 and mt1072 #103)

    Italy Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
    Disease:

    Leber hereditary optic neuropathy

  3026. FINCBi006-A (mt1108 clone #121 and mt1108 #121)

    Italy Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
    Disease:

    Leber hereditary optic neuropathy

  3027. FJMAi001-A

    China Fujian Academy of Medical Sciences (FJMA)
    Disease:

    Marfan syndrome

  3028. FJMUi001-A (hiPS-SPG76-001)

    China Fujian Medical University (FJMU)
    Disease:

    Hereditary spastic paraplegia

  3029. FJMUNi001-A

    China Department of Neurology, Fujian Institute of Neurology, the First Affiliated Hospital, Fujian Medical University (FJMUN)
    Disease:

    Duchenne muscular dystrophy

  3030. FJMUUHi001-A

    China Fujian Medical University Union Hospital (FJMUUH)
    Disease:

    Parkinson's disease 7

  3031. FJMUUHi002-A

    China Fujian Medical University Union Hospital (FJMUUH)
    Disease:

    Rett syndrome

  3032. FLENIi004-A (FBAD1)

    Argentina Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia (FLENI)
    Disease:

    Familial alzheimer disease

  3033. FMCPGHi001-A (301-iPSC-normal-001A)

    China The First Medical Center of PLA General Hospital (FMCPGH)
    Disease:

    Normal (average)

  3034. FMCPGHi002-A (301-iPSC-normal-002B)

    China The First Medical Center of PLA General Hospital (FMCPGH)
    Disease:

    Normal (average)

  3035. FMCPGHi003-A (301-iPSC-FHM-001A)

    China The First Medical Center of PLA General Hospital (FMCPGH)
    Disease:

    Familial hemiplegic migraine 3

  3036. FMCPGHi006-A

    China The First Medical Center of PLA General Hospital (FMCPGH)
    Disease:

    Duchenne muscular dystrophy

  3037. FMMUNIi001-A (I-WT)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Normal (average)

  3038. FMMUNIi002-A (I-IF)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Ventricular fibrillation

  3039. FMMUNIi003-A (I-CPVT)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3040. 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:

    Mental retardation

  3041. FPHYBi001-A (CYY250222)

    China First People’s Hospital of Yibin (FPHYB)
    Disease:

    Normal (average)

  3042. FRIMOi001-A (RP1_FiPS4F1.6)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Retinitis pigmentosa

  3043. FRIMOi002-A (RP2_FiPS4F2.2)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Retinitis pigmentosa

  3044. FRIMOi003-A (STGD1_ FiPS4F1.5)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Stargardt disease

  3045. FRIMOi004-A (STGD2_ FiPS4F1.7)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Stargardt disease

  3046. FRIMOi005-A (RP3_FiPS4F11)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Retinitis pigmentosa

  3047. FRIMOi006-A (BEST1_FiPS4F1)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Bestrophinopathy

  3048. FRIMOi007-A (PDE6C_FiPS4F1)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Achromatopsia

  3049. FSMi001-A (FSM-SPG31-2)

    Italy IRCCS Fondazione Stella Maris (FSM)
    Disease:

    Spastic paraplegia 31

  3050. FUHSi001-A

    China Huashan Hospital of Fudan University (FUHS)
    Disease:

    Cervical artery dissection

  3051. GEMi001-A (GN-IPS-12-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3052. GEMi002-A (GN-IPS-14-2)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3053. GEMi003-A (GN-IPS-15-2)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3054. GEMi004-A (GN-IPS-135-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3055. GEMi005-A (GN-IPS-160-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3056. GEMi006-A (GN-IPS-201-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3057. GEMi007-A (GN-IPS-202-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3058. GEMi008-A (GN-IPS-203-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3059. GEMi009-A (GN-IPS-204-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3060. GEMi010-A (GN-IPS-205-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3061. GEMi011-A (GN-IPS-206-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3062. GEMi011-A-1 (GN-JY02-02-011(PSEN1-exon9-KO))

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Alzheimer disease

  3063. GEMi012-A (GN-IPS-207-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3064. GEMi013-A (GN-IPS-208-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3065. GEMi014-A (GN-IPS-209-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3066. GEMi015-A (GN-IPS-210-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3067. GEMi016-A (GN-IPS-211-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3068. GEMi017-A (GN-IPS-212-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3069. GEMi018-A (GN-IPS-213-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3070. GEMi019-A (GN-IPS-214-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3071. GEMi020-A (GN-IPS-215-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3072. GEMi021-A (GN-IPS-216-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3073. GEMi022-A (GN-IPS-217-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3074. GEMi022-A-1 (GN-JY02-01-001(APP c.2010-2011 inv))

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Alzheimer disease

  3075. GEMi022-A-2 (GN-JY02-01-008(PSEN1 c.313T>C))

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Alzheimer disease

  3076. GEMi022-A-3 (GN-JY02-01-012(APP c.2149G>A))

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Alzheimer disease type 1

  3077. GEMi023-A (GN-IPS-218-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3078. GEMi024-A (GN-IPS-219-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3079. GEMi025-A (GN-IPS-220-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3080. GEMi026-A (GN-IPS-46-3)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  3081. GENYOi001-A (PBMC1-iPS4F1)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal (average)

  3082. GENYOi003-A (PBMC2-iPS4F8)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal (average)

  3083. GENYOi004-A (ASD-PBMC-iPS4F2)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Adnp syndrome

  3084. GENYOi005-A (FPD/AML-PBMC-iPSC4F73)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Familial platelet disorder with associated myeloid malignancy

  3085. GENYOi006-A (GRX-MCiPS4F-A2)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal (average)

  3086. GENYOi006-A-1 (GRX-MCiPS4F-A2-ETO2-GLIS2)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Acute myeloid leukemia

  3087. GENYOi006-A-2 (GRX-MCiPS4F-A2-NEO)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal (average)

  3088. GENYOi007-A (W8)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Meniere disease

  3089. GIBHi001-A

    China Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences (GIBH)
    Disease:

    Autism spectrum disorder

  3090. GIBHi002-A (C11)

    China Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences (GIBH)
    Disease:

    Normal (average)

  3091. GIBHi002-A-1 (C5-PARK2-KO)

    China Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences (GIBH)
    Disease:

    Parkinson disease

  3092. GIBHi003-A (PINK1-I368N-C2)

    China Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences (GIBH)
    Disease:

    Parkinson disease

  3093. GLNNFi001-A

    India GROW Laboratory (GLNNF)
    Disease:

    Macular corneal dystrophy

  3094. GRi001-A (572)

    France Gustave Roussy (GR)
    Disease:

    Normal (average)

  3095. GRi002-A (534)

    France Gustave Roussy (GR)
    Disease:

    Normal (average)

  3096. GRi003-A

    France Gustave Roussy (GR)
    Disease:

    Normal (average)

  3097. GRCHJUi001-A (LYJ-iPS-C)

    China Guangzhou Red Cross Hospital of Jinan University (GRCHJU)
    Disease:

    Atrial fibrillation

  3098. GWCMCi001-A (iPS-57)

    China Guangzhou Women and Children's Medical Center (GWCMC)
    Disease:

    Iga glomerulonephritis

  3099. GWCMCi005-A (GWCMCi-TANC2)

    China Guangzhou Women and Children's Medical Center (GWCMC)
    Disease:

    Lennox-gastaut syndrome

  3100. GWCMCi006-A (GWCMCi-GRIN1)

    China Guangzhou Women and Children's Medical Center (GWCMC)
    Disease:

    Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant

  3101. GZHMCi011-A (SCA3-LXM)

    China The Third Affiliated Hospital of Guangzhou Medical University (GZHMC)
    Disease:

    Normal (average)

  3102. HCORDi001-A (M2_IPSC3_A)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3103. HCORDi001-B (M2_IPSC3_B)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3104. HCORDi001-C (M2_IPSC3_C)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3105. HCORDi001-D (M2_IPSC3_K)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3106. HCORDi001-E (M2_IPSC3_L)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3107. HCORDi001-F (M2_IPSC3_M)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3108. HCORDi001-G (M2_IPSC3_N)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3109. HCORDi001-H (M2_IPSC3_O)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3110. HCORDi001-I (M2_IPSC4_P)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3111. HCORDi001-J (M2_IPSC4_R)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  3112. HDZi001-A (hiPSC NP0039)

    Germany Heart and Diabetes Center North Rhine Westphalia (HDZ)
    Disease:

    Arrhythmogenic right ventricular dysplasia 5

  3113. HDZi003-A (hiPSC NP0038)

    Germany Heart and Diabetes Center North Rhine Westphalia (HDZ)
    Disease:

    Arrhythmogenic right ventricular dysplasia 5

  3114. HDZi003-A-1

    Germany Heart and Diabetes Center North Rhine Westphalia (HDZ)
    Disease:

    Arrhythmogenic right ventricular dysplasia 5

  3115. HEBHMUi001-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Parkinson disease

  3116. HEBHMUi002-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3117. HEBHMUi003-A (HCHB-003)

    China Hebei Medical University (HEBHMU)
    Disease:

    Amyotrophic lateral sclerosis

  3118. HEBHMUi004-A (ALSHB-004)

    China Hebei Medical University (HEBHMU)
    Disease:

    Amyotrophic lateral sclerosis

  3119. HEBHMUi005-A (HCHB-005)

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3120. HEBHMUi007-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3121. HEBHMUi008-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Cerebrovascular disease

  3122. HEBHMUi009-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Obsolete_alzheimer's disease

  3123. HEBHMUi010-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3124. HEBHMUi011-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Obsolete_alzheimer's disease

  3125. HEBHMUi012-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Hypertension

  3126. HEBHMUi013-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Alzheimer's disease

  3127. HEBHMUi014-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Alzheimer disease

  3128. HEBHMUi015-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3129. HEBHMUi017-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  3130. HEBHMUi018-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Baraitser-winter syndrome 1

  3131. HELPi001-A (BS-TL-1)

    China Help Stem Cell Innovations Co.Ltd. (HELP)
    Disease:

    Congenital contractural arachnodactyly

  3132. HHUi003-B (A4_C1)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Maternally-inherited leigh syndrome

  3133. HHUi003-C (A4_W1)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Maternally-inherited leigh syndrome

  3134. HHUi006-A (11656_H)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Normal (average)

  3135. HHUi006-B (11656_K)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Normal (average)

  3136. HHUUKDi001-A (ISRM-UM51 and UM51-iPSC)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Normal (average)

  3137. HHUUKDi009-A (TFBJ)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Normal (average)

  3138. HHUUKDi011-A (AATD iPSC-1 and ISRM-AATD-iPSC-1)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Alpha-1 antitrypsin deficiency

  3139. HHUUKDi012-A (AATD iPSC-2 and ISRM-AATD-iPSC-2)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Alpha-1 antitrypsin deficiency

  3140. HHUUKDi013-A (ISRM-AATD-iPSC-3)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Alpha-1 antitrypsin deficiency

  3141. HHUUKDi014-A (ISRM-BS3-iPSC)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)

  3142. HIHCNi008-A (iPSC-CO-4)

    Germany Hertie Institute for Clinical Brain Research - Clinical Neurogenetics (HIHCN)
    Disease:

    Normal (average)

  3143. HIHCNi008-A-3 (iPSC-REEP1_homKO2)

    Germany Hertie Institute for Clinical Brain Research - Clinical Neurogenetics (HIHCN)
    Disease:

    Hereditary spastic paraplegia 31

  3144. HIHCNi008-A-4 (iPSC-REEP1_hetKO2)

    Germany Hertie Institute for Clinical Brain Research - Clinical Neurogenetics (HIHCN)
    Disease:

    Hereditary spastic paraplegia 31

  3145. HIHCNi008-A-5 (iPSC-M1SPAST_homKO2)

    Germany Hertie Institute for Clinical Brain Research - Clinical Neurogenetics (HIHCN)
    Disease:

    Autosomal dominant spastic paraplegia type 4

  3146. HIHCNi008-A-6 (iPSC-M1SPAST_hetKO2)

    Germany Hertie Institute for Clinical Brain Research - Clinical Neurogenetics (HIHCN)
    Disease:

    Autosomal dominant spastic paraplegia type 4

  3147. 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

  3148. 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

  3149. HIHRSi004-A

    Germany Hertie Institute for Clinical Brain Research, AG Schüle (HIHRS)
    Disease:

    Spastic ataxia

  3150. HIHRSi005-A

    Germany Hertie Institute for Clinical Brain Research, AG Schüle (HIHRS)
    Disease:

    Spastic ataxia

  3151. HIHRSi006-A

    Germany Hertie Institute for Clinical Brain Research, AG Schüle (HIHRS)
    Disease:

    Spastic ataxia

  3152. HIMRi001-A (p.Q1662X FLNC hiPSCs)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Muscle filaminopathy

  3153. HIMRi002-A (p.A46T CAV3 hiPSCs #1)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Caveolinopathy

  3154. HIMRi003-A (p.A46T CAV3 hiPSCs #2)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Caveolinopathy

  3155. HIMRi004-A (FLNC p.W2710X hiPSC)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Muscle filaminopathy

  3156. HIMRi005-A (FLNC p.Y2704X hiPSC)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Muscle filaminopathy

  3157. 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

  3158. 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

  3159. HKUi002-A (AYC12 and HKUi002-A-AYC12)

    Hong Kong The University of Hong Kong (HKU)
    Disease:

    Dilated cardiomyopathy

  3160. HMGUi001-A (XM001 and BIHi043-A)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Normal (average)

  3161. HMGUi001-A-1 (hINS-T2A-H2B-Cherry (+/-) and HMGUi001-A-1)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Normal (average)

  3162. HMGUi002-A (XM002)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Normal (average)

  3163. HMGUi003-A

    Germany Helmholtz Zentrum München (HMGU)

  3164. HMGUi004-A

    Germany Helmholtz Zentrum München (HMGU)

  3165. HMGUi005-A (150553)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  3166. HMGUi006-A (152350)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  3167. HMSi001-A (GM27938)

    United States Harvard Medical School (HMS)
    Disease:

    Kif1a related neurological disorder

  3168. HMSi001-B (GM27937)

    United States Harvard Medical School (HMS)
    Disease:

    Kif1a related neurological disorder

  3169. HMSi002-A (GM27934)

    United States Harvard Medical School (HMS)
    Disease:

    Kif1a related neurological disorder

  3170. HMSCATi001-A

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Normal (average)

  3171. HMSCATi002-A

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Normal (average)

  3172. HMSCATi003-A (PJW)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Parkinson disease

  3173. HMSCATi004-A (LHK)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Young-onset parkinson disease

  3174. HMSCATi005-A (LQH)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Alzheimer's disease

  3175. HMSCATi006-A (CYJ-C1)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Epileptic encephalopathy

  3176. HMSCATi007-A (GXM)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Epilepsy, familial focal, with variable foci 1

  3177. HMSCATi008-A (TSC1-PL)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Tuberous sclerosis

    Disease:

    Epilepsy

  3178. HMSCATi009-A (WZX)

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Frontotemporal dementia

  3179. HMUCPi001-A

    China Harbin Medical University College of Pharmacy (HMUCP)
    Disease:

    Hypertrophic cardiomyopathy

  3180. HNMUi002-A (iPS-UC1291)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  3181. HNMUi003-A (iPS-UC1290)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  3182. HNMUi004-A (iPS-AF717)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  3183. HNMUi005-A (iPS-UC1056)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  3184. HNMUi006-A (iPS-UC1055)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  3185. HNMUi007-A (iPS-AF0442)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  3186. HNMUi008-A (iPS-UC2419)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  3187. HNMUi009-A (iPS-UC1171)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  3188. HNMUi010-A (iPS-AF091)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  3189. HPCHi001-A

    China Henan Provincial Chest Hospital (HPCH)
    Disease:

    Familial hypercholesterolemia

  3190. HPCHi002-A

    China Henan Provincial Chest Hospital (HPCH)
    Disease:

    Dilated cardiomyopathy

  3191. HPIi005-A (RYR1-5-9214-iPSC clone R5)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  3192. HPIi005-B (RYR1-5-9214-iPSC clone R11)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  3193. HPIi006-A (RYR1-3278-R2A)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  3194. HPIi008-A (RYR1-4833-R7)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  3195. HPIi009-A (RYR1-15377-R1B)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  3196. HPIi010-A (MYH7-17773-R4A)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Myh7-related skeletal myopathy

  3197. HPIi011-A (MYH7-18681-R1A)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Myh7-related skeletal myopathy

  3198. HPIi012-A (MYH7-19203-R1D)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Myh7-related skeletal myopathy

  3199. HPIi013-A (OPDM_ABCD3)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Oculopharyngodistal myopathy

  3200. HUBi001-A (HUB001Ai)

    Netherlands The Hubrecht Institute (HUB)
    Disease:

    Normal (average)

  3201. HUJIi001-A (iWSM-F1)

    Israel Hebrew University of Jerusalem (HUJI)
    Disease:

    Developmental and epileptic encephalopathy, 28

  3202. HUJIi002-A (iWSM-M2)

    Israel Hebrew University of Jerusalem (HUJI)
    Disease:

    Developmental and epileptic encephalopathy, 28

  3203. HUJIi003-A (iWSM-S5)

    Israel Hebrew University of Jerusalem (HUJI)
    Disease:

    Developmental and epileptic encephalopathy, 28

  3204. HUJIi004-A (ITM-iPS10)

    Israel Hebrew University of Jerusalem (HUJI)

  3205. HUJIi004-B (ITM-iPS11)

    Israel Hebrew University of Jerusalem (HUJI)

  3206. HUJIi005-A (ID-iPS7)

    Israel Hebrew University of Jerusalem (HUJI)

  3207. HUJIi005-B (ID-iPS10)

    Israel Hebrew University of Jerusalem (HUJI)

  3208. HUSTTJi001-A

    China Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology (HUSTTJ)
    Disease:

    Moyamoya disease

  3209. HVRDi004-B (GM23338)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  3210. HVRDi004-B-1 (ENCBS369AAA and iNGN)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  3211. HVRDi005-A (BJ SiPS-D)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  3212. HVRDi006-A (18b healthy control)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  3213. HVRDi007-A (DiPS 1016SevA)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  3214. HVRDi008-A (SOD1-27e and 27e)

    United States Harvard University (HVRD)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  3215. HVRDi009-A (29e SOD1 L144F and 29e)

    United States Harvard University (HVRD)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  3216. HVRDi010-A (19a)

    United States Harvard University (HVRD)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  3217. HZSMHCi001-A

    China Hangzhou Seventh People’s Hospital Mental Health Center, Zhejiang University School of Medicine (HZSMHC)
    Disease:

    Bipolar disorder

  3218. HZSMHCi002-A

    China Hangzhou Seventh People’s Hospital Mental Health Center, Zhejiang University School of Medicine (HZSMHC)
    Disease:

    Neuronal intranuclear inclusion disease

  3219. HZSMHCi003-A

    China Hangzhou Seventh People’s Hospital Mental Health Center, Zhejiang University School of Medicine (HZSMHC)
    Disease:

    Fragile x syndrome

  3220. HZSMHCi004-A

    China Hangzhou Seventh People’s Hospital Mental Health Center, Zhejiang University School of Medicine (HZSMHC)
    Disease:

    Major depressive disorder

  3221. IAIi001-A (IAIi001RSTS2-65-A)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  3222. IAIi002-A (IAIi002RSTS1-34-A)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  3223. IAIi003-A (IAIi003RSTS1-46-A)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  3224. IAIi004-A (IAIi004RSTS1-149-A)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  3225. IAIi005-A (AC52)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Normal (average)

  3226. IAIi006-A (BC6)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Amyotrophic lateral sclerosis

  3227. IAIi007-A (CC5)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Amyotrophic lateral sclerosis

  3228. IAIi008-A (DC2)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Amyotrophic lateral sclerosis

  3229. IAIi009-A (EC1)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Normal (average)

  3230. IAIi010-A (Kif5A 1847 C3)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Autosomal dominant spastic paraplegia type 10

  3231. IBBISTi004-A (AS-GB clone 12)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  3232. IBBISTi004-B (AS-GB clone 20)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  3233. IBBISTi004-C (AS-GB clone 22)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  3234. IBBISTi005-A (F81 (940) clone 5)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3235. IBBISTi005-B (F81 (940) clone 8)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3236. IBBISTi006-A (F93 clone 5)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3237. IBBISTi006-B (F93 clone 6)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3238. IBBISTi007-A (6F26)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3239. IBBISTi007-B (2F26)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3240. IBBISTi008-A (8F82)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3241. IBBISTi008-B (3F82)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3242. IBBISTi009-A (1F97)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3243. IBBISTi009-B (5F97)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3244. IBBISTi010-A (4_H17)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3245. IBBISTi011-A (3_H24)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3246. IBBISTi012-A (6_H35)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3247. IBBISTi013-A (4_H22)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  3248. IBBISTi014-A (Ctrl-MD1 (clone O))

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Normal (average)

  3249. IBBISTi015-A (AS-MD1 (clone N))

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  3250. IBBISTi016-A (Ctrl-MD2 (clone 7))

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Normal (average)

  3251. IBBISTi017-A (AS-MD2 (clone Q))

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  3252. IBKMOLi002-A (CACNA1D L271H iPCs)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Autism spectrum disorder

    Disease:

    Hyperinsulinemic hypoglycemia

    Disease:

    Primary hyperaldosteronism

    Disease:

    Muscle hypotonia

  3253. IBKMOLi003-A (vEDS COL3A1 Q105* iPSC)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Vascular ehlers-danlos syndrome

  3254. IBKMOLi004-A (sCeAD iPSC)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)

  3255. IBKMOLi005-A (CTRL iPSC)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Normal (average)

  3256. IBKMOLi006-A (GM08399 iPSCs)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Normal (average)

  3257. IBKMOLi007-A (GM03440 iPSCs)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Normal (average)

  3258. IBMSi001-A (IBMS-iPSC-012-12)

    Taiwan Institute of Biomedical Sciences, Academia Sinica (IBMS)
    Disease:

    Autosomal dominant polycystic kidney disease

  3259. IBMSi002-A (IBMS-iPSC-013-06)

    Taiwan Institute of Biomedical Sciences, Academia Sinica (IBMS)
    Disease:

    Autosomal dominant polycystic kidney disease

  3260. IBMSi003-A (IBMS-iPSC-014-05)

    Taiwan Institute of Biomedical Sciences, Academia Sinica (IBMS)
    Disease:

    Autosomal dominant polycystic kidney disease

  3261. IBMSi027-A (IBMS-iPSC-073-01)

    Taiwan Institute of Biomedical Sciences, Academia Sinica (IBMS)
    Disease:

    Wolfram syndrome

  3262. BIONi010-C-65 (BiONI010-C-O16)

    Germany Fraunhofer Institute for Biomedical Engineering IBMT (IBMT)
    Disease:

    Cystic fibrosis

  3263. BIONi010-C-66 (BIONi010-C-N7)

    Germany Fraunhofer Institute for Biomedical Engineering IBMT (IBMT)
    Disease:

    Cystic fibrosis

  3264. IBPi001-A (HPrF iPSCs 20A)

    Czech Republic Institute of Biophysics of the Czech Academy of Sciences (IBP)
    Disease:

    Normal (average)

  3265. IBPi002-A (P71 iPSCs 1)

    Czech Republic Institute of Biophysics of the Czech Academy of Sciences (IBP)
    Disease:

    Prostate adenocarcinoma

  3266. IBTCMi001-A (NDC1)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Normal (average)

  3267. IBTCMi002-A (NDC2)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Normal (average)

  3268. IBTCMi003-A (AD1)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Alzheimer's disease

  3269. IBTCMi004-A (AD2)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Alzheimer's disease

  3270. IBTCMi005-A (AD3)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Alzheimer's disease

  3271. IBTCMi006-A (ACNE1)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Acne

  3272. IBTCMi007-A (ACNE2)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Acne

  3273. ICANi001-A (CDGEN1.16)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Hypertrophic cardiomyopathy

  3274. ICANi001-A-1 (CDGEN1.16.40.5)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Hypertrophic cardiomyopathy

  3275. ICANi002-A (ICAN-403.3)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal (average)

  3276. ICANi002-A-1 (ICAN-FLNC42.1)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal (average)

  3277. ICANi002-A-2 (SCN5A-Clone 5)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal (average)

  3278. ICANi002-A-3 (ICAN-BAG3-V468MC34)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Dilated cardiomyopathy 1hh

  3279. ICANi002-A-4 (ICAN_BAG3_M468MC19)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Dilated cardiomyopathy 1hh

  3280. ICANi002-A-5 (ICAN-PKP2-H695-W11)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Arrhythmogenic right ventricular dysplasia 9

  3281. ICANi002-A-6 (ICAN-ENTREP1-KO-5.3.14)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal (average)

  3282. ICGi002-A (DMD1_1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  3283. ICGi002-B (DMD1_4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  3284. ICGi002-C (DMD1_11)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  3285. ICGi003-A (f3SMA3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Spinal muscular atrophy type 3

  3286. ICGi005-A (iSMA40)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 1

  3287. ICGi005-B (iSMA37)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 1

  3288. ICGi006-A (m3SMA13)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 2

  3289. ICGi006-B (m3SMA20)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 2

  3290. ICGi007-A (47Q-3Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  3291. ICGi008-A (m55Alz-9L)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_alzheimer's disease

  3292. ICGi008-B (m55Alz-15L)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_alzheimer's disease

  3293. ICGi009-A (iTAF3-17 and iTAF3del17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  3294. ICGi009-B (iTAF3del37 and iTAF3-37)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  3295. ICGi013-A (iTAF13-26 and iTAF13del26)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  3296. ICGi013-B (iTAF13del27 and iTAF13-27)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  3297. ICGi014-A (2M_iALS)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  3298. ICGi015-A

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3299. ICGi015-B

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3300. ICGi015-B-1 (m6.7pCyto-17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3301. ICGi015-B-2 (m6.7pCyto-21)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3302. ICGi015-B-3 (m6.7pCyto-24)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3303. ICGi016-A (iTaf9-11)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Mental retardation, autosomal dominant 39

  3304. ICGi017-A (TAF14dup10)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3305. ICGi018-A (iHD38Q-3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  3306. ICGi018-B (iHD38Q-2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  3307. ICGi018-C (iHD38Q-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  3308. ICGi019-A (HCM1f6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3309. ICGi019-B (HCM1f33)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3310. ICGi019-B-1 (HCM1f33-wt119)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3311. ICGi019-B-2 (HCM1f33-wt147)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3312. ICGi020-A (ATP7bIL23f)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Wilson disease

  3313. ICGi020-B (ATP7bIL24f)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Wilson disease

  3314. ICGi021-A (K6-4f)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3315. ICGi021-A-1 (K6-4fpCyto-13)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy

  3316. ICGi021-A-2 (K6-4fpCyto-16)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy

  3317. ICGi021-A-3 (K6-4fpCyto-19)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy

  3318. ICGi022-A (K7-4Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3319. 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

  3320. 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

  3321. ICGi022-A-3 (K7-MYBPC3-N515del-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3322. ICGi022-A-4 (K7-MYBPC3-N515del-2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3323. ICGi022-A-5 (K7-MYBPC3-N515del-3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3324. ICGi022-A-6 (K74-AsCas12a-N1-26)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3325. ICGi022-A-7 (K74-AsCas12aY1-17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3326. ICGi022-A-8 (K7-4 T32)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3327. ICGi022-A-9 (K7-4Lf MT21)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3328. ICGi022-A-10 (K7-4Lf MT16)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3329. ICGi022-B (K7-2Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy subject

  3330. ICGi023-A (PD45-6-1Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3331. ICGi024-A

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Ring chromosome 18 syndrome

  3332. ICGi025-A (iTAF11-4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Developmental delay

  3333. ICGi026-A

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Fragile x syndrome

  3334. ICGi028-A (HCM4fm5.2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3335. ICGi029-A (HCM14fm6.2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3336. ICGi029-A-1 (HCM14-3wt1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3337. ICGi029-A-2 (HCM14-3wt8)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3338. ICGi029-A-3 (HCM14-3wt31)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3339. ICGi030-A (HF2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Wilson disease

  3340. ICGi032-A

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Fragile x syndrome

  3341. ICGi033-A (77Q-17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  3342. ICGi033-B (77Q-9)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  3343. ICGi033-C (77Q-20)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  3344. ICGi034-A (PD30-4-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3345. 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

  3346. 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

  3347. 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

  3348. 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

  3349. ICGi034-B (PD30-5-16)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3350. ICGi034-C (PD30-5-27)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3351. ICGi034-D (PD30-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3352. ICGi034-E (PD30-3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  3353. ICGi035-A (iCS-MAF1-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3354. ICGi035-B (iCS-MAF1-11)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3355. ICGi036-A (FH 1.3.1S)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hyperlipoproteinemia, type iia

  3356. 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

  3357. ICGi037-A (FH 3.2.8T)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hyperlipoproteinemia, type iia

  3358. ICGi038-A (FH 5.1.2Sh)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hyperlipoproteinemia, type iia

  3359. ICGi039-A (PD31-6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3360. ICGi039-B (PD31-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3361. ICGi039-C (PD31-15)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3362. ICGi040-A (iTAF16-3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Infertility

  3363. ICGi042-A (PD12-4Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3364. ICGi042-B (PD12-5Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3365. ICGi042-C (PD12-6Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3366. ICGi043-A (LR-21)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3367. ICGi043-A-1 (LR-21-cytoGRX-3c)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3368. ICGi043-B (LR-2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3369. ICGi043-C (LR-15)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3370. ICGi044-A (PD40-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3371. ICGi044-B (PD40-8)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3372. ICGi044-C (PD40-13)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3373. ICGi045-A (M-5)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Rasopathy

  3374. ICGi046-A (V2-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Rasopathy

  3375. ICGi047-A (ГК10-31 and HC10-31)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  3376. ICGi052-A (PD57-6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Frontotemporal dementia

  3377. ICGi052-B (PD57-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Frontotemporal dementia

  3378. ICGi052-B-1 (PD57-7 MT8)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Frontotemporal dementia

  3379. ICGi052-B-2 (PD57-7 MT6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Frontotemporal dementia

  3380. ICGi053-A (PD58-4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3381. ICGi053-B (PD58-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3382. ICGi053-C (PD58-14)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3383. ICGi054-A (PD69-1/1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3384. ICGi054-B (PD69-2/1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3385. ICGi054-C (PD69-4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3386. ICGi054-D (PD69-5)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3387. ICGi057-A (K9-4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal (average)

  3388. ICGi058-A (iP63)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Autism spectrum disorder

  3389. ICGi059-A (iHD46Q7.1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  3390. ICGi060-A (PD92-22)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3391. ICGi060-B (PD92-21)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3392. ICGi060-C (PD92-39)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson disease

  3393. ICHi001-A (TTNtv-001)

    Italy IRCCS Istituto Clinico Humanitas (ICH)
    Disease:

    Cardiomyopathy, dilated

  3394. ICHi002-A (TTNtv-002)

    Italy IRCCS Istituto Clinico Humanitas (ICH)
    Disease:

    Cardiomyopathy, dilated

  3395. ICHi003-A (TTNtv-003)

    Italy IRCCS Istituto Clinico Humanitas (ICH)
    Disease:

    Cardiomyopathy, dilated

  3396. ICHi004-A (TTNtv-004)

    Italy IRCCS Istituto Clinico Humanitas (ICH)
    Disease:

    Cardiomyopathy, dilated

  3397. ICNDXHi001-A

    China Innovation Center for Neurological Disorders, Xuanwu Hospital, National Clinical Research Center for Geriatric Diseases (ICNDXH)
    Disease:

    Frontotemporal dementia

  3398. ICSSUi002-A

    China Institute for Cardiovascular Science of Soochow University (ICSSU)
    Disease:

    Aortic dissection

  3399. ICSSUi004-A

    China Institute for Cardiovascular Science of Soochow University (ICSSU)
    Disease:

    Restrictive cardiomyopathy

  3400. ICSSUi005-A

    China Institute for Cardiovascular Science of Soochow University (ICSSU)
    Disease:

    Maternally-inherited diabetes and deafness

  3401. ICSSUi006-A

    China Institute for Cardiovascular Science of Soochow University (ICSSU)
    Disease:

    Dilated cardiomyopathy

  3402. IDIBGIi001-A (GPG1-C23)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Normal (average)

  3403. IDIBGIi002-A (RB20234)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Brugada syndrome

  3404. IDIBGIi003-A (​RB20235)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Brugada syndrome

  3405. IDIBGIi004-A (RB20236)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Brugada syndrome

  3406. IDIBGIi005-A (RB20237)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Normal (average)

  3407. 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

  3408. 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

  3409. 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

  3410. 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

  3411. IDIBGIi010-A (RB20655 and ​CPVT FiPS 55 EP6F-8)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Normal (average)

  3412. IDISi001-A

    Spain Health Research Institute of Santiago de Compostela (IDIS)
    Disease:

    Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy

  3413. IDMi001-A (K40)

    Germany Institute for Diabetes Research and Metabolic Diseases (IDM)
    Disease:

    Prediabetes syndrome

  3414. HMGUi001-A-4 (hiPSC-ARX-T2A-H2B-CFP-Flag)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3415. HMGUi001-A-5 (ΔINK4 T2D risk region hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3416. HMGUi001-A-8 (C-PEP-mCherry-hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3417. HMGUi001-A-42 (NEUROD2 nVenus/nVenus iPSCs)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3418. 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)

  3419. 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)

  3420. 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)

  3421. HMGUi001-A-55 (Flattop-T2A-H2B-Venus-hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3422. HMGUi001-A-56 (Flattop-T2A-H2B-VenusxC-Peptide-mCherry-hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3423. HMGUi001-A-61 (SYT13-KOnVenus/nVenus-hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal (average)

  3424. IDVi001-A (iPS-NR2E3-86)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinitis pigmentosa

  3425. IDVi002-A (iPS-PRPF31-4138)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Normal (average)

  3426. IDVi005-A (hiPSC_5f)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Normal (average)

  3427. IDVi006-A (UBAP1L-3225)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinal dystrophy

  3428. IDVi006-A-1 (UBAP1L-3225_CRC2)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinal dystrophy

  3429. IDVi006-A-2 (UBAP1L-3225_CRB22)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinal dystrophy

  3430. IDVi006-A-3 (UBAP1L-3225_CRB112)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinal dystrophy

  3431. IGGi001-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Obsolete sotos syndrome 1

  3432. IGGi001-B

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Obsolete sotos syndrome 1

  3433. IGGi002-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Cystic fibrosis

  3434. IGGi003-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Sotos syndrome

  3435. IGGi004-A (ZEB2 case 1)

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Mowat-wilson syndrome

  3436. IGGi005-A (ZEB2 case 2)

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Mowat-wilson syndrome

  3437. IGGi006-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Caprin1

  3438. IGGi007-A (iPSC hNECWT4 CLONE1)

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Normal (average)

  3439. IGGi008-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Mowat-wilson syndrome

  3440. IGGi009-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Mowat-wilson syndrome

  3441. IGIBi001-A (SCP28)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Sickle cell anemia

  3442. IGIBi002-A

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Beta-thalassemia

  3443. IGIBi011-A (GOC-13)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Spinocerebellar ataxia type 12

  3444. IGIBi012-A (FA-hiPSC_001)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Friedreich ataxia

  3445. IGIBi013-A (FA_hiPSC_002)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Friedreich ataxia

  3446. IGIBi016-A (FA-hiPSC_005)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Friedreich ataxia

  3447. IGIBi017-A (CT_hiPSC_001)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3448. IGIBi018-A

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Rubinstein taybi like syndrome

  3449. IGIBi019-A (iPSC V2b)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3450. IGIBi020-A (iPSC V1b)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3451. IGIBi021-A (iPSC V3b)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3452. IGIBi022-A (iPSC V2c)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3453. IGIBi023-A (iPSC V1c)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3454. IGIBi024-A (iPSC V3c)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3455. IGIBi025-A (iPSC V3a)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  3456. IGIBi026-A (BKWD01)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Wilson disease

  3457. IIMCBi003-A (K-Pic1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)
    Disease:

    Normal (average)

  3458. IIMCBi003-B (K-Pic2)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)
    Disease:

    Normal (average)

  3459. IIMCBi004-A (PM-H1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)

  3460. IIMCBi005-A (EM-K3)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)

  3461. IIMCBi006-A (M-T1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)
    Disease:

    Huntington's disease

  3462. IIMCBi006-B (M-T2)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)
    Disease:

    Huntington's disease

  3463. IIMCBi007-A (jK-N1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)
    Disease:

    Normal (average)

  3464. IIMCBi008-A (jHD-V1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)

  3465. IMAGINi002-A (IMAGINE002)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Epidermolysis bullosa

  3466. IMAGINi003-A (IMAGINE003)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Epidermolysis bullosa

  3467. IMAGINi004-A (IMAGINE004)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  3468. IMAGINi005-A (IMAGINE005)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  3469. IMAGINi013-A (IMAGINE013)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  3470. IMAGINi020-A (IMAGINE020)

    France Imagine Institute / INSERM U1163 (IMAGIN)

  3471. IMAGINi021-A (IMAGINE021)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  3472. IMAGINi022-A (IMAGINE022)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Waardenburg syndrome

  3473. IMAGINi039-A (IMAGINE039)

    France Imagine Institute / INSERM U1163 (IMAGIN)

  3474. IMAGINi045-A (IMAGINE045)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Loeys-dietz syndrome

  3475. IMAGINi050-A (IMAGINE050)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Tay-sachs disease

  3476. IMAGINi051-A (IMAGINE051)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Tay-sachs disease

  3477. IMAGINi052-A (IMAGINE052)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Tay-sachs disease

  3478. IMAGINi070-A (IMAGINE070)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Meier-gorlin syndrome 1

  3479. IMBAi001-A (SCCF-176J clone#1 and HD.1 ARID1B+/+ clone 3a (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3480. IMBAi001-A-1 (HD.1 ARID1B+/- clone 3b (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3481. IMBAi001-B (SCCF-176J clone#2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3482. IMBAi002-A (SCCF-177J clone#8)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3483. IMBAi002-B (SCCF-177J clone#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3484. IMBAi002-C (SCCF-177J clone#6)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3485. IMBAi003-A (SCCF-178J clone#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3486. IMBAi003-B (SCCF-178J clone#6)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3487. IMBAi004-A (SCCF-733J clone#1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3488. IMBAi004-B (SCCF-733J clone#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3489. IMBAi004-C (SCCF-733J clone#17)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3490. IMBAi005-A (SCCF-734J clone#2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3491. IMBAi005-B (SCCF-734J clone#3)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3492. IMBAi005-C (SCCF-734J clone#10)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3493. IMBAi006-A (SCCF-735J clone#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3494. IMBAi006-B (SCCF-735J clone#17)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3495. IMBAi006-C (SCCF-735J clone#20)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3496. IMBAi007-A (SCCF-180J clone#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3497. IMBAi007-B (SCCF-180J clone#11)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3498. IMBAi007-C (SCCF-180J clone#21)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3499. IMBAi008-A (SCCF-181J clone#16)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3500. IMBAi008-B (SCCF-181J clone#20)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3501. IMBAi008-C (SCCF-181J clone#24)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3502. IMBAi009-A (SCCF-179J clone#13)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3503. IMBAi009-B (SCCF-179J clone#15)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3504. IMBAi009-C (SCCF-179J clone#18)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3505. IMBAi010-A (SCCF-2298J clone#1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3506. IMBAi010-B (SCCF-2298J clone#2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3507. IMBAi010-C (SCCF-2298J clone#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3508. IMBAi011-A (SCCF-736J clone#1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3509. IMBAi011-B (SCCF-736J clone#6)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3510. IMBAi011-C (SCCF-736J clone#8)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3511. IMBAi012-A (DBA 13j #1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  3512. IMBAi013-A (DBA 14J #2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Diamond-blackfan anemia 1

  3513. IMBAi014-A (DBA 15J #3)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Diamond-blackfan anemia 1

  3514. IMBAi015-A (DBA 16J #1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Diamond-blackfan anemia 1

  3515. IMBAi016-A (B001-ARID1B#10 and Pat.1 ARID1B+/- clone 1a (XY))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3516. IMBAi017-A (B002-ARID1B#8 and Pat.2 ARID1B+/- clone 2a (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3517. IMBAi017-A-1 (Pat.2 ARID1B+/+ clone 2c (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3518. IMBAi017-A-2 (Pat.2 ARID1B+/+ clone 2d (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3519. IMBAi017-A-3 (Pat.2 ARID1B+/- clone 2b (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  3520. IMBAi018-A (622_DS04 #1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Dravet syndrome

  3521. IMBAi019-A (623_DS22 #10)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Dravet syndrome

  3522. IMBAi020-A (624_DS40 #8)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Dravet syndrome

  3523. IMBAi020-B (624_DS40 #3)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Dravet syndrome

  3524. IMBAi021-A (TSC107J #5 and TSC#14 clone 107J#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  3525. IMBAi022-A (TSC112#4 and TSC#24 clone 112#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  3526. IMBAi022-A-1 (TSC112#4r2c4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  3527. IMBAi023-A (TSC#5 clone 32S and TSCp5#32S)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  3528. IMBAi023-B (TSC#5 clone 30S, TSCp5#30S and TSC98#30S)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  3529. IMBPASi001-A (iPSC-WFS1-#1)

    Poland Institute of Medical Biology of Polish Academy of Sciences (IMBPAS)
    Disease:

    Wolfram syndrome 1

  3530. ISFi001-A-1

    Switzerland Institute of Medical Genetics (IMG)
    Disease:

    Joubert syndrome 5

  3531. ISFi001-A-2

    Switzerland Institute of Medical Genetics (IMG)
    Disease:

    Joubert syndrome

  3532. IMGi003-A (COQ4_Phe146Cys_Cl.1.1)

    Switzerland Institute of Medical Genetics (IMG)
    Disease:

    Primary coenzyme q10 deficiency 7

  3533. IMGTi001-A (iTAF5-29)

    Russia Research Institute of Medical Genetics, TNMRC (IMGT)
    Disease:

    Phelan-mcdermid syndrome

  3534. IMGTi001-B (iTAF5-32)

    Russia Research Institute of Medical Genetics, TNMRC (IMGT)
    Disease:

    Phelan-mcdermid syndrome

  3535. IMGTi003-A (iTAF6-6)

    Russia Research Institute of Medical Genetics, TNMRC (IMGT)
    Disease:

    Ring chromosome 13 syndrome

  3536. IMOi001-A (STGD PBiPS1-SV4F-1)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3537. IMOi002-A (STGD PBiPS2-SV4F-1)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3538. IMOi003-A (STGD PBiPS3-SV4F-10)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3539. IMOi004-A (STGD PBiPS4-SV4F-1)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3540. IMOi005-A (STGD PBiPS5-SV4F-2)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3541. IMOi006-A (STGD PBiPS6-SV4F-2)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  3542. IMRi002-A

    Malaysia Institute for Medical Research (IMR)
    Disease:

    Normal (average)

  3543. INDBi001-A (INDB5.2.14)

    Germany Institute for Neuroanatomy and Developmental Biology, University of Tuebingen (INDB)
    Disease:

    Normal (average)

  3544. INEUi002-A (iPSC-FN2.1, FN2.1 and FN2.1 WT)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Normal (average)

  3545. INEUi002-A-1 (PKP2 S140F)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Cardiomyopathy

  3546. INEUi002-A-2 (PKP2 KO)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Cardiomyopathy

  3547. INEUi002-A-7 (PKG-KO)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Cardiomyopathy

  3548. INEUi003-A (FHL1-T)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Muscular dystrophy

  3549. INEUi004-A (FHL1-V)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Muscular dystrophy

  3550. INEUi005-A (FOXA2S229*-iPSCs)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Non-acquired combined pituitary hormone deficiency

  3551. IRMBi001-A-1 (AD-PS1-ISO1)

    France Institute for Neurosciences of Montpellier (INM)
    Disease:

    Obsolete_alzheimer's disease

  3552. IRMBi001-A-2 (AD-PS1-ISO2)

    France Institute for Neurosciences of Montpellier (INM)
    Disease:

    Obsolete_alzheimer's disease

  3553. INNDSUi001-A (186-Nml-F-24)

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Normal (average)

  3554. INNDSUi002-A (21-013)

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Multiple acyl-coa dehydrogenase deficiency

  3555. INNDSUi003-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Becker muscular dystrophy

  3556. INNDSUi004-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Nemaline myopathy

  3557. INNDSUi005-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Normal (average)

  3558. INNDSUi006-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Myotonic dystrophy type 1

  3559. INNDSUi007-A (ZHH-KD)

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Kennedy disease

  3560. INNDSUi008-A (JKL-SCA)

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Machado-joseph disease

  3561. INNDSUi009-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Amyotrophic lateral sclerosis

  3562. INNDSUi010-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Dermatomyositis

  3563. INNDSUi011-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Peripheral neuropathy

  3564. INSAi001-A

    Portugal Instituto Nacional de Saude Ricardo Jorge (INSA)
    Disease:

    Gaucher disease type 3

  3565. INSAi002-A

    Portugal Instituto Nacional de Saude Ricardo Jorge (INSA)
    Disease:

    Fabry disease

  3566. INSAi003-A

    Portugal Instituto Nacional de Saude Ricardo Jorge (INSA)
    Disease:

    Mucolipidosis type ii

  3567. TMOi001-A-11

    France INSERM (INSRM)
    Disease:

    Cardiomyopathy

  3568. INSRMi002-A (PC117_c2)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  3569. INSRMi003-A (PC128_c5)

    France INSERM (INSRM)
    Disease:

    Normal (average)

  3570. INSRMi004-A (PC118_c7)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  3571. INSRMi005-A (PC119_c7)

    France INSERM (INSRM)
    Disease:

    Normal (average)

  3572. INSRMi006-A (PC131_c8)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  3573. INSRMi007-A (pc132-c4)

    France INSERM (INSRM)
    Disease:

    Normal (average)

  3574. INSRMi012-C (PC173T19)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  3575. INSRMi013-A (PC179c1)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  3576. INSRMi014-A

    France INSERM (INSRM)

  3577. INSRMi015-A

    France INSERM (INSRM)
    Disease:

    Long qt syndrome

  3578. INSRMi019-A (PC129K8)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  3579. INSRMi020-A (PC130k2c)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  3580. INSRMi021-A (PC177 3c14)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  3581. IOBi001-A (F49B7 and 01F49i-N-B7)

    Switzerland Institute of Molecular and Clinical Ophthalmology Basel (IOB) (IOB)
    Disease:

    Normal (average)

  3582. IOCVi002-A (iPSC-FOXE3)

    Mexico Institute of Ophthalmology "Conde de Valenciana" (IOCV)

  3583. IPi001-A (iPSC-healthy-AFC-001)

    France Institut Pasteur (IP)
    Disease:

    Normal (average)

  3584. IPi001-B (iPSC-healthy-AFC-002)

    France Institut Pasteur (IP)
    Disease:

    Normal (average)

  3585. IPi001-C (iPSC-healthy-AFC-003)

    France Institut Pasteur (IP)
    Disease:

    Normal (average)

  3586. IPi002-A (iPSC-MARCH-AFC-001)

    France Institut Pasteur (IP)
    Disease:

    Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome

  3587. IPi002-B (iPSC-MARCH-AFC-002)

    France Institut Pasteur (IP)
    Disease:

    Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome

  3588. IPi002-C (iPSC-MARCH-AFC-003)

    France Institut Pasteur (IP)
    Disease:

    Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome

  3589. IPBi001-A (IPB-HD-001)

    South Korea iPSBIO (IPB)
    Disease:

    Huntington disease

  3590. IPBi002-A (IPB-HD-002)

    South Korea iPSBIO (IPB)
    Disease:

    Huntington disease

  3591. IPBi003-A (IPB-HD-003)

    South Korea iPSBIO (IPB)
    Disease:

    Huntington disease

  3592. IPBi004-A (IPB-HD-004)

    South Korea iPSBIO (IPB)
    Disease:

    Huntington disease

  3593. IPBi101-A (IPB-WT-001)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3594. IPBi102-A (IPB-WT-002)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3595. IPBi103-A (IPB-WT-003)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3596. IPBi104-A (IPB-WT-004-LOY)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3597. IPBi104-B (IPB-WT-004)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3598. IPBi105-A (IPB-WT-005)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3599. IPBi106-A (IPB-WT-006)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3600. IPBi107-A (IPB-WT-007)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3601. IPBi108-A (IPB-WT-008)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3602. IPBi109-A (IPB-WT-009)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3603. IPBi110-A (IPB-WT-010)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3604. IPBi111-A (IPB-WT-011)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3605. IPBi112-A (IPB-WT-012)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3606. IPBi113-A (IPB-WT-013)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3607. IPBi114-A (IPB-WT-014)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3608. IPBi115-A (IPB-WT-015)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3609. IPBi116-A (IPB-WT-016)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3610. IPBi117-A (IPB-WT-017)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3611. IPBi118-A (IPB-WT-018)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3612. IPBi119-A (IPB-WT-019)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3613. IPBi124-A (IPB-WT-024)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3614. IPBi126-A (IPB-WT-026)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3615. IPBi128-A (IPB-WT-028)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3616. IPBi129-A (IPB-WT-029)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  3617. IPSCi001-A (IPSC-087-3)

    Taiwan iPSC Core (IPSC)
    Disease:

    Occult macular dystrophy

  3618. IPSCZHi001-A (GM769_S6)

    Switzerland iPSCore Zurich (IPSCZH)
    Disease:

    Periventricular nodular heterotopia

  3619. IPTi001-A (15M0008)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  3620. IPTi002-A (15F0009)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  3621. IPTi003-A (15M0010)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  3622. IPTi004-A (15M0011)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  3623. IPTi005-A (16M0064)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal (average)

  3624. IPTi006-A (16M0065)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal (average)

  3625. IPTi007-A (16F0066)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal (average)

  3626. IRDWCHi001-A

    China Institute of Rare Diseases (IRDWCH)
    Disease:

    Hearing loss

  3627. IRFMNi001-A (iPS clone IV)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal (average)

  3628. IRFMNi001-B (iPS clone XI)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal (average)

  3629. IRFMNi001-B-1 (Clone XI CIITAKO)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal (average)

  3630. IRFMNi001-B-2 (CIone M CIITAKO-B2MKO)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal (average)

  3631. IRFMNi002-A (PRM#14)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Focal segmental glomerulosclerosis

  3632. IRFMNi002-B (PRM#18)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Focal segmental glomerulosclerosis

  3633. IRFMNi003-A

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal (average)

  3634. IRFMNi003-A-1 (KO PKD2#17)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Autosomal dominant polycystic kidney disease

  3635. IRFMNi003-A-2 (KO PKD2#36)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Autosomal dominant polycystic kidney disease

  3636. IRFMNi003-A-3 (KO PKD1#16)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Autosomal dominant polycystic kidney disease

  3637. IRFMNi003-A-4 (KO PKD1#5)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Autosomal dominant polycystic kidney disease

  3638. IRMBi001-A (AD-PS1 hiPSC)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Obsolete_alzheimer's disease

  3639. IRMBi002-A (AD-APP hiPSC)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Obsolete_alzheimer's disease

  3640. IRMBi003-A (CT1)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Normal (average)

  3641. IRMBi003-B

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Normal (average)

  3642. IRMBi004-A (CT4)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Normal (average)

  3643. IRMBi005-A (SAD)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Alzheimer disease

  3644. ISCRMi001-A (3-0062 and DSP Leu462fs)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  3645. ISFi001-A (HMGU1 and #1)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Normal (average)

  3646. ISFi002-A (HMGU12)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Normal (average)

  3647. ISFi003-A (D2)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Van maldergem syndrome 1

  3648. ISFi004-A (F1)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Van maldergem syndrome 1

  3649. ISMMSi001-A (SAMEA104275576 and MFS44-E)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  3650. UCSFi001-A-79 (MSE2336A and WTC11-AAVS1-GCamp6s C1)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3651. ISMMSi001-B (SAMEA104275577 and MFS44-16)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  3652. ISMMSi002-A (SAMEA104275578 and MFS60-12)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  3653. ISMMSi002-B (MFS60-3-1 and SAMEA104276575)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  3654. ISMMSi004-A (MSN01-02S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3655. ISMMSi005-A (MSN02-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3656. ISMMSi006-A (MSN03-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3657. ISMMSi007-A (MSN04-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3658. ISMMSi008-A (MSN05-01R)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3659. ISMMSi009-A (MSN06-07R)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3660. ISMMSi010-A (MSN07-07S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3661. ISMMSi011-A (MSN08-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3662. ISMMSi012-A (MSN09-02S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3663. ISMMSi013-A (MSN10-07S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3664. ISMMSi014-A (MSN11-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3665. ISMMSi015-A (MSN12-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3666. ISMMSi016-A (MSN13-03S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3667. ISMMSi017-A (MSN14-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3668. ISMMSi017-B (MSN14-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3669. ISMMSi017-C (MSN14-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3670. ISMMSi018-A (MSN15-31S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3671. ISMMSi019-A (MSN16-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3672. ISMMSi020-A (MSN17-07S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3673. ISMMSi021-A (MSN18-03S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3674. ISMMSi022-A (MSN19-07S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3675. ISMMSi023-A (MSN20-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3676. ISMMSi024-A (MSN21-08S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3677. ISMMSi025-A (MSN22-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3678. ISMMSi026-A (MSN23-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3679. ISMMSi027-A (MSN24-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3680. ISMMSi028-A (MSN25-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3681. ISMMSi028-B (MSN25-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3682. ISMMSi028-C (MSN25-09S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3683. ISMMSi029-A (MSN26-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3684. ISMMSi030-A (MSN27-03S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3685. ISMMSi031-A (MSN28-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3686. ISMMSi032-A (MSN29-03S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3687. ISMMSi033-A (MSN30-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3688. ISMMSi034-A (MSN31-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3689. ISMMSi035-A (MSN32-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3690. ISMMSi036-A (MSN33-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3691. ISMMSi037-A (MSN34-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3692. ISMMSi038-A (MSN35-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3693. ISMMSi039-A (MSN36-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3694. ISMMSi040-A (MSN37-01S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3695. ISMMSi041-A (MSN38-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3696. ISMMSi042-A (MSN39-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3697. ISMMSi043-A (MSN40-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3698. ISMMSi044-A (PLNR14del-1BC1)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  3699. ISMMSi045-A (PLNR14del-2BC4)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  3700. ISMMSi046-A (PLN-R14del-3BC7)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  3701. ISMMSi047-A (PLN-R14del-4AC4)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  3702. ISMMSi048-A (PLN-R14del-5BC4)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  3703. ISMMSi049-A (PLN-1CC1)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3704. ISMMSi050-A (PLN-4CC4)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3705. ISMMSi051-A (PLN-5AC2)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal (average)

  3706. ISMMSi060-A (CSI2101A)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Combined oxidative phosphorylation defect type 25

  3707. ISTEMi001-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease type iii

  3708. ISTEMi002-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease type iii

  3709. ISTEMi003-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease type iii

  3710. 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

  3711. ISTEMi005-A (CAC2, 9881-clC and 9881cloneC)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Congenital myopathy 18

  3712. 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

  3713. 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

  3714. ISTEMi008-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease ii

  3715. ISTEMi009-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease ii

  3716. ISTEMi010-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease ii

  3717. ISTEMi011-A (WDR45 BPAN01 c02)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3718. ISTEMi011-B (WDR45 BPAN01 c09)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3719. ISTEMi012-A (WDR45 BPAN02 c04)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3720. ISTEMi013-A (WDR45 BPAN03 c05)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3721. ISTEMi013-B (WDR45 BPAN03 c12)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3722. ISTEMi014-A (WDR45 BPAN04 c04)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  3723. ISTEMi015-A (4603c53)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Normal (average)

  3724. ITBi001-A (EP1A)

    Italy Institute for Biomedical Technologies (ITB)
    Disease:

    Developmental and epileptic encephalopathy 85 with or without midline brain defects

  3725. ITBi002-A (EP2B)

    Italy Institute for Biomedical Technologies (ITB)
    Disease:

    Developmental and epileptic encephalopathy 85 with or without midline brain defects

  3726. ITXi001-A (hERG CT Cl9)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3727. ITXi001-A-1 (GPR146KO Cl2)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3728. ITXi002-A (IRX5-Wt and H166Wt C09)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3729. ITXi002-A-1 (CRISPR-2 IRX5 F12 Het and IRX5-Het)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3730. ITXi002-A-2 (CRISPR-2 IRX5 D8 KO and IRX5-KO)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3731. ITXi002-A-3 (IRX5-KI and CRISPR-3 IRX5 F6 KI)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3732. ITXi003-A (MS368)

    France l’institut du thorax (ITX)
    Disease:

    Long qt syndrome

  3733. ITXi004-A (MS381)

    France l’institut du thorax (ITX)
    Disease:

    Long qt syndrome

  3734. ITXi005-A (MS573)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3735. ITXi006-A (WT8288)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3736. ITXi006-A-1 (IM-R406W)

    France l’institut du thorax (ITX)
    Disease:

    Desminopathy

  3737. ITXi007-A (202CT)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3738. ITXi008-A (SD378M)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  3739. ITXi009-A (CPVT068)

    France l’institut du thorax (ITX)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3740. ITXi010-A (CPVT249)

    France l’institut du thorax (ITX)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3741. ITXi011-A (CPVT033)

    France l’institut du thorax (ITX)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  3742. ITXi012-A (Lp(a) Cl23)

    France l’institut du thorax (ITX)
    Disease:

    Hyperlipoproteinemia

  3743. ITXi013-A (PT-R406W)

    France l’institut du thorax (ITX)
    Disease:

    Desminopathy

  3744. ITXi013-B (IC-R406)

    France l’institut du thorax (ITX)
    Disease:

    Desminopathy

  3745. IUFi002-A

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Leigh syndrome

  3746. WTSIi018-B-19

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Loss of function gene mutation

  3747. WTSIi018-B-20

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Loss of function gene mutation

  3748. WTSIi018-B-28 (DU411)

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Duchenne muscular dystrophy

  3749. WTSIi018-B-29 (DU414)

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Duchenne muscular dystrophy

  3750. WTSIi018-B-30 (DU434)

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Xeroderma pigmentosum group a

  3751. IUFi020-A (DU372r)

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Autoimmune encephalitis

  3752. WTSIi018-B-12 (KOLF2.1J)

    United Kingdom Jackson Laboratories (JAX)
    Disease:

    Normal (average)

  3753. JHUi005-A (HFD1)

    United States Johns Hopkins University (JHU)
    Disease:

    Marfan syndrome

  3754. JHUi006-A (HFD2 Clone 11)

    United States Johns Hopkins University (JHU)
    Disease:

    Marfan syndrome

  3755. JHUi007-A (i0195, Clone 5)

    United States Johns Hopkins University (JHU)
    Disease:

    Ehlers-danlos syndrome, vascular type

  3756. JHUi007-A-1 (i0195 SubClone D8)

    United States Johns Hopkins University (JHU)
    Disease:

    Ehlers-danlos syndrome, vascular type

  3757. JHUi008-A (JHU001, clone 2)

    United States Johns Hopkins University (JHU)
    Disease:

    Normal (average)

  3758. JHUi009-A (JHU004 Clone 3)

    United States Johns Hopkins University (JHU)
    Disease:

    Ehlers-danlos syndrome, vascular type

  3759. JHUi009-A-1 (JHU004, Clone F6)

    United States Johns Hopkins University (JHU)
    Disease:

    Ehlers-danlos syndrome, vascular type

  3760. JHUi010-A (JHU013, Clone 2)

    United States Johns Hopkins University (JHU)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  3761. JNCHi002-A (JNCHi002-A)

    China Jinan children's Hospital (JNCH)
    Disease:

    Familial hypercholesterolemia

  3762. JNMUi001-A (JNMUi001-A)

    China Jining Medical University (JNMU)
    Disease:

    Schizophrenia

  3763. JNMUi002-A (JNMUi002-A)

    China Jining Medical University (JNMU)
    Disease:

    Schizophrenia

  3764. JNMUi003-A (iPSCs—PB-SCZ-70#-C1P19)

    China Jining Medical University (JNMU)
    Disease:

    Schizophrenia

  3765. JTUi001-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Charge syndrome

  3766. JTUi002-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Waardenburg syndrome

  3767. JTUi003-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Otosclerosis

  3768. JTUi004-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Otosclerosis

  3769. JTUi005-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Neuronal intranuclear inclusion disease

  3770. JTUi007-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

  3771. JUCGRMi001-A (VPS35A4)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3772. JUCGRMi001-B (VPS35A5)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3773. JUCGRMi001-C (VPS35A8)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3774. JUCGRMi002-A (DupA5)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3775. JUCGRMi002-B (DupA13)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3776. JUCGRMi002-C (DupA18)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3777. JUCGRMi003-A (PH13)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson disease

  3778. JUCGRMi004-A (CMTA6)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Charcot-marie-tooth disease

  3779. JUCGRMi005-A (JA5)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Normal (average)

  3780. JUCGRMi006-A (JB6)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Normal (average)

  3781. JUCGRMi007-A (MAPTC3)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Frontotemporal dementia

  3782. JUCGRMi007-B (MAPTC5)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Frontotemporal dementia

  3783. JUCGRMi007-C (MAPTC9)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Frontotemporal dementia

  3784. JUCTCi018-A

    Jordan the University of Jordan / Cell Therapy center (JUCTC)
    Disease:

    Charcot-marie-tooth disease

  3785. JUCTCi019-A

    Jordan the University of Jordan / Cell Therapy center (JUCTC)
    Disease:

    Charcot-marie-tooth disease type 2

  3786. JUFMDOi007-A

    Japan Juntendo University Faculty of Medicine, Department of Otorhinolaryngology (JUFMDO)
    Disease:

    Ush2a

  3787. JUFMDOi008-A (CP009)

    Japan Juntendo University Faculty of Medicine, Department of Otorhinolaryngology (JUFMDO)
    Disease:

    Autosomal recessive nonsyndromic deafness 12

  3788. KAIMRCi002-A (HLA-iPSC#1)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Normal (average)

  3789. KAIMRCi002-B (HLA-iPSC#2)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Normal (average)

  3790. KAIMRCi003-A (DRVT-iPSC#1)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Dravet syndrome

  3791. KAIMRCi003-B (DRVT-iPSC#2)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Dravet syndrome

  3792. KAIMRCi004-A (BTBGD-iPSC#1)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Biotin-thiamine-responsive basal ganglia disease

  3793. KAIMRCi004-B (BTBGD-iPSC#2)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Biotin-thiamine-responsive basal ganglia disease

  3794. KAUSTi001-A (KS7-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3795. KAUSTi001-B (KS7-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3796. KAUSTi003-A (KS1-iPSC#D)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3797. KAUSTi004-A (HM-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  3798. KAUSTi004-B (HM-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  3799. KAUSTi005-A (HB-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  3800. KAUSTi005-B (HB-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  3801. KAUSTi005-C (HB-iPSC#C)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal (average)

  3802. KAUSTi006-A (KS6-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3803. KAUSTi006-B (KS6-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3804. KAUSTi007-A (KS2-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3805. KAUSTi007-B (KS2-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3806. KAUSTi008-A (KS4-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3807. KAUSTi008-B (KS4-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3808. KAUSTi008-C (KS4-iPSC#C)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3809. KAUSTi008-D (KS4-iPSC#D)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3810. KAUSTi008-E (KS4-iPSC#E)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3811. KAUSTi008-F (KS4-iPSC#F)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3812. KAUSTi008-G (KS4-iPSC#G)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3813. KAUSTi009-A (KS3-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3814. KAUSTi009-B (KS3-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3815. KAUSTi010-A (KS5-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3816. KAUSTi010-B (KS5-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  3817. KAUSTi011-A (iPSC-GLP1R-KO-C1)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Developmental and epileptic encephalopathy

  3818. KAUSTi011-B (iPSC-GLP1R-KO-H4)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Developmental and epileptic encephalopathy

  3819. KCGMHi001-A (KCGMH-CEP85L-K303-A4)

    Taiwan Kaohsiung Chang Gung Memorial Hospital (KCGMH)
    Disease:

    Lissencephaly

  3820. KCGMHi002-A (KCGMH-MAST1-K2271-A1)

    Taiwan Kaohsiung Chang Gung Memorial Hospital (KCGMH)
    Disease:

    Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations

  3821. KCGMHi003-A (KCGMH-SCA8-K3143-A4)

    Taiwan Kaohsiung Chang Gung Memorial Hospital (KCGMH)
    Disease:

    Spinocerebellar ataxia type 8

  3822. KCLi001-A (iOP118)

    United Kingdom King's College London (KCL)
    Disease:

    Atopic eczema

  3823. KCLi002-A (iOP107)

    United Kingdom King's College London (KCL)
    Disease:

    Atopic eczema

  3824. KCLi003-A (iOP101)

    United Kingdom King's College London (KCL)
    Disease:

    Atopic eczema

  3825. KEIOi001-A (SM4-4-5)

    Japan Keio University (KEIO)
    Disease:

    Amyotrophic lateral sclerosis type 10

  3826. KEIOi005-A (KAD-0001 and EK-0076)

    Japan Keio University (KEIO)
    Disease:

    Alzheimer's disease

  3827. KEIOi006-A (RPC771-EA)

    Japan Keio University (KEIO)
    Disease:

    Normal (average)

  3828. KEIUi002-A (KOMENT-A)

    Japan Keio University (KEIU)
    Disease:

    Normal (average)

  3829. KEIUi003-A (KOMENT-B)

    Japan Keio University (KEIU)
    Disease:

    Normal (average)

  3830. KEIUi004-A (EYA4-1)

    Japan Keio University (KEIU)
    Disease:

    Hearing loss

  3831. KEIUi005-A (EYA4-2)

    Japan Keio University (KEIU)
    Disease:

    Hearing loss

  3832. KEIUi006-A (EYA4-3)

    Japan Keio University (KEIU)
    Disease:

    Hearing loss

  3833. KEIUi007-A (EYA4-4)

    Japan Keio University (KEIU)
    Disease:

    Hearing loss

  3834. KEIUi008-A (A1555G)

    Japan Keio University (KEIU)
    Disease:

    Hearing loss

  3835. KGUi001-A (AR1023)

    Germany Department of Psychiatry, Psychotherapy and Psychosomatic Medicine, University Hospital, Goethe University of Frankfurt/Main (KGU)
    Disease:

    Obsolete_bipolar disorder

  3836. KGUi002-A (AR1034)

    Germany Department of Psychiatry, Psychotherapy and Psychosomatic Medicine, University Hospital, Goethe University of Frankfurt/Main (KGU)
    Disease:

    Obsolete_bipolar disorder

  3837. KKUi002-A (PD-iPSC)

    South Korea School of medicine, Konkuk University (KKU)
    Disease:

    Normal (average)

  3838. KLRMMEi001-A

    China Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University. (KLRMME)
    Disease:

    Retinitis pigmentosa

  3839. KLRMMEi002-A

    China Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University. (KLRMME)
    Disease:

    Usher syndrome

  3840. KLRMMEi003-A

    China Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University. (KLRMME)
    Disease:

    Usher syndrome

  3841. KMUGMCi001-A (KMUGMCi001ACVRL1)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic

  3842. KMUGMCi002-A (KMUGMCi002NIPBL)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Cornelia de lange syndrome

  3843. KMUGMCi003-A (KMUGMCi003ERCC2 and KN610)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Trichothiodystrophy 1, photosensitive

  3844. KMUGMCi004-A (KMUGMCi004APC and KN615)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Familial adenomatous polyposis

  3845. KMUGMCi005-A (KMUGMCi005TMC8 and KN627)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Epidermodysplasia verruciformis

  3846. KMUGMCi006-A (TS271 #12 WT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  3847. KMUGMCi006-B (TS271 #5 MT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  3848. KMUGMCi006-C (TS271 #21 WT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  3849. KMUGMCi006-D (TS271 #23 WT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  3850. KMUGMCi006-E (TS271 #4 MT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  3851. KMUGMCi006-F (TS271 #20 MT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  3852. KMUGMCi007-A (KMUGMCi007PEPD and KN649)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Prolidase deficiency

  3853. KMUGMCi008-A (KN695 KAT6B and KN695)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Ohdo syndrome

  3854. KMUGMCi009-A (KN686 and KN686 MED12)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Blepharophimosis - intellectual disability syndrome, mkb type

  3855. KMUGMCi010-A (KN687B and KN687B MED12)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Blepharophimosis - intellectual disability syndrome, mkb type

  3856. KRIBBi005-A (CB-iPS-C7)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    Normal (average)

  3857. KRIBBi009-A (KRIBB-BC15)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    Normal (average)

  3858. KRIBBi010-A (XLRS_R141C)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    X-linked retinoschisis

  3859. KRIBBi011-A (XLRS_G44fs)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    X-linked retinoschisis

  3860. KRIBBi012-A (XLRS_E72K)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    X-linked retinoschisis

  3861. KSCBi001-A (hUSiPS2)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3862. KSCBi002-A (hFSiPS1)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3863. KSCBi002-B (hFmiPS1)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3864. KSCBi002-B-1 (hFmiPS2)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3865. KSCBi003-A (hAdMSiPS1 and hAdMSCiPS1)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3866. KSCBi005-A (CMC-hiPSC-003)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3867. KSCBi005-A-1 (CMC-hiPSC-003(Nestin-GFP) and CMC-003i-Nestin.EGFP)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3868. KSCBi005-A-2 (CMC-hiPSC-003(Sox1-GFP) and CMC-003i-Sox1.EGFP)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3869. KSCBi005-A-3 (CMC-003i-Pdx1.EGFP and CMC-hiPSC-003(PDX1-GFP))

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3870. KSCBi005-A-7

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3871. KSCBi006-A (KNIH-OI001i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Osteogenesis imperfecta type 1

  3872. KSCBi007-A (KNIH-PWS001i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Prader-willi syndrome

  3873. KSCBi010-A (DKH005i-A and DKHi005-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Senior-loken syndrome

  3874. KSCBi011-A (DKHi090-A and DKH090i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Leber congenital amaurosis

  3875. KSCBi012-A (NU01-EiPS07)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3876. KSCBi016-A (LQT06-hiPSC, DPHCi06 and KNIH-LQT6-hiPSC)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Long qt syndrome

  3877. KSCBi017-A (PB01-EiPS21)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3878. KSCBi017-A-1 (PB01-EiPS21_GATA6-EGFP)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3879. KSCBi017-A-2

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3880. KSCBi017-A-4

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  3881. KSCBi025-A (DPHKi08 and KNIH-LQT37-hiPSC)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Brugada syndrome

  3882. KSCBi026-A (KNIH-LQT13-hiPSC, DPHCi13 and LQT-13)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Atrial fibrillation

  3883. BIONi010-C-56 (BIONi010-C-A713T-C25)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  3884. BIONi010-C-57 (BIONi010-C-A713T-C42)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  3885. BIONi010-C-58 (BIONi010-C-A713T-C1)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  3886. BIONi010-C-59 (BIONi010-C-A713T-C33)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  3887. BIONi010-C-60 (BIONi010-C-R589C-C7)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  3888. BIONi010-C-61 (BIONi010-C-R589C-C16)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  3889. BIONi010-C-62 (BIONi010-C-R589C-C5)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  3890. BIONi010-C-63 (BIONi010-C-R589C-C9)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  3891. KUi012-A (JM09)

    Denmark University of Copenhagen (KU)
    Disease:

    Normal (average)

  3892. KUi012-A-1 (JM09 GC)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  3893. KUi013-A (SK)

    Denmark University of Copenhagen (KU)
    Disease:

    Normal (average)

  3894. KUi013-A-1 (SK GC)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  3895. KUCFRi005-A

    South Korea Korea University Cell Function Regulation Lab (KUCFR)
    Disease:

    Normal (average)

  3896. KUCFRi005-A-1

    South Korea Korea University Cell Function Regulation Lab (KUCFR)
    Disease:

    African swine fever virus

  3897. KUIFMSi004-A (201B1)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal (average)

  3898. KUIFMSi004-B (201B6)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal (average)

  3899. KUIFMSi004-C (201B7)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal (average)

  3900. KUIFMSi004-D (201B2)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal (average)

  3901. KUIFMSi004-E (201B3)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal (average)

  3902. KUIFMSi009-A (243H1)

    Japan Kyoto University (KUIMS)

  3903. KUIFMSi009-B (243H7)

    Japan Kyoto University (KUIMS)

  3904. KUIFMSi011-A (246G1)

    Japan Kyoto University (KUIMS)

  3905. KUIFMSi011-B (246G3)

    Japan Kyoto University (KUIMS)

  3906. KUIFMSi011-C (246G4)

    Japan Kyoto University (KUIMS)

  3907. KUIFMSi011-D (246G5)

    Japan Kyoto University (KUIMS)

  3908. KUIFMSi011-E (246G6)

    Japan Kyoto University (KUIMS)

  3909. SIGi001-A-21 (SIGi001-AAVS1-FRT)

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  3910. SIGi001-A-22 (SIGi001-ICAM1-GFP)

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  3911. SIGi001-A-23 (SIGi001-HC3x)

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  3912. SIGi001-A-24 (SIGi001-HC3x-ICAM1-GFP)

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  3913. SIGi001-A-25

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  3914. SIGi001-A-26

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  3915. KULi003-A

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  3916. KUMi001-A (KUMi001-A_CML(Ph+))

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Myeloid leukemia, philadelphia-positive

  3917. KUMi002-A (CD34+ CML (Ph-) hiPSCs)

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Chronic myeloid leukemia

  3918. KUMi003-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Acute promyelocytic leukemia

  3919. KUMi004-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Chronic lymphocytic leukemia

  3920. KUMi005-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Multiple myeloma

  3921. KUMi006-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Multiple myeloma

  3922. KUMCi001-A (ALLCD34+)

    South Korea KOREA UNIVERSTY COLLEGE OF MEDICINE (KUMC)
    Disease:

    Acute lymphoblastic leukemia

  3923. KUMCi002-A (MM_CD34+iPSCs)

    South Korea KOREA UNIVERSTY COLLEGE OF MEDICINE (KUMC)
    Disease:

    Multiple myeloma

  3924. LBi001-A (PH-BL-001 Clone 4 and iLB-268bfs4)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3925. LBi001-B (iLB-268bfs9 and PH-BL-001 Clone 9)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3926. LBi002-A (PH-BL-002 Clone 2 and iLB-272bfs2)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3927. LBi002-B (PH-BL-002 Clone 9 and iLB-272bfs9)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3928. LBi003-A (iLB-273bms57 and PH-BL-003 Clone 57)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3929. LBi003-B (PH-BL-003 Clone 61 and iLB-273bms61)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3930. LBi004-A (PH-BL-204 Clone 210 and iLB-278bfs210)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3931. LBi004-B (PH-BL-204 Clone 211 and iLB-278bfs211)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3932. LBi005-A (iLB-293bms257 and PH-BL-411 Clone 257)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3933. LBi005-B (iLB-293bms258 and PH-BL-411 Clone 258)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3934. LBi006-A (PH-BL-102 Clone 16 and iLB-269bms16)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3935. LBi006-B (iLB-269bms8 and PH-BL-102 Clone 8)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3936. LBi007-A (iLB-285bfs98 and PH-BL-406 Clone 98)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3937. LBi007-B (iLB-285bfs99 and PH-BL-406 Clone 99)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3938. LBi008-A (PH-BL-407 Clone 128 and iLB-289bms128)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3939. LBi008-B (iLB-289bms145 and PH-BL-407 Clone 145)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3940. LBi009-A (PH-BL-405 Clone 174 and iLB-284bms174)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3941. LBi009-B (iLB-284bms179 and PH-BL-405 Clone 179)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3942. LBi010-A (PH-BL-403 Clone 275 and iLB-282bfs275)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3943. LBi010-B (iLB-282bfs283 and PH-BL-403 Clone 283)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3944. LBi011-A (PH-BL-004 Clone 14 and iLB-274bfs14)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3945. LBi011-B (PH-BL-004 Clone 17 and iLB-274bfs17)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3946. LBi012-A (iLB-292bms74 and PH-BL-410 Clone 74)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3947. LBi012-B (PH-BL-410 Clone 80 and iLB-292bms80)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3948. LBi013-A (PH-BL-304 Clone 117 and iLB-279bfs117)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3949. LBi014-A (iLB-281bfs191 and PH-BL-402 Clone 191)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3950. LBi014-B (PH-BL-402 Clone 192 and iLB-281bfs192)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3951. LBi015-A (iLB-277bms227 and PH-BL-303 Clone 227)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3952. LBi015-B (iLB-277bms234 and PH-BL-303 Clone 234)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3953. LBi016-A (PH-BL-414 Clone 10 and iLB-296bfs10)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3954. LBi016-B (PH-BL-414 Clone 16 and iLB-296bfs16)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3955. LBi017-A (PH-BL-401 Clone 22 and iLB-280bfs22)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3956. LBi017-B (PH-BL-401 Clone 36 and iLB-280bfs36)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3957. LBi018-A (PH-BL-409 Clone 43 and iLB-291bfs43)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3958. LBi018-B (PH-BL-409 Clone 45 and iLB-291bfs45)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3959. LBi019-A (PH-BL-901 Clone 154 and iLB-275bms154)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3960. LBi019-B (iLB-275bms162 and PH-BL-901 Clone 162)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3961. LBi020-A (iLB-294bms22 and PH-BL-412 Clone 238)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  3962. LBMi001-A (idic(Y))

    China Dongfang Hospital of Xiamen University (LBM)
    Disease:

    Infertility

  3963. LCPHi001-A

    China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)
    Disease:

    Obsolete_parkinson's disease

  3964. LCPHi002-A

    China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)
    Disease:

    Parkinson disease

  3965. LCPHi003-A

    China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)
    Disease:

    Parkinson disease

  3966. LCSBi001-A (VPS35 1_2)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Obsolete_parkinson's disease

  3967. LCSBi002-B (ND40066-clone 7 and ND40066-PINK1/PARK6-ILE368ASN-clone 7)

    United States Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3968. LCSBi002-C (ND40066-clone 8 and ND40066-PINK1/PARK6-ILE368ASN-clone 8)

    United States Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3969. LCSBi004-A (ND29369-clone 1 and ND29369-PARKIN/PRKN/PARK2-R275W-clone 1)

    United States Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3970. 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

  3971. LCSBi008-A (delP and DJ-1-delP)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3972. LCSBi008-A-1 (delP GC13 and DJ-1-delP GC13)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3973. LCSBi009-A (RHOT1_R272Q_clone1_PD)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3974. LCSBi009-A-1 (RHOT1_R272Q_clone18_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3975. LCSBi010-A (RHOT1_R450C_clone5_PD)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3976. LCSBi010-A-1 (RHOT1_R450C_clone6_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3977. LCSBi010-A-2 (RHOT1_R450C_clone10_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3978. LCSBi011-A (RHOT1_T351A_clone1_PD)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3979. LCSBi011-A-1 (RHOT1_T351A_clone25.2_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3980. LCSBi012-A (RHOT1_T610A_clone6_PD)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3981. LCSBi012-A-1 (RHOT1_T610A_clone62.19.37_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3982. LCSBi013-A (GL2)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3983. LCSBi014-A (#89739 and S1 Cl19a)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3984. LCSBi015-A (S2 Cl4 and 89732)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3985. LCSBi016-A (S3 Cl17 and 90812)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3986. LCSBi017-A (M1 Cl6b and #89721)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3987. LCSBi018-A (M2 Cl4 and #90806)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  3988. LEIi004-A

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  3989. LEIi004-A-1

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  3990. LEIi005-A

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  3991. LEIi006-A

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  3992. LEIi019-A (1020ips3)

    Australia Lions Eye Institute (LEI)
    Disease:

    Pattern dystrophy

  3993. LEIi020-A (1049ips2)

    Australia Lions Eye Institute (LEI)
    Disease:

    Usher syndrome type 1b

  3994. LEIi020-B

    Australia Lions Eye Institute (LEI)
    Disease:

    Usher syndrome type 1b

  3995. LEIi021-A (1577ips7)

    Australia Lions Eye Institute (LEI)
    Disease:

    Normal (average)

  3996. LEIi021-B (1577ips9)

    Australia Lions Eye Institute (LEI)
    Disease:

    Normal (average)

  3997. LEIi022-A (CMRIi0032-A-1 and 1765ips1)

    Australia Lions Eye Institute (LEI)
    Disease:

    Normal (average)

  3998. LEIi022-B (1765ips2 and CMRIi0032-A-2)

    Australia Lions Eye Institute (LEI)
    Disease:

    Normal (average)

  3999. LEIi023-A (1150ips4)

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa 11

  4000. LGMi001-A (ALMS1-STBG-1)

    France Medical Genetics Laboratory (LGM)
    Disease:

    Alstrom syndrome

  4001. LIBDi020-A (4001.02)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4002. LIBDi021-A (4002.04)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4003. LIBDi022-A (4003.07)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4004. LIBDi023-A (4004.04)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4005. LIBDi024-A (4005.03)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4006. LIBDi025-A (4006.02)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4007. LIBDi026-A (4007.07)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4008. LIBDi027-A (4008.02)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  4009. LIMFRi001-A (LIMFR-A)

    France University of Limoges (LIMFR)
    Disease:

    Normal (average)

  4010. LNDWCHi001-A (LNDWCH-iPS-PD-PLA2G6–001)

    China Laboratory of Neurodegenerative Disorders (LNDWCH)
    Disease:

    Parkinson disease

  4011. LSCTRi006-A (LSCTR-LiPSC-4 and i4)

    South Korea Laboratory of Stem Cells and Tissue Regeneration (LSCTR)
    Disease:

    Normal (average)

  4012. LSCTRi007-A (LSCTR-LiPSC-5 and i5)

    South Korea Laboratory of Stem Cells and Tissue Regeneration (LSCTR)
    Disease:

    Normal (average)

  4013. UCSFi001-A-72 (FUS-R521G HET 2B10 and LSUHSi004-A-72)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  4014. UCSFi001-A-73 (FUS-R521G HOM 1D9)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  4015. UCSFi001-A-74 (FUS-P525L HET 2D1)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  4016. UCSFi001-A-75 (FUS-P525L HOM 2D2)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  4017. LUi001-A (CALP1.3)

    Latvia University of Latvia (LU)
    Disease:

    Calpain-3-related limb-girdle muscular dystrophy r1

  4018. LUi002-A (CALP2.2)

    Latvia University of Latvia (LU)
    Disease:

    Calpain-3-related limb-girdle muscular dystrophy r1

  4019. LUi003-A (CALP3.1)

    Latvia University of Latvia (LU)
    Disease:

    Calpain-3-related limb-girdle muscular dystrophy r1

  4020. LUBi001-A (PGRN-8310, PGRN8310, RCi195 and RCFB58 c12.5)

    Denmark H. Lundbeck A/S (LUB)
    Disease:

    Frontotemporal dementia

  4021. LUBi001-B (PGRN-8310, RCFB58 c4.4, PGRN8310 and RCi194)

    Denmark H. Lundbeck A/S (LUB)
    Disease:

    Frontotemporal dementia

  4022. LUBi001-C (PGRN-8310, RCFB58 c3.7, RCi200 and PGRN8310)

    Denmark H. Lundbeck A/S (LUB)
    Disease:

    Frontotemporal dementia

  4023. LUEi012-A (iPS-L-2131)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Normal (average)

  4024. LUEi013-A (iPS-L-2135)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Normal (average)

  4025. LUEi014-A (iPS-B-125)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Parkinson disease

  4026. LUEi015-A (iPS-B-11)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Parkinson disease

  4027. LUEi017-A (iPS-L-2122)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Parkinson disease

  4028. LUEi018-A (iPS-L-2124)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Parkinson disease

  4029. LUEi019-A (iPS-L-8172-1)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  4030. LUEi019-B (iPS-L-8172-2)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Beta-propeller protein-associated neurodegeneration

  4031. LUEi020-A (iPS-L9827-6)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  4032. LUEi020-A-1 (iPS-L9827-6_TOR1A_WT-3xFLAG/dGAG)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  4033. LUEi020-A-2 (iPS-L9827-6_TOR1A_WT-3xFLAG/WT-3xFLAG)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  4034. LUEi020-A-3 (iPS-L9827-6_TOR1A_dGAG-3xFLAG/dGAG)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  4035. LUEi020-A-4 (iPS-L9827-6_TOR1A_WT/dGAG-3xFLAG)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  4036. LUMCi001-A (LUMC0054iCTRL02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4037. LUMCi001-B (LUMC0054iCTRL03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4038. LUMCi002-A (113-6 and LUMC0113iATAX06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4039. LUMCi002-B (113-7 and LUMC0113iATAX07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4040. LUMCi002-C (113-8 and LUMC0113iATAX08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4041. LUMCi003-A (114-1 and LUMC0114iCTRL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4042. CRMi003-A-2

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4043. CRMi003-A-3 (Proliving and GMNN-mScarletI Reporter)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4044. LUMCi003-B (114-2 and LUMC0114iCTRL02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4045. LUMCi004-A (LUMC0099iCTRL04)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4046. LUMCi004-A-1 (LU99_AAVS1-bxb-v2)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4047. LUMCi004-A-2 (LU99_CLYBL-bxb-v2)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4048. LUMCi004-A-3 (LUMCi099_XPA_B8)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Xeroderma pigmentosum group a

  4049. LUMCi004-A-4 (LUMCi099_XPC_D10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Xeroderma pigmentosum group c

  4050. LUMCi004-A-5 (LU99_SCN5A-R282H_cis)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Brugada syndrome

  4051. LUMCi004-A-6 (LU99_SCN5A-R282H_trans)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Brugada syndrome

  4052. LUMCi004-A-7 (LU99-04_AAVS-bxb-dual)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4053. LUMCi004-A-8 (LU99 CLYBL-Bxb-v3_Dual and LUMC0099iCLYBL-06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4054. LUMCi004-B (LUMC0030iCTRL12)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4055. LUMCi004-C (LUMC0031iCTRL08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4056. LUMCi007-A (LUMC0151iHD01 and 151-1)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  4057. LUMCi007-B (LUMC0151iHD05 and 151-5)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  4058. LUMCi008-A (152-2 and LUMC0152iHD02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  4059. LUMCi008-B (152-3 and LUMC0152iHD03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  4060. LUMCi008-C (152-4 and LUMC0152iHD04)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  4061. LUMCi013-A (LUMC0133iCTRL06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4062. LUMCi014-A (LUMC0134iCTRL29)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4063. LUMCi015-A (LUMC0135iCTRL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4064. LUMCi016-A (LUMC0136iCTRL09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4065. LUMCi017-A (LUMC0111iALK and LUMC0111iALK07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4066. LUMCi017-A-1 (iso01LUMC0111iALK07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4067. LUMCi017-A-2 (iso02LUMC0111iALK07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4068. LUMCi018-A (LUMC0112iALK and LUMC0112iALK08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4069. LUMCi018-A-1 (iso01LUMC0112iALK08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4070. LUMCi018-A-2 (iso02LUMC0112iALK08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  4071. LUMCi022-A (115-1 and LUMC0115iATAX01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4072. LUMCi022-B (115-2 and LUMC0115iATAX02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4073. LUMCi022-C (115-7 and LUMC0115iATAX07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  4074. LUMCi023-A (LUMC0125iCTRL06 and 125-6)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4075. LUMCi027-A (LUMC0153iPKP03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Arrhythmogenic right ventricular dysplasia 9

  4076. LUMCi027-A-1 (iso01LUMC0153iPKP03 and LUMC0153iPKP03corr#22)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Arrhythmogenic right ventricular dysplasia 9

  4077. LUMCi028-A (LUMC0020iCTRL06 and FLB6)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4078. LUMCi029-A (LUMC0072iCTRL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4079. LUMCi029-A-2 (IsoLUMC0072iENG p.Met1Val-F5)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 1

  4080. LUMCi029-B (LUMC0004iCTRL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4081. LUMCi030-A (LUMC0110iALK04)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Hereditary hemorrhagic telangiectasia

  4082. LUMCi030-A-1 (iso03LUMC0110iALK04)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Hereditary hemorrhagic telangiectasia

  4083. LUMCi030-B (LUMC0110iALK10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Hereditary hemorrhagic telangiectasia

  4084. LUMCi030-B-1 (iso01LUMC0110iALK10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Hereditary hemorrhagic telangiectasia

  4085. LUMCi031-A (LUMC0065iCTRL08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4086. LUMCi039-A (LQT1-1781G/A hiPSC and LUMC0021iKCNQ-30)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Long qt syndrome 1

  4087. LUMCi040-A (LUMC0053iSCN01B)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Brugada syndrome

  4088. LUMCi045-A (LUMC0145iKLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4089. LUMCi045-A-1 (iso01LUMC0145iKLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4090. LUMCi046-A (LUMC0146iKLHL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4091. LUMCi046-A-1 (iso2LUMC0146iKLHL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4092. LUMCi048-A (LUMCi048CTRL-A, 48CTRL-A and 48CTRL-3)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4093. LUMCi048-B (48CTRL-B, LUMCi048CTRL-B and 48CTRL-6)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4094. LUMCi048-C (LUMCi048CTRL-C, 48CTRL-C and 48CTRL-8)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4095. LUMCi049-A (LUMCi049SCA3-A, 49SCA3-A and 49SCA3-1)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4096. LUMCi049-B (LUMCi049SCA3-B, 49SCA3-B and 49SCA3-2)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4097. LUMCi049-C (LUMCi049SCA3-C, 49SCA3-C and 49SCA3-4)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  4098. LUMCi051-A

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 7

  4099. LUMCi051-B

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 7

  4100. LUMCi052-A

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia 7

  4101. LUMCi052-B

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia 7

  4102. LUMCi052-C

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia 7

  4103. LUMCi054-A (CRB1 patient c.3122T>C p.(Met1041Thr) homozygote and LUMC0116iCRB09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  4104. LUMCi054-A-1 (LUMC0116iCRB09 ISO-02, LUMC0116iCRB09 homozygote CRISPR corrected isogenic clone 02 and iso02LUMC0116iCRB09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  4105. LUMCi054-A-2 (LUMC0116iCRB09 ISO-03, LUMC0116iCRB09 heterozygote CRISPR corrected isogenic clone 03 and iso03LUMC0116iCRB09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  4106. 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

  4107. 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

  4108. LUMCi056-A-1 (LUMC0128iCRB01 heterozygote CRISPR corrected isogenic clone 02 and iso02LUMC0128iCRB01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Retinitis pigmentosa

  4109. LUMCi058-A (LUMCi231KLHL03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4110. LUMCi058-A-1 (Iso35LUMCi231KLHL03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4111. LUMCi059-A (LUMCi232KLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4112. LUMCi059-A-1 (Iso71LUMCi232KLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  4113. LUMCi062-A (LUMC0322iFOPA-03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Single ventricle defect

    Disease:

    Congenital abnormality

  4114. LUMCi062-B (LUMC0322iFOPA-05)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Single ventricle defect

    Disease:

    Congenital abnormality

  4115. LUMCi062-C (LUMC0322iFOPA-06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Single ventricle defect

    Disease:

    Congenital abnormality

  4116. LUMCi063-A (LUMC0214iAPOL)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Chronic kidney disease

  4117. LUMCi064-A (LUMC0216iAPOL)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Chronic kidney disease

  4118. LUMCi064-A-1 (ISO1LUMC0216iAPOL05)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Chronic kidney disease

  4119. LUMCi064-A-2 (ISO3LUMC0216iAPOL05)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Chronic kidney disease

  4120. LVPEIi001-A (hiPSC-F2-3F1, LVIP01-NC-F2-1 and F2-4F)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Normal (average)

  4121. LVPEIi001-B (LVIP02-NC-F2-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Normal (average)

  4122. LVPEIi002-A (LVIP02-RB-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Retinoblastoma

  4123. RUCDRi002-A-63 (LVIP05-RB1-CS1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Retinoblastoma

  4124. RUCDRi002-A-64 (LVIP05-RB1-CS2)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Retinoblastoma

  4125. RUCDRi002-A-65 (LVIP05-RB1-CS3)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Retinoblastoma

  4126. LVPEIi004-A (LVIP02-LC2-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Leber congenital amaurosis 2

  4127. LVPEIi005-A (LVIP02-LC2-2)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Leber congenital amaurosis 2

  4128. LVPEIi006-A (LVIP02-LC12-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Leber congenital amaurosis 12

  4129. LVPEIi006-B (LVIP04-LC12-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Leber congenital amaurosis 12

  4130. 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

  4131. LVPEIi007-B (LVIP04-SD1-1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Stargardt disease

  4132. LVPEIi008-A (LVIP02-SD1-2)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Stargardt disease

  4133. LVPEIi008-B (LVIP04-SD1-2)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Stargardt disease

  4134. LZUSHi001-A (ips98)

    China Lanzhou University Second Hospital (LZUSH)
    Disease:

    Generalized epilepsy

  4135. LZUSHi002-A

    China Lanzhou University Second Hospital (LZUSH)
    Disease:

    Madd

  4136. LZUSHi003-A (DMD-27-delG)

    China Lanzhou University Second Hospital (LZUSH)
    Disease:

    Duchenne muscular dystrophy

  4137. MCRIi001-A (PB001)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4138. MCRIi001-A-1 (PB001-OI26)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Osteogenesis imperfecta

  4139. MCRIi001-A-2 (MCRIi001-A-SOX9tdTom and PB001-SOX9tdTom)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4140. UCSFi001-A-1M (iN-SRCAP-R2444-3)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Floating-harbor syndrome

  4141. UCSFi001-A-1N (iN-SRCAP-R2444-5)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Floating-harbor syndrome

  4142. MCRIi002-A (PB002)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4143. MCRIi003-A (PB003)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4144. MCRIi004-A (PB004)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4145. MCRIi005-A (PB005)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4146. MCRIi006-A (PB006)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4147. MCRIi007-A (PB007)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4148. MCRIi008-A (PB008)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4149. MCRIi009-A (PB009)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4150. MCRIi010-A (PB010)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4151. MCRIi019-A (1502)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4152. MCRIi025-A (CANVAS1-2)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4153. MCRIi025-B (CANVAS1-2 Het GC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4154. MCRIi026-A (CANVAS3-2)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4155. MCRIi026-B (CANVAS3-2 Het GC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4156. MCRIi027-A (CANVAS4-6)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4157. MCRIi027-B (CANVAS4-6 Het GC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  4158. MCRIi029-A (808 iPSC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4159. 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

  4160. 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

  4161. MCRIi030-A (522 iPSC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4162. MCRIi031-A (468 iPSC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4163. 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

  4164. 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

  4165. MCRIi032-A (SCT 3010 iPSC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4166. MCRIi033-A (SCT 7002 iPSC)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal (average)

  4167. MCRIi035-A (MCRIi-TC160154-UC-cl2)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4168. MCRIi035-B (MCRIi-TC160154-UC-cl5)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4169. 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

  4170. 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

  4171. MCRIi035-C (MCRIi-TC160154-UC-cl6)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4172. MCRIi036-A (MCRIi-TC110367-UC-cl4)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4173. MCRIi036-B (MCRIi-TC110367-UC-cl5)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4174. 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

  4175. MCRIi036-C (MCRIi-TC110367-UC-cl6)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  4176. HMGUi001-A-22 (NCS1-KO Clone 19)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4177. MDCi007-A (8993-A12)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  4178. MDCi008-A (8993-B12)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  4179. MDCi009-A (8993-C11)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  4180. MDCi010-A (8993-D7)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  4181. MDCi011-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4182. MDCi011-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4183. MDCi012-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4184. MDCi012-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4185. MDCi013-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4186. MDCi013-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4187. MDCi014-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4188. MDCi014-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  4189. WTSIi018-B-18 (Kolf 2.1 J (TARDBP M337V WT/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4190. WTSIi018-B-21 (Kolf 2.1 J (TARDBP M337V SNV/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4191. WTSIi018-B-22 (Kolf 2.1 J (TARDBP Q331K WT/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4192. WTSIi018-B-23 (Kolf 2.1 J (TARDBP Q331K SNV/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4193. WTSIi018-B-24 (Kolf 2.1 J (FUS R495X WT/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4194. WTSIi018-B-25 (Kolf 2.1 J (FUS R495X SNV/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4195. WTSIi018-B-26 (Kolf 2.1 J (FUS R521H WT/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4196. WTSIi018-B-27 (Kolf 2.1 J (FUS R521H SNV/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  4197. MDCi233-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Limb-girdle muscular dystrophy type 2b

  4198. MDCi233-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Limb-girdle muscular dystrophy type 2b

  4199. MDCi237-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Maternally-inherited leigh syndrome

  4200. MDCi237-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Maternally-inherited leigh syndrome

  4201. MDCi238-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Maternally-inherited leigh syndrome

  4202. MDCi239-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Narp syndrome

  4203. METUi002-A

    Turkey Middle East Technical University (METU)

  4204. MHHi001-A (hHSC_Iso4_ADCF_SeViPS2 (Phönix))

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4205. MHHi001-A-6 (NRF2_A_Phönix-iPSC clone12)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4206. MHHi001-A-7 (NRF2_A_Phönix-iPSC clone19)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4207. MHHi001-A-20 (cyclinB1-eGFP hiPSCs)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4208. MHHi002-A (CF(1)iPS5)

    Germany Hannover Medical School (MHH)
    Disease:

    Cystic fibrosis

  4209. MHHi003-A (CF(15)iPS10)

    Germany Hannover Medical School (MHH)
    Disease:

    Cystic fibrosis

  4210. MHHi004-A (CF(16)iPS1)

    Germany Hannover Medical School (MHH)
    Disease:

    Cystic fibrosis

  4211. MHHi005-A (CF(17)iPS6)

    Germany Hannover Medical School (MHH)
    Disease:

    Cystic fibrosis

  4212. MHHi006-A (HSC1285_T-iPS2)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4213. MHHi015-A (hCD34iPSC16)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4214. MHHi015-B (hCD34iPSC11)

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  4215. MHHi029-A (F01 #20)

    Germany Hannover Medical School (MHH)

  4216. MHHi033-A (237_2020_01)

    Germany Hannover Medical School (MHH)
    Disease:

    Heritable pulmonary arterial hypertension

  4217. MHHi034-A (291_2020_01)

    Germany Hannover Medical School (MHH)
    Disease:

    Heritable pulmonary arterial hypertension

  4218. MHHi035-A (298_21_01)

    Germany Hannover Medical School (MHH)
    Disease:

    Heritable pulmonary arterial hypertension

  4219. MHHi036-A

    Germany Hannover Medical School (MHH)
    Disease:

    Heritable pulmonary arterial hypertension

  4220. MHHi037-A (207-21-01)

    Germany Hannover Medical School (MHH)
    Disease:

    Heritable pulmonary arterial hypertension

  4221. MHRCCGi001-A (P1SH)

    Russia Laboratory Clinical Genetics (MHRCCG)
    Disease:

    Schizophrenia

  4222. MHRCCGi004-A (A1SH)

    Russia Laboratory Clinical Genetics (MHRCCG)
    Disease:

    Normal (average)

  4223. MHRCCGi005-A (A2SH)

    Russia Laboratory Clinical Genetics (MHRCCG)
    Disease:

    Normal (average)

  4224. 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)

  4225. 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)

  4226. 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:

    Attention deficit hyperactivity disorder

  4227. 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:

    Attention deficit hyperactivity disorder

  4228. MILi001-A (K10 and hFF-iPSCs)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4229. MILi001-B (F5)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4230. MILi001-C (F10)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal (average)

  4231. MIPTi001-A (NAA)

    Russia Moscow Institute of Physics and Technology (MIPT)
    Disease:

    X-linked adrenoleukodystrophy

  4232. MIPTi002-A

    Russia Moscow Institute of Physics and Technology (MIPT)
    Disease:

    Hyperparathyroidism

  4233. MLi002-A (iEBS)

    Slovenia Faculty of Medicine University of Ljubljana (ML)
    Disease:

    Epidermolysis bullosa simplex

  4234. MLi003-A (iWT)

    United Kingdom Faculty of Medicine University of Ljubljana (ML)
    Disease:

    Normal (average)

  4235. MLi004-A (iMS)

    Slovenia Faculty of Medicine University of Ljubljana (ML)
    Disease:

    Epidermolysis bullosa dystrophica, autosomal recessive

  4236. MLi005-A (iDDEB)

    Slovenia Faculty of Medicine University of Ljubljana (ML)
    Disease:

    Epidermolysis bullosa dystrophica

  4237. MLUi001-M

    Germany Medical Faculty of the Martin Luther University Halle-Wittenberg (MLU)
    Disease:

    Schizophrenia

  4238. MLUi002-G

    Germany Medical Faculty of the Martin Luther University Halle-Wittenberg (MLU)
    Disease:

    Schizophrenia

  4239. MLUi007-J

    Germany Medical Faculty of the Martin Luther University Halle-Wittenberg (MLU)
    Disease:

    Alzheimer disease

  4240. MMCi001-A (MMC-iPSC-052B-02)

    Taiwan Mackay Medical College (MMC)
    Disease:

    Deafness, autosomal recessive 1a

  4241. MMCi002-A (MMC-iPSC-002-A)

    Taiwan Mackay Medical College (MMC)
    Disease:

    Hearing loss

  4242. MNDi001-A (MND-Nek1-P001)

    Germany Institut für Anatomie und Zellbiologie, Universität Ulm (MND)
    Disease:

    Amyotrophic lateral sclerosis

  4243. MNDi002-A (MND-Nek1-P002)

    Germany Institut für Anatomie und Zellbiologie, Universität Ulm (MND)
    Disease:

    Amyotrophic lateral sclerosis

  4244. MNDi003-A (MND-Nek1-P003)

    Germany Institut für Anatomie und Zellbiologie, Universität Ulm (MND)
    Disease:

    Amyotrophic lateral sclerosis

  4245. MNDi004-A (MND-Nek1-P004)

    Germany Institut für Anatomie und Zellbiologie, Universität Ulm (MND)
    Disease:

    Amyotrophic lateral sclerosis

  4246. MNDi005-A (MND-Nek1/C9-P001)

    Germany Institut für Anatomie und Zellbiologie, Universität Ulm (MND)
    Disease:

    Amyotrophic lateral sclerosis

  4247. MNZTASi001-A (MS_0004, 2125-2 and TOB-02125)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Primary progressive multiple sclerosis

  4248. MNZTASi002-A (MS_0001.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4249. MNZTASi003-A (MS_0002)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4250. MNZTASi004-A (MS_0003)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4251. MNZTASi005-A (MS_0006)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4252. MNZTASi006-A (MS_0005, TOB-02161 and 2161-4)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Primary progressive multiple sclerosis

  4253. MNZTASi007-A (MS_0007)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4254. MNZTASi009-A (MS_0009.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4255. MNZTASi009-B (MS_0009.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4256. MNZTASi010-A (MS_0010)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4257. MNZTASi014-A (MS_0014)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4258. MNZTASi015-A (MS_0015.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4259. MNZTASi015-B (MS_0015.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4260. MNZTASi015-C (MS_0015.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4261. MNZTASi016-A (MS_0016)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4262. MNZTASi017-A (MS_0017)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4263. MNZTASi018-A (MS_0018)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4264. MNZTASi019-A (MS_0019)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4265. MNZTASi020-A (MS_0020.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4266. MNZTASi020-B (MS_0020.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4267. MNZTASi021-A (MS_0021)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4268. MNZTASi022-A (MS_0022)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4269. MNZTASi029-A (MS_0029.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4270. MNZTASi029-B (MS_0029.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4271. MNZTASi029-C (MS_0029.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4272. MNZTASi030-A (MS_0030.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4273. MNZTASi030-B (MS_0030.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4274. MNZTASi030-C (MS_0030.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4275. MNZTASi031-A (MS_0031.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Secondary progressive multiple sclerosis

  4276. MNZTASi031-B (MS_0031.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Secondary progressive multiple sclerosis

  4277. MNZTASi031-C (MS_0031.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Secondary progressive multiple sclerosis

  4278. MNZTASi032-A (MS_0032.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4279. MNZTASi032-B (MS_0032.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4280. MNZTASi032-C (MS_0032.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4281. MNZTASi033-A (MS_0033.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4282. MNZTASi033-B (MS_0033.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4283. MNZTASi033-C (MS_0033.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Relapsing-remitting multiple sclerosis

  4284. MNZTASi034-A (MS_0034.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4285. MNZTASi034-B (MS_0034.2)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4286. MNZTASi034-C (MS_0034.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  4287. MONUi001-A (86200001.1)

    Australia Monash University (MONU)
    Disease:

    Autism spectrum disorder

  4288. MONUi001-B (86200001.2)

    Australia Monash University (MONU)
    Disease:

    Autism spectrum disorder

  4289. MONUi001-C (86200001.4)

    Australia Monash University (MONU)
    Disease:

    Autism spectrum disorder

  4290. MONUi002-A (86202443.3)

    Australia Monash University (MONU)
    Disease:

    Autism spectrum disorder

  4291. MONUi002-B (86202443.5)

    Australia Monash University (MONU)
    Disease:

    Autism spectrum disorder

  4292. MONUi002-C (86202443.6)

    Australia Monash University (MONU)
    Disease:

    Autism spectrum disorder

  4293. MONUi003-A (86203213.1)

    Australia Monash University (MONU)
    Disease:

    Autism spectrum disorder

  4294. MONUi003-B (86203213.2)

    Australia Monash University (MONU)
    Disease:

    Autism spectrum disorder

  4295. MONUi003-C (86203213.4)

    Australia Monash University (MONU)
    Disease:

    Autism spectrum disorder

  4296. MPIi001-A

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Normal (average)

  4297. MPIi002-A (T4 and L1-1Mut)

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Obsolete_parkinson's disease

  4298. MPIi003-A (IM2 and L2-2Mut)

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Obsolete_parkinson's disease

  4299. MPIi003-A-1 (IM2GC and L2-2GC)

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Obsolete_parkinson's disease

  4300. MPIi005-A (SF2.1 and wt1)

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Normal (average)

  4301. MPIPi057-A (UL1)

    Germany Max Planck Institute of Psychiatry (MPIP)
    Disease:

    Progressive myoclonic epilepsy type 1

  4302. MPIPi058-A (UL4)

    Germany Max Planck Institute of Psychiatry (MPIP)
    Disease:

    Progressive myoclonic epilepsy type 1

  4303. MRIi001-A (C6)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4304. MRIi001-A-1 (C6-AAVS1-iCasRx)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4305. MRIi003-A (HK)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4306. MRIi003-A-1 (MYH10+/-)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4307. MRIi003-A-2 (MYH10-/-)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4308. MRIi003-A-3 (TRPM4+/-)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4309. MRIi003-A-4 (TRPM4-/-)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4310. MRIi003-A-5 (AAVS1-CAG-VSFP-hetero)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4311. MRIi003-A-6 (AAVS1-CAG-VSFP-homo)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4312. MRIi003-A-7 (HK-AAVS1-iCasRx)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4313. MRIi003-A-8 (HK-AAVS1-CAG-eGFP-homo)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4314. MRIi003-A-9 (HK-AAVS1-CAG-FRT-stop-FRT-mKate2-hetero)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4315. MRIi003-A-10 (AAVS-CAG-DTPA-R heterozygous)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4316. MRIi003-A-11 (AAVS-CAG-DTPA-R homozygous)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  4317. MRIi005-A

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Long qt syndrome 1

  4318. MRIi010-A (DCM)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Dilated cardiomyopathy 1g

  4319. MRIi016-A (Shox2.1)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Atrial fibrillation

  4320. MRIi017-A (TRPM4)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Brugada syndrome

  4321. MRIi018-A (HLHS_375)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Hypoplastic left heart syndrome

  4322. MRIi024-A (Shox2.2)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Atrial fibrillation

  4323. MRIi025-A (Noonan 3a)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Noonan syndrome

  4324. MRIi026-A (Noonan 3d)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Noonan syndrome

  4325. MRIi027-A (DMD 01)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Duchenne muscular dystrophy

  4326. MRIi028-A (PPC-4)

    Germany Klinikum rechts der Isar (MRI)

  4327. MRIi030-A (LVNC1)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Left ventricular noncompaction cardiomyopathy

  4328. MRIi031-A (LVNC2)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Left ventricular noncompaction cardiomyopathy

  4329. MRIi032-A (LVNC3)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Left ventricular noncompaction cardiomyopathy

  4330. MSKi002-A (C27 and iPS-27)

    United States Memorial Sloan Kettering Cancer Center (MSK)
    Disease:

    Normal (average)

  4331. MUi010-A (MYH9)

    Thailand Mahidol University (MU)
    Disease:

    Myh9-related syndromic thrombocytopenia

  4332. MUi015-A (RB1)

    Thailand Mahidol University (MU)
    Disease:

    Retinoblastoma

  4333. MUi026-A (MU012.C4)

    Thailand Mahidol University (MU)
    Disease:

    Autosomal dominant polycystic kidney disease

  4334. MUi027-A (MU013.C2)

    Thailand Mahidol University (MU)

  4335. MUi028-A

    Thailand Mahidol University (MU)
    Disease:

    Normal (average)

  4336. MUi030-A (Gaucher iPSC2)

    Thailand Mahidol University (MU)
    Disease:

    Gaucher disease type 3

  4337. MUi031-A (Gaucher iPSC3)

    Thailand Mahidol University (MU)
    Disease:

    Gaucher disease type 3

  4338. MUi032-A

    Thailand Mahidol University (MU)
    Disease:

    Choroideremia

  4339. MUi033-A (MU020 and homoHbE iPSC)

    Thailand Mahidol University (MU)
    Disease:

    Normal (average)

  4340. MUi034-A (homoHbCS iPSC and MU018)

    Thailand Mahidol University (MU)
    Disease:

    Alpha thalassemia spectrum

  4341. MUi038-A (EYS mutation)

    Thailand Mahidol University (MU)
    Disease:

    Retinitis pigmentosa

  4342. MUi040-A

    Thailand Mahidol University (MU)
    Disease:

    Amyloidosis

  4343. MUBi002-A (CF 001)

    Poland Medical University of Bialystok (MUB)
    Disease:

    Cystic fibrosis

  4344. MUBi005-A (iPSC_COPD)

    Poland Medical University of Bialystok (MUB)
    Disease:

    Chronic obstructive pulmonary disease

  4345. MUNIi001-A (DMD02)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  4346. MUNIi002-A (MDMD02)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  4347. MUNIi003-A (DMD03)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  4348. MUNIi004-A (DMD04)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  4349. MUNIi005-A (fAD1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer disease 3

  4350. MUNIi006-A (fAD2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer disease 3

  4351. MUNIi007-A (fAD3 and ADF81)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer disease 4

  4352. MUNIi008-A (fWT1, WTM52, fHC1 and fCTRL1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4353. MUNIi009-A (fWT2, WTF50, fHC2 and fCTRL2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4354. MUNIi010-A (WTF80, fHC3, fWT3 and fCTRL3)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4355. MUNIi011-A (BAD1 and sAD1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer's disease

  4356. MUNIi012-A (BAD2 and sAD2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer's disease

  4357. MUNIi013-A (BAD4 and sAD3)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer's disease

  4358. MUNIi014-A (sHC1, BHC2 and sCTRL1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4359. MUNIi015-A (sHC2, BHC1 and sCTRL2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4360. MUNIi016-A (sHC3, BHC3 and sCTRL3)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4361. MUNIi017-A (BWT3)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4362. MUNIi018-A (HUVEC-iPSC)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4363. MUNIi018-B (HUVEC-hiPSC-macroH2A1.1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4364. MUNIi018-C (HUVEC-hiPSC-macroH2A1.2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4365. MUNIi018-D (mHU-C)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4366. MUNIi019-A (NBS-M and NBS)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Nijmegen breakage syndrome

  4367. MUNIi020-A (sHC5)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4368. MUNIi021-A (sAD5)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer's disease

  4369. MUNIi022-A (PKP2 and PKP2_AKAP9)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  4370. MUNIi023-A (mUC-K)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4371. MUNIi024-A (PB2C1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4372. MUNIi025-A (mLAM-A)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4373. MUNIi025-B (mLAM-D)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  4374. MURAi001-A (TET1mutationC18)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)

  4375. MURAi002-A (-4bp/HbE C11)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Hemoglobin e-beta-thalassemia syndrome

  4376. MURAi003-A (HoHLA, Homozygous-HLA and HoHLA C3)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Normal (average)

  4377. MURAi006-A (FL23C9)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Hemoglobin e-beta-thalassemia syndrome

  4378. MUSCSDi001-A (iPSK3)

    United States Steve's Duncan Lab (MUSCSD)
    Disease:

    Normal (average)

  4379. MUSCSDi001-A-1 (PCCB ∆14/∆29)

    United States Steve's Duncan Lab (MUSCSD)
    Disease:

    Propionic acidemia

  4380. MUSCSDi001-A-2 (PCCB ∆19/∆481)

    United States Steve's Duncan Lab (MUSCSD)
    Disease:

    Propionic acidemia

  4381. MUSIi001-A (SFiPSC01)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4382. MUSIi001-A-1 (B2M-KO-SFiPSC5 and HLA-I-null SFiPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4383. MUSIi001-A-2 (HLA-I/II-null SFiPSCs and B2M-/-/CIITA-/- SFiPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4384. MUSIi001-A-3 (TIGIT-KO-SFiPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4385. MUSIi004-A

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Spinocerebellar ataxia type 3

  4386. MUSIi005-A (SUiPSC02)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4387. MUSIi006-A (SKiPSC02)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4388. MUSIi009-A (HDF-iPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4389. MUSIi011-A (STiPSC01.1)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4390. MUSIi011-B (STiPSC01.8)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4391. MUSIi013-A (CBNK-iPSC)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4392. MUSIi013-A-2 (CAR-TIM3 iPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4393. MUSIi016-A (TyO)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4394. MUSIi017-A (Oneg)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4395. MUSIi019-A (SLC4A1-21-C1)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Distal renal tubular acidosis

  4396. MUSIi023-A (hmziPSC and Homozygous HLA iPSC)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  4397. NCAi001-A

    Netherlands Ncardia B.V. (NCA)
    Disease:

    Normal (average)

  4398. NCBSi003-A (Park14-R741Q-2022)

    India National Center for Biological Sciences (NCBS)
    Disease:

    Autosomal recessive parkinson disease 14

  4399. NCBSi004-A (Park14-control-2022)

    India National Center for Biological Sciences (NCBS)
    Disease:

    Normal (average)

  4400. NCCSEDi001-A

    China National Chengdu Center for Safety Evaluation of Drugs (NCCSED)
    Disease:

    Normal (average)

  4401. NCCSEDi001-A-1

    China National Chengdu Center for Safety Evaluation of Drugs (NCCSED)
    Disease:

    Intellectual developmental disorder 61

  4402. NCHi001-A (LCL-iPSC4802)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Congenital heart disease

  4403. NCHi003-A (NCH005)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Pulmonary valve atresia with intact ventricular septum

  4404. NCHi004-A (NCH140)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Down syndrome

  4405. NCHi006-A (NCH023)

    United States Nationwide Children's Hospital (NCH)

  4406. NCHi009-A (NCH78)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Hypoplastic left heart syndrome

  4407. NCHi010-A (NCH141)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Down syndrome

  4408. NCHi011-A (NCH092)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Alagille syndrome

  4409. NCHi012-A (NCH089)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Alagille syndrome

  4410. NCHi013-A (NCH17)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Pulmonary valve atresia with intact ventricular septum

  4411. NCHi014-A (NCH3-N1HET)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Normal (average)

  4412. NCHi015-A (NCH178)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Type i truncus arteriosus

  4413. NCHi016-A (NCH012)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Pulmonary atresia-intact ventricular septum syndrome

  4414. NCHi020-A (S63del hiPSCs)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Charcot-marie-tooth disease type 1b

  4415. NCHi021-A (R98C hiPSCs)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Charcot-marie-tooth disease type 1b

  4416. NCHi023-A (NCH217)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Nemaline myopathy

  4417. NCHi024-A (NCH27)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Bicuspid aortic valve

  4418. NCHi025-A

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Pulmonary stenosis

  4419. NCHi026-A (iPSC486AB)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Duchenne muscular dystrophy

  4420. NCHi027-A

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Cloaca

  4421. NCHi028-A

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Prune belly syndrome

  4422. NCKDi006-A (NCKD-iPS-FSGS-TRPC6-006)

    China National Center of Kidney Diseases (NCKD)
    Disease:

    Focal segmental glomerulosclerosis

  4423. NCKUi001-A (human amniotic fluid stem cells derived iPSC and hAFSC-iPSC)

    Taiwan National Cheng Kung University (NCKU)
    Disease:

    Normal (average)

  4424. NCSi001-A (NCS065)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Alzheimer's disease

  4425. NCSi002-A (NCS066)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Normal (average)

  4426. NCSi003-A (NCS067)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Normal (average)

  4427. NCSi004-A (NCS068)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Normal (average)

  4428. NCSi005-A (NCS069)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Alzheimer's disease

  4429. NCSi006-A (NCS070)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Normal (average)

  4430. NCSi007-A (NCS071)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Alzheimer's disease

  4431. NEIi001-A (iPSC-F34)

    United States National institutes of Health (NEI)
    Disease:

    Opa1-related optic atrophy with or without extraocular features

  4432. NEIi002-A (iPSC-F35)

    United States National institutes of Health (NEI)
    Disease:

    Opa1-related optic atrophy with or without extraocular features

  4433. NEIi003-A (iPSC-F36)

    United States National institutes of Health (NEI)
    Disease:

    Opa1-related optic atrophy with or without extraocular features

  4434. NEIi004-A (iPSC-F41)

    United States National institutes of Health (NEI)
    Disease:

    Opa1-related optic atrophy with or without extraocular features

  4435. NENCKIi001-A (MPAN-3.1)

    Poland Nencki Institute of Experimental Biology PAS (NENCKI)
    Disease:

    Mitochondrial membrane protein-associated neurodegeneration

  4436. NENCKIi002-A (MPAN-9.3)

    Poland Nencki Institute of Experimental Biology PAS (NENCKI)
    Disease:

    Mitochondrial membrane protein-associated neurodegeneration

  4437. NENCKIi003-A (MPAN-18.1)

    Poland Nencki Institute of Experimental Biology PAS (NENCKI)
    Disease:

    Mitochondrial membrane protein-associated neurodegeneration

  4438. NENCKIi004-A (MPAN-22.3)

    Poland Nencki Institute of Experimental Biology PAS (NENCKI)
    Disease:

    Mitochondrial membrane protein-associated neurodegeneration

  4439. NERCi001-A

    China National Engineering and Research Center of Human Stem Cell (NERC)
    Disease:

    Dyskeratosis congenita

  4440. NFHHMUi001-A

    China Department of Neurosurgery of The First Affiliated Hospital of Harbin Medical University (NFHHMU)
    Disease:

    Cerebral cavernous malformation

  4441. NHGRIi001-A (iPSC-1 and FISAL04_Sia80)

    United States National Human Genome Research Institute (NHGRI)

  4442. NHGRIi002-A (iPSC-2 and CDG.1121_Sia74)

    United States National Human Genome Research Institute (NHGRI)

  4443. NHLBIi001-A (MS19-ES-D)

    United States NHLBI iPSC Core (NHLBI)
    Disease:

    Normal (average)

  4444. NHLBIi001-B (MS19-ES-H)

    United States NHLBI iPSC Core (NHLBI)
    Disease:

    Normal (average)

  4445. NHLBIi003-A (ND2.0 and mND2-0)

    United States NHLBI iPSC Core (NHLBI)
    Disease:

    Normal (average)

  4446. NHLBIi003-A-1 (ND2-tdTom1)

    United States NHLBI iPSC Core (NHLBI)
    Disease:

    Normal (average)

  4447. NHLBIi003-A-2 (ND2-tdTom4)

    United States NHLBI iPSC Core (NHLBI)
    Disease:

    Normal (average)

  4448. NIHTVBi016-A (HT876D)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  4449. NIHTVBi017-A (HT939A)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  4450. NIHTVBi018-A (HT940B)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  4451. NIHTVBi019-A (HT852)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Leukodystrophy

  4452. NIHTVBi019-A-1 (HT852-DC)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Leukodystrophy

  4453. NIHTVBi020-A (HT853)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Normal (average)

  4454. NIHTVBi021-A (HT854)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Normal (average)

  4455. NIHTVBi022-A (HT964)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Leukodystrophy

  4456. NIHTVBi024-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  4457. NIHTVBi025-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Sting-associated vasculopathy with onset in infancy

  4458. NIHTVBi026-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Sting-associated vasculopathy with onset in infancy

  4459. NIHTVBi027-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Sting-associated vasculopathy with onset in infancy

  4460. NIHTVBi028-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Lyn gene mutation

  4461. NIHTVBi029-A (HT1127A (NIHTVBi029-A))

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Cdc42

  4462. NIHTVBi030-A (HT1128A (NIHTVBi030-A))

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Cdc42 gene

  4463. NIHTVBi031-A (HT1129D)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Autoimmune interstitial lung, joint, and kidney disease

  4464. NIMHi001-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Obsolete_parkinson's disease

  4465. NIMHi002-A (BPPD02)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Parkinson disease

  4466. NIMHi003-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Parkinson disease

  4467. NIMHi004-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4468. NIMHi005-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4469. NIMHi006-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4470. NIMHi007-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4471. NIMHi008-A (NphyiALS1)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Amyotrophic lateral sclerosis

  4472. NIMHi009-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4473. NIMHi010-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4474. NIMHi011-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Congenital myasthenic syndrome

  4475. NIMHi012-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Epilepsy

  4476. NIMHi013-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Epilepsy

  4477. NIMHi014-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Epilepsy

  4478. NIMHi015-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Autosomal recessive juvenile parkinson disease 2

  4479. NIMHi016-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Phosphoglycerate kinase 1 deficiency

  4480. NIMHi017-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Biotin-responsive basal ganglia disease

  4481. NIMHi018-A (PD07)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Parkinson's disease 6

  4482. NIMHi019-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Congenital myasthenic syndrome

  4483. NIMHi020-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Mitochondrial disease

  4484. NIMHi021-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4485. NIMHi022-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Congenital myasthenic syndrome

  4486. NIMHi023-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal (average)

  4487. NIMHi026-A (MSA1)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Multiple system atrophy

  4488. NIMHi027-A (PD09)

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Early-onset parkinson's disease

  4489. NJDTHi001-A

    China Department of Cardio-Thoracic Surgery, Nanjing Drum Tower Hospital (NJDTH)
    Disease:

    Danon disease

  4490. NMIi001-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Normal (average)

  4491. TMOi001-A-5 (DISC1 Ex2 D5)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Normal (average)

  4492. TMOi001-A-6 (DISC1 Ex2 C4)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Normal (average)

  4493. NMIi002-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4494. NMIi002-B

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4495. NMIi004-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4496. NMIi005-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4497. NMIi006-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4498. NMIi006-B

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Schizophrenia

  4499. NMIi010-A

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Normal (average)

  4500. NMIi011-A (B1.4)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4501. NMIi011-B (B1.6)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4502. NMIi011-C (B1.7)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4503. NMIi011-D (B1.10)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4504. NMIi012-A (DG1)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4505. NMIi012-B (DG2)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4506. NMIi012-D (DG4)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4507. NMIi012-E (DG5)

    Germany NMI Natural and Medical Sciences Institute at the University of Tübingen (NMI)
    Disease:

    Breast carcinoma

  4508. NRIFPi001-A (WJWKYSi001-A)

    China National Research Institute for Family Planning (NRIFP)
    Disease:

    Phenylketonuria

  4509. NSi003-A (NSi-DS)

    India Stem Cell and Neurobiology Lab (NS)
    Disease:

    Down syndrome

  4510. NSi003-B (NSi-isoEu)

    India Stem Cell and Neurobiology Lab (NS)
    Disease:

    Down syndrome

  4511. NSHDMUi001-A

    China Department of Neurology of the Second Hospital of Dalian Medical University (NSHDMU)
    Disease:

    Diabetes mellitus

  4512. NTUHi002-A

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Aceruloplasminemia

  4513. NTUHi004-A

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Leigh syndrome

  4514. NTUHi005-A (IBMS-iPSC-071-01)

    Taiwan National Taiwan University Hospital (NTUH)

  4515. NTUHi006-A (NTUH-iPSC-008-1)

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Polycystic ovary syndrome

  4516. NUIGi001-A (iPSC ARO1-11)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autosomal recessive osteopetrosis

  4517. NUIGi003-A (LQT002C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4518. NUIGi003-B (LQT002C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4519. NUIGi004-A (LQT003C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4520. NUIGi005-A (LQTS004C7 and LQT004C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4521. NUIGi005-B (LQTS004C9 and LQT004C9)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4522. NUIGi005-C (LQTS004Cx and LQT004Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4523. NUIGi006-A (LQTS005C2 and LQT005C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4524. NUIGi006-B (LQTS005C4 and LQT005C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4525. NUIGi006-C (LQTS005Cx and LQT005Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4526. NUIGi007-A (LQTS006C6 and LQT006C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4527. NUIGi007-B (LQTS006C8 and LQT006C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4528. NUIGi008-A (LQTS007C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4529. NUIGi008-B (LQTS007C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4530. NUIGi008-C (LQTS007Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4531. NUIGi009-A (LQTS008C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4532. NUIGi009-B (LQTS008C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4533. NUIGi009-C (LQTS008Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4534. NUIGi010-A (LQTS009C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4535. NUIGi010-B (LQTS009C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4536. NUIGi010-C (LQTS009Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4537. NUIGi011-A (LQTS010C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4538. NUIGi011-B (LQTS010C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4539. NUIGi011-C (LQTS010Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  4540. NUIGi012-A (LQT011C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4541. NUIGi015-A (LQT014C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4542. NUIGi015-B (LQT014C9)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4543. NUIGi015-C (LQT014C12)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4544. NUIGi018-A (LQT017C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4545. NUIGi018-B (LQT017C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4546. NUIGi018-C (LQT017Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4547. NUIGi020-A (LQT019C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4548. NUIGi020-B (LQT019C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4549. NUIGi020-C (LQT019Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  4550. NUIGi022-A (ND11C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4551. NUIGi022-B (ND11C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4552. NUIGi023-A (ND12C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4553. NUIGi023-B (ND12C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4554. NUIGi024-A (CND13C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4555. NUIGi024-B (CND13C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4556. NUIGi025-A (ND14C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4557. NUIGi025-B (ND14C9)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism

  4558. NUIGi026-A (CND15C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4559. NUIGi026-B (CND15C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4560. NUIGi027-A (RP001C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Retinitis pigmentosa

  4561. NUIGi028-A (RP002C12)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Retinitis pigmentosa

  4562. NUIGi029-A (RP003C12)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Retinitis pigmentosa

  4563. NUIGi033-A (ASD012-Q)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism spectrum disorder

  4564. NUIGi034-A (ASDC012-AI)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4565. NUIGi035-A (02V-AD)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4566. NUIGi036-A (03V-D)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4567. NUIGi037-A (05C-J)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4568. NUIGi038-A (LQTH002C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4569. NUIGi038-B (LQTH002Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4570. NUIGi038-B-1 (CR.LQTH002Cx-A17)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4571. NUIGi038-B-2 (CR.LQTH002Cx-A21)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4572. NUIGi038-B-3 (CR.LQTH002Cx-3A15)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4573. NUIGi038-B-4 (CR.LQTH002Cx-3A18)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  4574. NUIGi038-C (LQTH002C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4575. NUIGi039-A (ND1C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism spectrum disorder

  4576. NUIGi039-B (ND1C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism spectrum disorder

  4577. NUIGi040-A (CND1C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4578. NUIGi040-B (CND1C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4579. NUIGi041-A (ND3C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism spectrum disorder

  4580. NUIGi041-B (ND3C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism spectrum disorder

  4581. NUIGi042-A (CND3C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4582. NUIGi042-B (CND3C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4583. NUIGi043-A (ALS52C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4584. NUIGi043-B (ALS52C9)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4585. NUIGi043-C (ALS52C10)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4586. NUIGi044-A (ALS69C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4587. NUIGi044-B (ALS69C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4588. NUIGi044-C (ALS69C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4589. NUIGi045-A (ND2C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Autism spectrum disorder

  4590. NUIGi046-A (LQTH001C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4591. NUIGi046-B (LQTH001C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4592. NUIGi046-C (LQTH001C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4593. NUIGi047-A (LQTH003C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4594. NUIGi047-B (LQTH003C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4595. NUIGi047-C (LQTH003Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4596. NUIGi048-A (ALSH84C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4597. NUIGi048-B (ALSH84C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4598. NUIGi048-C (ALSH84C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4599. NUIGi049-A (ALSH47C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4600. NUIGi049-B (ALSH47C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4601. NUIGi049-C (ALSH47C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4602. NUIGi050-A (ALS53C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4603. NUIGi050-B (ALS53C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4604. NUIGi050-C (ALS53C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4605. NUIGi051-A (ALS57C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4606. NUIGi051-B (ALS57C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4607. NUIGi051-C (ALS57C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4608. NUIGi052-A

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Non-specific early-onset epileptic encephalopathy

  4609. NUIGi052-B

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Non-specific early-onset epileptic encephalopathy

  4610. NUIGi052-C

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Non-specific early-onset epileptic encephalopathy

  4611. NUIGi055-A (iPSC C1-15)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4612. NUIGi055-B (iPSC C1-16)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4613. NUIGi055-C (iPSC C1-17)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4614. NUIGi059-A (EP2001 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Epileptic encephalopathy

  4615. NUIGi059-B (EP2001 C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Epileptic encephalopathy

  4616. NUIGi059-C (EP2001 C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Epileptic encephalopathy

  4617. NUIGi060-A (EP2C001 C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4618. NUIGi060-B (EP2C001 C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4619. NUIGi060-C (EP2C001 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4620. NUIGi063-A (EP2003 C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Kcnq2-related developmental and epileptic encephalopathy

  4621. NUIGi063-B (EP2003 C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Kcnq2-related developmental and epileptic encephalopathy

  4622. NUIGi063-C (EP2003 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Kcnq2-related developmental and epileptic encephalopathy

  4623. NUIGi064-A (EP2C003 C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4624. NUIGi064-B (EP2C003 C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4625. NUIGi064-C (EP2C003 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  4626. NUMNi001-A

    Japan Department of Nephrology, Nagoya University Hospital (NUMN)
    Disease:

    Normal (average)

  4627. NUMNi002-A

    Japan Department of Nephrology, Nagoya University Hospital (NUMN)

  4628. NUMNi003-A

    Japan Department of Nephrology, Nagoya University Hospital (NUMN)
    Disease:

    Autosomal dominant polycystic kidney disease

  4629. NYSCFi001-A (AL0002-01-MR-131)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4630. NYSCFi001-B (AL0002-01-MR-132)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4631. NYSCFi001-C (AL0002-01-SV-008)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4632. NYSCFi001-D (AL0002-01-SV-010)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4633. NYSCFi002-A (AL0004-01-SV-002)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4634. NYSCFi002-B (AL0004-01-SV-008)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal (average)

  4635. NYSCFi003-A (CO0002-01-SV-003)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Alzheimer's disease

  4636. OFi001-A (ASD011-A)

    South Korea OrganFactory (OF)
    Disease:

    Autism spectrum disorder

  4637. OFi002-A (OFi015-A)

    South Korea OrganFactory (OF)
    Disease:

    Autism spectrum disorder

  4638. OGIi001-A

    United States Ocular Genomics Institute at Mass Eye and Ear Hospital (OGI)
    Disease:

    Normal (average)

  4639. ORIONi001-A (iALS-1)

    Slovakia Biomedical center Martin, Jessenius Faculty of Medicine in Martin, COMENIUS UNIVERSITY IN BRATISLAVA (ORION)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4640. ORIONi002-A (iALS-2)

    Slovakia Biomedical center Martin, Jessenius Faculty of Medicine in Martin, COMENIUS UNIVERSITY IN BRATISLAVA (ORION)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  4641. ORIONi003-A

    Slovakia Biomedical center Martin, Jessenius Faculty of Medicine in Martin, COMENIUS UNIVERSITY IN BRATISLAVA (ORION)
    Disease:

    Duchenne muscular dystrophy

  4642. 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

  4643. OSRi001-A (PD-OPA1-A495V#72)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Parkinson disease

  4644. OSRi004-A (ND#37)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Normal (average)

  4645. OSRi005-A (ND#68)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Normal (average)

  4646. OSRi009-A (SGS_D868N)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Schinzel-giedion midface-retraction syndrome

  4647. OSRi009-A-1 (SGS_D868D)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Schinzel-giedion midface-retraction syndrome

  4648. OSRi010-A (SGS_I871T)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Schinzel-giedion midface-retraction syndrome

  4649. OSRi010-A-1 (SGS_I871I)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Schinzel-giedion midface-retraction syndrome

  4650. OSRi011-A (4xSNCA)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Parkinsonian disorder

  4651. OSRi011-A-1 (Iso SNCA)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Parkinsonian disorder

  4652. OSRi013-A (OSR_001#10)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Multiple sclerosis

  4653. OSRi014-A (OSR_002#1)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Multiple sclerosis

  4654. OSRi015-A (OSR_003#56)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Multiple sclerosis

  4655. OSRi016-A (OSR_004#30)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Multiple sclerosis

  4656. OSRi017-A (PTL6)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4657. OSRi017-A-1 (PTL6-SD10)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4658. OSRi017-A-2 (PTL6-LD3)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4659. OSRi018-A (PTS36)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4660. OSRi018-A-1 (PTS36-SD23)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4661. OSRi018-A-2 (PTS36-LD3)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Friedreich ataxia

  4662. OTATi001-A (HC4)

    United States Office of Tissues and Advanced Therapies, CBER, FDA (OTAT)
    Disease:

    Normal (average)

  4663. OTATi002-A (HC8)

    United States Office of Tissues and Advanced Therapies, CBER, FDA (OTAT)
    Disease:

    Normal (average)

  4664. PCIi001-A (PC124)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4665. PCIi003-A (PC126)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4666. PCIi004-A (PC127)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4667. PCIi005-A (PC137)

    France PHENOCELL (PCI)
    Disease:

    Danon disease

  4668. PCIi007-A (PC153)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4669. PCIi008-A (PC154)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4670. PCIi009-A (PC168)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4671. PCIi010-A (PC169)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4672. PCIi011-A (PC170)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4673. PCIi012-A (PC171)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4674. PCIi015-A (PC191)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4675. PCIi016-A (PC192)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4676. PCIi017-A (PC198)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4677. PCIi018-A (PC199)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4678. PCIi019-A (PC200)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4679. PCIi020-A (PC201)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4680. PCIi021-A (PC202)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4681. PCIi022-A (PC203)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4682. PCIi023-A (PC204)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4683. PCIi024-A (PC205)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4684. PCIi025-A (PC084)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  4685. PCIi026-A (PC085)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  4686. PCIi027-A (PC086)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  4687. PCIi029-A (PC076)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome type 1

  4688. PCIi030-A (PC078)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome type 1

  4689. PCIi031-A (PC079)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome type 1

  4690. PCIi032-A (PC087)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  4691. PCIi033-A (PCi-CAU2)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  4692. PCIi034-A (PC138)

    France PHENOCELL (PCI)
    Disease:

    Aicardi-goutieres syndrome

  4693. PCIi035-A (PC139)

    France PHENOCELL (PCI)
    Disease:

    Aicardi-goutieres syndrome

  4694. WTSIi018-B-13

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Ataxia telangiectasia syndrome

  4695. WTSIi018-B-14

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Ataxia telangiectasia syndrome

  4696. WTSIi018-B-15

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Ataxia telangiectasia syndrome

  4697. WTSIi018-B-16

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Ataxia telangiectasia syndrome

  4698. PEIi021-A (PEIi004-A)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4699. PEIi021-B (PEIi004-B)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4700. PEIi021-C (PEIi004-C)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4701. PEIi021-D (PEIi004-D)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4702. PEIi022-A (PEIi005-A)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4703. PEIi022-B (PEIi005-B)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4704. PEIi022-C (PEIi005-C)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4705. PEIi022-D (PEIi005-D)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  4706. PENNi001-A (PENN123i-SV20 and SV20)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4707. PENNi001-A-1 (SV20 ACE2KO D1)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4708. PENNi002-A (ND535 Sev1)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4709. PENNi003-A (HPAP021 Sev2)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  4710. PENNi004-A (HPAP030 Sev10)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  4711. PENNi005-A (HPAP031 Sev7)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  4712. PENNi006-A (HPAP112 Sev12)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4713. PENNi007-A (HPAP114 Sev10)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4714. PENNi008-A (HPAP135 Sev7)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  4715. PENNi009-A (HPAP149 Sev3)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  4716. PENNi010-A (HPAP155 Sev2)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  4717. PFIZi001-A (EM1-3F)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4718. RCi001-A (Thp3C-6 and RCi88)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4719. RCi001-B (RCi89 and Thp3C-9)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4720. PFIZi002-A (EM1-7M)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4721. RCi002-A (FP5C-14 and RCi92)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4722. RCi002-B (FP5C-16 and RCi93)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4723. PFIZi003-A (EM2-7M)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4724. RCi003-A (RCi115 and CIP11A-5)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Pain agnosia

  4725. RCi003-B (CIP11A-9 and RCi117)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Pain agnosia

  4726. PFIZi004-A (EM2-7F)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  4727. PFIZi009-A (RCi188)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4728. PFIZi010-A (FB65c7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  4729. PFIZi010-B (FB65c16)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  4730. PFIZi010-C (FB65c20)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  4731. PFIZi011-A (RCi199 and FB67c2)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  4732. PFIZi012-A (FB66c17 and RCi198)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  4733. PFIZi013-A (RCi215 and RCFB59 C9)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Amyotrophic lateral sclerosis

  4734. PFIZi014-A (OD002-s7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4735. PFIZi015-A (OD003-s5)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4736. PFIZi016-A (OD005-s9)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4737. PFIZi017-A (BC142c7 and RCi209)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4738. PFIZi018-A (BC143c8 and RCi207)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4739. PFIZi019-A (RCi202 and BC145c6)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4740. PFIZi021-A (OD001-s7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  4741. PFIZi022-A (B219c2)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epileptic encephalopathy

  4742. PFIZi023-A (B217c8)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Bilateral frontoparietal polymicrogyria

  4743. PFIZi024-A (B218c6)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epilepsy

  4744. PFIZi025-A (B220c16)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epilepsy

  4745. PFIZi027-A (B221c13)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Lissencephaly

  4746. PFIZi028-A (B212c7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Neurodevelopmental disorder

  4747. PFIZi029-A (B222c4)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Myoclonic epilepsy

  4748. PFIZi030-A (B216c13)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Acromesomelic dysplasia

  4749. PFIZi031-A (B213c1)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epileptic encephalopathy

  4750. PFIZi032-A (B214c8)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Tuberous sclerosis

  4751. PGNMi001-A (AG08C5)

    France Institut NeuroMyoGene - Pathophysiology and Genetics of Neuron and Muscle (INMG-PGNM) (PGNM)
    Disease:

    Normal (average)

  4752. PHAi003-A (PIDi003-A)

    Sweden Pan-Hammarström laboratory (PHA)
    Disease:

    Primary immunodeficiency

  4753. PHAi003-B (PIDi003-B)

    Sweden Pan-Hammarström laboratory (PHA)
    Disease:

    Primary immunodeficiency

  4754. PMUi001-A (Alice and BMACA-CT2-A)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal (average)

  4755. PMUi001-B (Betty and BMACA-CT2-B)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal (average)

  4756. PMUi001-C (Chantal and BMACA-CT2-C)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal (average)

  4757. PMUi002-A (Cornelius and UCB144-CT2-C)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal (average)

  4758. PMUi002-A-1 (UCB144-CT2-C DOCK2KO clone 19 and Cornelius DOCK2KO clone 19)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Severe combined immunodeficiency

  4759. PMUi002-A-2 (UCB144-CT2-C DOCK2KO clone 20 and Cornelius DOCK2KO clone 20)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Severe combined immunodeficiency

  4760. PMUi002-A-3 (Cornelius DOCK2KO clone 22 and UCB144-CT2-C DOCK2KO clone 22)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Severe combined immunodeficiency

  4761. PMUi002-B (Gustav and UCB144-CT1-G)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal (average)

  4762. PNUi004-A

    Japan Department of Psychiatry, Nagoya University Graduate School of Medicine (PNU)
    Disease:

    Schizophrenia

  4763. PNUi004-B

    Japan Department of Psychiatry, Nagoya University Graduate School of Medicine (PNU)
    Disease:

    Schizophrenia

  4764. PNUi004-C

    Japan Department of Psychiatry, Nagoya University Graduate School of Medicine (PNU)
    Disease:

    Schizophrenia

  4765. PNURCKi001-A (CK-iAT1)

    South Korea Pusan National University Yangsan Hospital, Rare Disease Center (PNURCK)
    Disease:

    Arts syndrome

  4766. PNURCKi002-A (CK-iCD1)

    South Korea Pusan National University Yangsan Hospital, Rare Disease Center (PNURCK)
    Disease:

    Citrin deficiency

  4767. PNURCKi003-A (CK-iDS1)

    South Korea Pusan National University Yangsan Hospital, Rare Disease Center (PNURCK)
    Disease:

    Desanto-shinawi syndrome

  4768. PNUSCRi001-A (GBA PD iPSC7)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Parkinson disease

  4769. PNUSCRi002-A (GBA PD iPSC9)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Parkinson disease

  4770. PNUSCRi003-A (GBA Gaucher iPSC1)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Gaucher disease

  4771. PNUSCRi004-A (GBA PD iPSC8)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Parkinson disease

  4772. PNUSCRi005-A

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Hunter syndrome

  4773. PNUSCRi006-A (Sanfilippo hiPSCs)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Sanfilippo syndrome

  4774. PNUYHi002-A

    South Korea Pusan National University Yangsan Hospital (PNUYH)
    Disease:

    Alzheimer's disease

  4775. PNUYHi003-A

    South Korea Pusan National University Yangsan Hospital (PNUYH)
    Disease:

    Neuronal intranuclear inclusion disease

  4776. PSXi015-A (RUCDRi002-A and TC-1133)

    United States Pluristyx (PSX)
    Disease:

    Normal (average)

  4777. PUFHi004-A (TMEM163 c.227T>C p.(Leu76Pro) iPSC)

    China Peking University First Hospital (PUFH)
    Disease:

    Leukodystrophy

  4778. PUMCi002-A (AF-iPSCs and C1)

    China Peking Union Medical College (PUMC)
    Disease:

    Normal (average)

  4779. PUMCi006-A

    China Peking Union Medical College (PUMC)
    Disease:

    Alzheimer disease

  4780. PUMCHi001-A (IPS-34)

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Familial partial lipodystrophy type 2

  4781. PUMCHi001-A-1 (IPS34-R-17)

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Familial partial lipodystrophy type 2

  4782. PUMCHi002-A (20180908R-AE3 and PUMCH-IRC)

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Restrictive cardiomyopathy

  4783. PUMCHi004-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Hereditary systemic amyloidosis 1

  4784. PUMCHi005-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Transthyretin cardiac amyloidosis

  4785. PUMCHi019-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Autosomal dominant optic atrophy plus syndrome

  4786. PUMCHi020-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Aicardi-goutieres syndrome

  4787. PVDMMi001-A (NG2266)

    Italy Molecular Medicine Department - University of Pavia (unipv) (PVDMM)
    Disease:

    Joubert syndrome

  4788. PVDMMi002-A (NG5925)

    Italy Molecular Medicine Department - University of Pavia (unipv) (PVDMM)
    Disease:

    Joubert syndrome

  4789. PVDMMi003-A (NG2685)

    Italy Molecular Medicine Department - University of Pavia (unipv) (PVDMM)
    Disease:

    Joubert syndrome

  4790. PVDMMi004-A (NG4713)

    Italy Molecular Medicine Department - University of Pavia (unipv) (PVDMM)
    Disease:

    Joubert syndrome

  4791. QBRIi001-A (Ctr1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  4792. QBRIi001-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  4793. QBRIi001-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  4794. QBRIi002-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  4795. QBRIi002-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  4796. QBRIi002-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  4797. QBRIi005-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  4798. QBRIi005-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  4799. QBRIi005-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  4800. QBRIi006-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  4801. QBRIi006-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  4802. QBRIi006-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  4803. QBRIi007-A (GLUT2 Mut-int iPSCs)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Fanconi-bickel syndrome

  4804. QBRIi009-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Central hypothyroidism

  4805. QBRIi013-A

    Qatar Qatar Biomedical Research Institute (QBRI)

  4806. QBRIi014-A (NDD01 and hiPSC_11080401_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4807. QBRIi015-A (NDD04 and hiPSC_11080404_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4808. QBRIi016-A (NDD05 and hiPSC_11080405_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4809. QBRIi017-A (CtrlM and hiPSC_11080402_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  4810. QBRIi018-A (hiPSC_11080403_c1 and CtrlF)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  4811. QBRIi019-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4812. QBRIi020-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4813. QBRIi021-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4814. QBRIi021-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4815. QBRIi022-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4816. QBRIi022-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4817. QBRIi023-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4818. QBRIi023-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4819. QBRIi024-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4820. QBRIi024-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4821. QBRIi025-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4822. QBRIi025-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  4823. QBRIi026-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  4824. QBRIi027-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  4825. QBRIi027-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal (average)

  4826. RAUi001-A

    Armenia Russian-Armenian University (RAU)
    Disease:

    Normal (average)

  4827. RAUi001-B

    Armenia Russian-Armenian University (RAU)
    Disease:

    Normal (average)

  4828. RAUi001-C

    Armenia Russian-Armenian University (RAU)
    Disease:

    Normal (average)

  4829. RAUi002-A

    Armenia Russian-Armenian University (RAU)
    Disease:

    Familial mediterranean fever

  4830. RBi001-A (fb101 and RB101)

    United Kingdom R Biomedical (RB)
    Disease:

    Normal (average)

  4831. RCi004-A (PDSC-10 and RCi150)

    United Kingdom Roslin Cells (RC)
    Disease:

    Huntington disease

  4832. RCi004-B (RCi68 and PDSC-3)

    United Kingdom Roslin Cells (RC)
    Disease:

    Huntington disease

  4833. RCi005-A (FB71c4 and RCi171)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  4834. RCi006-A (FB69c4 and RCi169)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  4835. RCi007-A (FB70c1 and RCi170)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  4836. RCi007-C

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  4837. RCi009-A (Rci201 and FB73c6)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  4838. RCMGi001-A (P1L5)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  4839. RCMGi002-A (P7L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  4840. RCMGi004-A (P6L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  4841. RCMGi004-B (P6L8)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  4842. RCMGi005-A (P5L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  4843. RCMGi005-B (P5L5)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  4844. RCMGi006-A (VII_MAK_C)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Normal (average)

  4845. RCMGi007-A (P8L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  4846. RCMGi008-A (P9L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  4847. RCMGi009-A (P14L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Fibrodysplasia ossificans progressiva

  4848. RCMGi011-A (P10L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Mucopolysaccharidosis type ivb

    Disease:

    Autosomal recessive nonsyndromic deafness 12

  4849. RCMGi011-B (P10L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Mucopolysaccharidosis type ivb

    Disease:

    Autosomal recessive nonsyndromic deafness 12

  4850. RCMGi012-A (P11L3)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Maroteaux-lamy syndrome

  4851. RCMGi013-A (P2L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  4852. RCMGi014-A (P20L7)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Fibrodysplasia ossificans progressiva

  4853. RCMGi015-A (P16L4)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Glycogen storage disease i

  4854. RCMGi016-A (P17L16)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Glycogen storage disease i

  4855. RCMGi017-A (P12L3)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Normal (average)

  4856. RCMGi018-A (P22L5)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Duchenne muscular dystrophy

  4857. RCNSi003-A (2GMB7)

    Hungary RCNS-Institute of Molecular Life Sciences (RCNS)
    Disease:

    Normal (average)

  4858. 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

  4859. 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

  4860. 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

  4861. 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

  4862. 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)

  4863. 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)

  4864. 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

  4865. 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)

  4866. 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

  4867. 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

  4868. 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

  4869. 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

  4870. 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

  4871. 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)

  4872. 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)

  4873. 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)

  4874. 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

  4875. RCSIi001-A (iPDK)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Normal (average)

  4876. RCSIi002-A (iDFU8)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Diabetes mellitus

  4877. RCSIi003-A (iNFF12)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Normal (average)

  4878. RCSIi004-A (iNFF14)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Normal (average)

  4879. RCSIi005-A (iDFF24)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Diabetes mellitus

  4880. REGUi001-A (IPS4FLV)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  4881. REGUi002-A (IPS6FLV)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  4882. 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

  4883. REGUi016-A (4F_Tie2_RNA190)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  4884. REGUi016-C (4F_Tie2_Sv190)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  4885. REGUi016-D (4F_PBMC_Sv190)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  4886. REGUi017-A (4F_Tie2_RNA191)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  4887. REGUi017-C (4F_Tie2_Sv191)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  4888. REGUi017-D (4F_PBMC_Sv191)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  4889. REGUi018-A (4F_Tie2_RNA192)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  4890. REGUi018-C (4F_Tie2_Sv192)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  4891. REGUi018-D (4F_PBMC_Sv192)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Normal (average)

  4892. RFSCi001-A (RFSC3)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  4893. RFSCi002-A (RFSC4)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Age-related macular degeneration

  4894. RFSCi003-A (RFSC22)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  4895. RFSCi004-A (RFSC23)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Age-related macular degeneration

  4896. RFSCi005-A (RFSC18)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  4897. RFSCi006-A (RFSC19)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Age-related macular degeneration

  4898. RFSCi007-A (RFSC10)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  4899. RFSCi008-A (RFSC16)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  4900. RIi001-A (R.1.H.iPSC.1)

    Iran Royan Institute (RI)

  4901. RIi002-A (BOM.1.H.iPSC.1)

    Iran Royan Institute (RI)
    Disease:

    Normal (average)

  4902. RIi003-A (FHC.1.H.iPSC.3)

    Iran Royan Institute (RI)
    Disease:

    Familial hypercholesterolemia

  4903. RIi004-A (GSD.1.H.iPSC.7)

    Iran Royan Institute (RI)
    Disease:

    Glycogen storage disease

  4904. RIi005-A (TYR.1.H.iPSC.1)

    Iran Royan Institute (RI)
    Disease:

    Tyrosinemia type 1

  4905. RIi006-A (HER.1.H.iPSC.1)

    Iran Royan Institute (RI)
    Disease:

    Cholestasis

  4906. RIi007-A (R.1.H.iPSC.4)

    Iran Royan Institute (RI)

  4907. RIi008-A (R.1.H.iPSC.9)

    Iran Royan Institute (RI)

  4908. RIi009-A (RP2.H.iPSC.3)

    Iran Royan Institute (RI)
    Disease:

    Retinitis pigmentosa

  4909. RIi010-A (LCA.1.H.iPSC.1)

    Iran Royan Institute (RI)
    Disease:

    Leber congenital amaurosis

  4910. RIi011-A (USH.1.H.iPSC.6)

    Iran Royan Institute (RI)
    Disease:

    Usher syndrome

  4911. RIi012-A (RP.1.H.iPSC.2)

    Iran Royan Institute (RI)
    Disease:

    Retinitis pigmentosa

  4912. RIi013-A (ARMD.1.H.iPSC.2)

    Iran Royan Institute (RI)
    Disease:

    Age-related macular degeneration

  4913. RIi014-A (LHON.1.H.iPSC.5)

    Iran Royan Institute (RI)
    Disease:

    Leber congenital amaurosis

  4914. RIi015-A (CNS.1.H.iPSC.10)

    Iran Royan Institute (RI)
    Disease:

    Crigler-najjar syndrome

  4915. RIi016-A (CNS.2.H.iPSC.7)

    Iran Royan Institute (RI)
    Disease:

    Crigler-najjar syndrome

  4916. UCSFi001-A-87

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Tuberous sclerosis 2

  4917. RMCGENi005-A

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  4918. RMCGENi005-A-1

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  4919. SCTCi017-A-1

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  4920. SCTCi018-A-1

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  4921. RMCGENi020-A (IPS15-00004)

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  4922. RMCGENi021-A (IPS22-00087)

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  4923. RNRMUi001-A (RDEB-iPSC-d1)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Epidermolysis bullosa dystrophica, autosomal recessive

  4924. RNRMUi002-A (RDEB-iPSC-d2)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Epidermolysis bullosa dystrophica, autosomal recessive

  4925. RNRMUi003-A (RDEB-iPSC-d3A)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Epidermolysis bullosa dystrophica, autosomal recessive

  4926. KUIFMSi004-A-1 (hPSC MPP8 Neon Green)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Normal (average)

  4927. 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

  4928. RNRMUi006-A (RDEB-IPSC-d10)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Recessive dystrophic epidermolysis bullosa

  4929. RNRMUi007-A (EBS-iPSC-d12)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Epidermolysis bullosa simplex 2f, with mottled pigmentation

  4930. RTIBDi001-A (MCND-TENS2)

    United States Regenerative Therapies for Inherited Blood Disorder (RTIBD)
    Disease:

    Normal (average)

  4931. 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)

  4932. SANi011-A (PE1S40 cl.D and FLI1 clone D)

    Netherlands Sanquin (SAN)
    Disease:

    Bleeding disorder, platelet-type, 21

  4933. SANi012-A (ETV6 cl.6 and PE1L103 cl.6)

    Netherlands Sanquin (SAN)
    Disease:

    Thrombocytopenia 5

  4934. SANi013-A (TRACER #P5 clone F)

    Netherlands Sanquin (SAN)
    Disease:

    Diamond-blackfan anemia

  4935. SAPi002-A (ALS I, ALS I–FUS-R514S/wt and FUS-R514S/wt)

    Italy Sapienza University of Rome (SAP)
    Disease:

    Amyotrophic lateral sclerosis

  4936. SAPi003-A (ALS II, FUS-R521C/wt and ALS II–FUS-R521C/wt)

    Italy Sapienza University of Rome (SAP)
    Disease:

    Amyotrophic lateral sclerosis

  4937. SAPi004-A (ALS III, TDP43-A382T/A382T and ALS III-TDP43-A382T/A382T)

    Italy Sapienza University of Rome (SAP)
    Disease:

    Amyotrophic lateral sclerosis

  4938. SBIi006-A (SC102A-1)

    United States System Biosciences (SBI)
    Disease:

    Normal (average)

  4939. SBWCHi001-A

    China Shenzhen Baoan Women's and Children's Hospital, Jinan University (SBWCH)
    Disease:

    Ctnnb1 gene mutation

  4940. SCAUi001-A

    China South China Agricultural University (SCAU)
    Disease:

    Normal (average)

  4941. SCAUi001-A-1

    China South China Agricultural University (SCAU)
    Disease:

    Cone-rod dystrophy

  4942. SCAUi001-A-2

    China South China Agricultural University (SCAU)
    Disease:

    Retinitis pigmentosa

  4943. SCHi001-A

    South Korea Severance Children’s Hospital (SCH)
    Disease:

    Adrenoleukodystrophy

  4944. SCHi001-A-1 (AMN5-Corrected iPSC)

    South Korea Severance Children’s Hospital (SCH)
    Disease:

    Adrenoleukodystrophy

  4945. SCIKFi001-A (D3-iR-2)

    Indonesia Stem Cell and Cancer Institute, PT. Kalbe Farma Tbk. (SCIKF)
    Disease:

    Normal (average)

  4946. SCIKFi001-B (D3-iE)

    Indonesia Stem Cell and Cancer Institute, PT. Kalbe Farma Tbk. (SCIKF)
    Disease:

    Normal (average)

  4947. SCMCi001-A

    China Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine (SCMC)
    Disease:

    Normal (average)

  4948. SCMCi001-A-1

    China Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine (SCMC)
    Disease:

    Congenital heart disease

  4949. SCTi001-A (STiPS-F016)

    Canada STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  4950. SCTi002-A (STiPS-M001)

    Canada STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  4951. SCTi003-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  4952. SCTi003-A-1

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Alzheimer's disease

  4953. SCTi003-A-2

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Alzheimer's disease

  4954. SCTi003-A-3

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Stargardt disease

  4955. SCTi004-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  4956. SCTi005-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  4957. SCTi006-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  4958. SCTCi008-A (IPS17-00095)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  4959. SCTCi009-A (IPS17-00097)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  4960. SCTCi010-A (IPS17-00041)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  4961. SCTCi011-A (IPS18-00072)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  4962. SCTCi012-A (IPS19-00027)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  4963. SCTCi013-A (IPS19-00053)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  4964. SCTCi014-A (IPS17-00056)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  4965. SCTCi014-A-1 (IPS17-00056 Crispr clone O5)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  4966. SCTCi015-A (IPS19-00051)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  4967. SCTCi015-A-1 (IPS19-00051 Crispr clone H6)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  4968. SCTCi016-A (IPS18-00092)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Leber congenital amaurosis

  4969. SCTCi017-A (IPS15-00006)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Stargardt disease

  4970. SCTCi018-A (IPS15-00007)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Stargardt disease

  4971. SCTCi020-A (IPS17-00028)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  4972. SCTCi021-A (IPS17-00027)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  4973. SCTCi022-A (IPS17-00042)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  4974. SCTCi023-A (IPS17-00063)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Self-limited familial neonatal epilepsy

  4975. SCTCi024-A (IPS18-00047)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  4976. SCTCi025-A (IPS18-00095)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Self-limited familial neonatal epilepsy

  4977. SCTCi026-A (IPS22-00005)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Pyridoxine-dependent epilepsy

  4978. SCTCi027-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Pyridoxine-dependent epilepsy

  4979. SCTCi028-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Pyridoxine-dependent epilepsy

  4980. SCTCi029-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Pyridoxine-dependent epilepsy

  4981. SCTCi030-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Glutaric acidemia type 1

  4982. SCTCi031-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Glutaric acidemia type 1

  4983. SCTCi032-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Glutaric acidemia type 1

  4984. SCTCi033-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Glutaric acidemia type 1

  4985. SCTCi037-A (IPS19-00015)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  4986. SCTCi037-A-1 (EPC26.1.1)

    Belgium Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  4987. SCTCi039-A (IPS19-00092)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  4988. SCTCi039-A-1 (NGC22.3.369)

    Belgium Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  4989. SCTCi041-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  4990. SCTCi042-A (IPS17-00036)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  4991. SCTCi046-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Corneal dystrophy, fuchs endothelial, 3

  4992. SCTCi047-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Corneal dystrophy, fuchs endothelial, 3

  4993. SCVIi030-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  4994. SCVIi031-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  4995. SCVIi036-A (SCVI248)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  4996. SCVIi037-A (SCVI672)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  4997. SCVIi049-A (SCVI104)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  4998. SCVIi050-A (SCVI2486)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  4999. SCVIi051-A (477)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5000. SCVIi053-A (2021)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5001. SCVIi055-A (SCVI868 and SCVI-868)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5002. SCVIi056-A (SCVI956 and SCVI-956)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5003. SCVIi057-A (SCVI-975 and SCVI975)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5004. SCVIi059-A (SCVIi2413)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5005. SCVIi060-A (SCVi2506)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5006. SCVIi061-A (SCVI2149C1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome

  5007. SCVIi062-A (SCVI2150c1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome

  5008. SCVIi066-A (SCVI2047)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Cardiac attr amyloidosis

  5009. SCVIi067-A (SCVI2742)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Cardiac attr amyloidosis

  5010. SCVIi073-A (SCVIi574C2)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5011. SCVIi074-A (SCVIi599C1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5012. SCVIi075-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Spinal muscular atrophy

  5013. SCVIi076-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Spinal muscular atrophy

  5014. SCVIi077-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  5015. SCVIi078-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  5016. SCVIi079-A (SCVI167 and PHBI-ST-036)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Idiopathic pulmonary hypertension

  5017. SCVIi080-A (PHBI-ST-040 and SCVI171)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Idiopathic pulmonary hypertension

  5018. SCVIi081-A (SCVI2535)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5019. SCVIi082-A (SCVI2838)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5020. SCVIi083-A (SCVI2655)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5021. SCVIi084-A (SCVI2591)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5022. SCVIi085-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Down syndrome

  5023. SCVIi086-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Down syndrome

  5024. SCVIi087-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Duchenne muscular dystrophy

  5025. SCVIi088-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Duchenne muscular dystrophy

  5026. SCVIi091-A (SCVI2617)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hereditary systemic amyloidosis 1

  5027. SCVIi092-A (SCVI2628)

    United States Stanford Cardiovascular Institute (SCVI)

  5028. SCVIi096-A (SCVI-675fs1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5029. SCVIi097-A (SCVI-675fs2)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5030. SCVIi098-A (SCVI-675fs3)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5031. SCVIi099-A (SCVI-675fs4)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5032. SCVIi100-A (SCVI2009A)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5033. SCVIi101-A (SCVI926A)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  5034. SCVIi104-A (SCVIi2996)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Li-fraumeni syndrome

  5035. SCVIi105-A (SCVIi3001)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Li-fraumeni syndrome

  5036. SCVIi106-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Williams syndrome

  5037. SCVIi107-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Williams syndrome

  5038. SCVIi108-A (SCVI2767)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Familial hypercholesterolemia

  5039. SCVIi109-A (SCVI3020)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Familial hypercholesterolemia

  5040. SCVIi110-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome 1

  5041. SCVIi111-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome 1

  5042. SCVIi114-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Lynch syndrome

  5043. SCVIi115-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Lynch syndrome

  5044. SCVIi116-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Phace syndrome

  5045. SCVIi117-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Phace syndrome

  5046. SCVIi118-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Phace syndrome

  5047. SCVIi121-A (SCVI 488)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5048. SCVIi123-A (SCVI 2176)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5049. SCVIi124-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Loeys-dietz syndrome 1

  5050. SCVIi125-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Loeys-dietz syndrome 1

  5051. SCVIi126-A (SCVI2899)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Facioscapulohumeral muscular dystrophy

  5052. SCVIi127-A (SCVI2830)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Facioscapulohumeral dystrophy

  5053. SCVIi128-A (SCVI766)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Marfan syndrome

  5054. SCVIi129-A (SCVI2454)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Marfan syndrome

  5055. SCVIi132-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5056. SCVIi134-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Myotonic dystrophy type 1

  5057. SCVIi135-A (SCVI3161)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5058. SCVIi136-A (SCVI3171)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  5059. SCVIi137-A (SCVI 770)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Myotonic dystrophy type 1

  5060. SCVIi138-A (SCVI2741)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Thoracic aortic aneurysm

  5061. SCVIi139-A (SCVI2925)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Thoracic aortic aneurysm

  5062. SCVIi140-A (iPSC3503)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5063. SCVIi141-A (iPSC3880)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5064. SCVIi142-A (SCVI2900 and SCVI2900C1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Pten hamartoma tumor syndrome

  5065. SCVIi143-A (SCVI3215 and SCVI3215C1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Pten hamartoma tumor syndrome

  5066. SCVIi145-A (SCVI997)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Emery-dreifuss muscular dystrophy

  5067. SCVIi146-A (SCVI3443)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  5068. SCVIi154-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5069. SCVIi155-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5070. SCVIi158-A (SCVI2930)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5071. SCVIi159-A (SCVI3070)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  5072. SCVIi162-A (SCVI3067)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5073. SCVIi163-A (SCVI3354)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  5074. SDASi001-A

    China Qilu University of Technology(Shandong Academy of Sciences) (SDAS)
    Disease:

    Schimke immuno-osseous dysplasia

  5075. SDCHi001-A

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Normal (average)

  5076. SDCHi005-A (DEPDC5-ZHW)

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Epilepsy

  5077. SDCHi007-A (RY-5)

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Epilepsy

  5078. SDCHi008-A (CX2)

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Epilepsy

  5079. SDCHi009-A (RY6)

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Epilepsy

  5080. SDCHi011-A

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Normal (average)

  5081. SDHi001-A (MVPSDHi001)

    China The Fourth Affiliated Hospital of Soochow University(Suzhou Dushu Lake Hospital) (SDH)
    Disease:

    Mitral valve prolapse

  5082. SDPHi002-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Lung cancer

  5083. SDPHi003-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Normal (average)

  5084. SDPHi004-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Normal (average)

  5085. SDPHi005-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Normal (average)

  5086. SDPHi006-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Normal (average)

  5087. SDPHi007-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Alagille syndrome

  5088. SDQLCHi028-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Xia-gibbs syndrome

  5089. SDQLCHi030-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Lesch-nyhan syndrome

  5090. SDQLCHi043-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)

  5091. SDQLCHi050-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Normal (average)

  5092. SDQLCHi054-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Mental retardation, autosomal dominant 5

  5093. SDQLCHi059-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Congenital disorder of deglycosylation

  5094. SDQLCHi061-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Carbamoyl phosphate synthetase i deficiency disease

  5095. SDQLCHi062-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Focal segmental glomerulosclerosis 7

  5096. SDQLCHi063-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Maturity-onset diabetes of the young type 2

  5097. SDQLCHi064-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Canavan disease

  5098. SDQLCHi065-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Down syndrome

  5099. SDQLCHi066-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Th-deficient dopa-responsive dystonia

  5100. SDQLCHi067-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Subcortical band heterotopia

  5101. SDQLCHi068-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Immunodeficiency 14a, autosomal dominant

  5102. SDQLCHi072-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Autism spectrum disorder due to auts2 deficiency

  5103. SDQLCHi073-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Cockayne syndrome

  5104. SDQLCHi079-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Johanson-blizzard syndrome

  5105. SDQLCHi080-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Gm1 gangliosidosis

  5106. SDQLCHi081-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Rahman syndrome

  5107. SDQLCHi083-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Autosomal recessive cutis laxa type iid

  5108. SDQLCHi084-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Clark-baraitser syndrome

  5109. SDUBMSi001-A

    China School of Basic Medical Sciences, Shandong University (SDUBMS)
    Disease:

    Hereditary spastic paraplegia

  5110. SDUCHi001-A

    China Children’s Hospital Affiliated to Shandong University (SDUCH)
    Disease:

    Normal (average)

  5111. SDZFYi001-A

    China Shandong Academy of Occupational Health and Occupational Medicine (SDZFY)
    Disease:

    Normal (average)

  5112. SEUi001-A

    China Southeast University (SEU)
    Disease:

    Normal (average)

  5113. SFMUi001-A

    China Shandong First Medical University (SFMU)
    Disease:

    Usher syndrome type 2

  5114. SFPHi001-A

    China Shanghai Fifth People’s Hospital (SFPH)
    Disease:

    Hereditary antithrombin deficiency

  5115. SHCDNi001-A (SHCDN001)

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Mitochondrial dna depletion syndrome

  5116. SHCDNi002-A (SHCDN002)

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Fg syndrome

    Disease:

    Lujan-fryns syndrome

  5117. SHCDNi003-A

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Allan-herndon-dudley syndrome

  5118. SHCDNi006-A (SHCDN006)

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Epilepsy

  5119. SHCDNi007-A

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Pyruvate carboxylase deficiency

  5120. SHCDNRi001-A (IPS-51)

    China Shanghai Children's Hospital, Department of Nephrology and Rheumatology (SHCDNR)
    Disease:

    Alport syndrome

  5121. SHEHi002-A (iPS36)

    China Shanghai East Hospital (SHEH)
    Disease:

    Long qt syndrome 8

  5122. SHEHDNi001-A

    China Department of Neurology (SHEHDN)
    Disease:

    Obsolete_alzheimer's disease

  5123. SHEHDNi002-A (KY03AP)

    China Department of Neurology (SHEHDN)
    Disease:

    Parkinson disease

  5124. SHETi001-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Floating-harbor syndrome

  5125. SHETi002-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Arrhythmia

  5126. SHETi003-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  5127. SHETi004-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Left bundle branch block artifact

  5128. SHETi005-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Normal (average)

  5129. SHFDi001-A (SHFD-1)

    China Shanghai Stomatological Hospital, Fudan University, Shanghai, China (SHFD)
    Disease:

    Ankylosing spondylitis

  5130. SHIPMi001-A

    China Shanghai Institute of Precision Medicine (SHIPM)
    Disease:

    Hypertrophic cardiomyopathy

  5131. SHIPMi002-A

    China Shanghai Institute of Precision Medicine (SHIPM)
    Disease:

    Normal (average)

  5132. SHTCMi001-A

    China Affiliated Hospital of Shandong University of Traditional Chinese Medicine (SHTCM)
    Disease:

    X-linked alport syndrome

  5133. SHUPLi001-A (IPS-14)

    China Shanghai University of Political Science and Law (SHUPL)
    Disease:

    Normal (average)

  5134. SHUPLi002-A (iPS-26)

    China Shanghai University of Political Science and Law (SHUPL)
    Disease:

    Normal (average)

  5135. SIAISi001-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Obsolete_alzheimer's disease

  5136. SIAISi002-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5137. SIAISi003-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Obsolete_alzheimer's disease

  5138. SIAISi004-A (ZYF)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Obsolete_alzheimer's disease

  5139. SIAISi006-A (JJY)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Alzheimer's disease

  5140. SIAISi007-A (ZSJ)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Alzheimer's disease

  5141. SIAISi008-A (ZMY)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Obsolete_alzheimer's disease

  5142. SIAISi009-A (YJP)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Mild cognitive impairment

  5143. SIAISi010-A (16F0040)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5144. SIAISi011-A (NZM)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5145. SIAISi012-A (QHL)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5146. SIAISi016-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Alzheimer's disease

  5147. SIAISi017-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5148. SIAISi018-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5149. SIAISi019-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal (average)

  5150. SIAISi020-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Mild cognitive impairment

  5151. SIAISi021-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Obsolete_alzheimer's disease

  5152. SIAISi022-A

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Alzheimer's disease

  5153. SIGi001-A (IPSC0028 parental and SAMEA4447455)

    United States Sigma-Aldrich (SIG)
    Disease:

    Normal (average)

  5154. SIGi001-A-1 (iPSC0028 SLC17A7/GFP E3)

    United States Sigma-Aldrich (SIG)
    Disease:

    Normal (average)

  5155. SIGi001-A-2 (iPSC0028 SLC17A7/GFP C3)

    United States Sigma-Aldrich (SIG)
    Disease:

    Normal (average)

  5156. SIGi001-A-3 (iPSC0028 MAPT P301L C4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5157. SIGi001-A-4 (iPSC0028 MAPT P301L D4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5158. SIGi001-A-5 (iPSC0028 MAPT P301S 1C9C4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5159. SIGi001-A-6 (iPSC0028 MAPT P301S 1B9C9)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5160. SIGi001-A-7 (iPSC0028 MAPT P301S 2G2B7)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5161. SIGi001-A-8 (iPSC0028 MAPT P301S+Ex10+16/Clone 7D11A7)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  5162. SIGi001-A-9 (iPSC0028 MAPT P301S+Ex10+16/Clone 7H6A1)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  5163. SIGi001-A-10 (iPSC0028 MAPT P301S+Ex10+16/Clone 7G4A8)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  5164. 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

  5165. SIGi001-A-12 (iPSC0028 - BiAllelic MAPT_Ex10+16T/Clone 1F5-D12 and SAMEA104237570)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  5166. SIGi001-A-13 (iPSC0028 – MonoAllelic MAPT_Ex10+16T/Clone 1D01-11)

    United States Sigma-Aldrich (SIG)
    Disease:

    Alzheimer disease

  5167. SIPDi001-A (Li-Campeau syndrome)

    China Shaanxi Institute of Pediatric Diseases (SIPD)
    Disease:

    Li-campeau syndrome

  5168. SJTUi003-A

    China Shanghai Jiao Tong University School of Medicine (SJTU)
    Disease:

    Alzheimer's disease

  5169. SJTUGHi001-A

    China Shanghai General Hospital (SJTUGH)
    Disease:

    Retinitis pigmentosa

  5170. SJTUGHi002-A

    China Shanghai General Hospital (SJTUGH)
    Disease:

    Retinitis pigmentosa

  5171. SJTUGHi004-A

    China Shanghai General Hospital (SJTUGH)
    Disease:

    Best vitelliform macular dystrophy

  5172. SJTUXHi001-A

    China Shanghai Xinhua Hospital (SJTUXH)
    Disease:

    Autism

  5173. SJTUXHi002-A

    China Shanghai Xinhua Hospital (SJTUXH)
    Disease:

    Autism

  5174. SJTUXHi003-A

    China Shanghai Xinhua Hospital (SJTUXH)
    Disease:

    Familial exudative vitreoretinopathy

  5175. SJTUXHi004-A

    China Shanghai Xinhua Hospital (SJTUXH)
    Disease:

    Retinoblastoma

  5176. SKi001-A (PGPC3-75 and SK1)

    Canada Hospital for Sick Children (SK)
    Disease:

    Normal (average)

  5177. SKi003-A (PGPC17-11 and SK2)

    Canada Hospital for Sick Children (SK)
    Disease:

    Normal (average)

  5178. SKi004-A (PGPC14-26 and SK4)

    Canada Hospital for Sick Children (SK)
    Disease:

    Normal (average)

  5179. SKLOi004-A

    China State Key Laboratory of Ophthalmology (SKLO)
    Disease:

    Retinoblastoma

  5180. SKLOi004-B

    China State Key Laboratory of Ophthalmology (SKLO)
    Disease:

    Retinoblastoma

  5181. SKLOi005-A

    China State Key Laboratory of Ophthalmology (SKLO)
    Disease:

    Leber congenital amaurosis

  5182. SKLOi005-B

    China State Key Laboratory of Ophthalmology (SKLO)
    Disease:

    Leber congenital amaurosis

  5183. SKLRMi001-A

    China State Key Laboratory of Reproductive Medicine, Nanjing Medical University (SKLRM)
    Disease:

    Androgen insensitivity syndrome

  5184. SKLRMi001-A-1 (AR repaired iPSCs)

    China State Key Laboratory of Reproductive Medicine, Nanjing Medical University (SKLRM)
    Disease:

    Androgen insensitivity syndrome

  5185. SMBCi002-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Clubfoot

  5186. SMBCi009-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Familial hypercholesterolemia

  5187. SMBCi010-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Multiple osteochondromas

  5188. SMBCi011-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Prader-willi syndrome

  5189. SMBCi013-A (WD-iPSC)

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Hepatolenticular degeneration

  5190. SMBCi014-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Osteogenesis imperfecta

  5191. SMBCi018-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Clubfoot

  5192. SMBCi022-A (5003)

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Fabry disease

  5193. SMCPGHi001-A (SMCPGHi-ABCA3)

    China The Seven Medical Center of PLA General Hospital (SMCPGH)
    Disease:

    Pulmonary surfactant metabolism dysfunction-3

  5194. SMUSHi002-A

    China Southern Medical University Shenzhen hospital (SMUSH)
    Disease:

    Normal (average)

  5195. SMUSHi003-A

    China Southern Medical University Shenzhen hospital (SMUSH)
    Disease:

    Focal segmental glomerulosclerosis

  5196. SMUSHi005-A

    China Southern Medical University Shenzhen hospital (SMUSH)
    Disease:

    X-linked dominant hypophosphatemic rickets

  5197. SMUSHi006-A

    China Southern Medical University Shenzhen hospital (SMUSH)
    Disease:

    Amyotrophic lateral sclerosis

  5198. SPHi001-A (SLEi002HZY)

    China Shenzhen People's Hospital (SPH)
    Disease:

    Systemic lupus erythematosus

  5199. SPPHIi003-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)

  5200. SPPHIi004-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)
    Disease:

    Alzheimer disease

  5201. SPPHIi005-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)
    Disease:

    Normal (average)

  5202. SPPHIi006-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)

  5203. SPPHIi007-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)
    Disease:

    Normal (average)

  5204. SSMCi001-A

    China The Fourth People's Hospital of Shenzhen (Shenzhen Samii Medical Center) (SSMC)
    Disease:

    Dilated cardiomyopathy

  5205. SSMCi002-A

    China The Fourth People's Hospital of Shenzhen (Shenzhen Samii Medical Center) (SSMC)
    Disease:

    Dilated cardiomyopathy

  5206. STBCi004-A (SFC832-03-19)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5207. STBCi004-B (SFC832-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5208. STBCi004-B-1 (SFC832-03-06 LRRK2WT/WT C47)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5209. STBCi004-C (SFC832-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5210. STBCi005-A (SFC833-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5211. STBCi005-B (SFC833-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5212. STBCi005-C (SFC833-03-14)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5213. STBCi006-A (SFC140-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5214. STBCi007-A (SFC855-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5215. STBCi007-B (SFC855-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5216. STBCi007-C (SFC855-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5217. STBCi009-A (SFC801-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5218. STBCi009-B (SFC801-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5219. STBCi009-C (SFC801-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5220. STBCi010-A (SFC802-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5221. STBCi011-A (SFC803-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5222. STBCi011-B (SFC803-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5223. STBCi011-C (SFC803-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5224. STBCi012-A (SFC805-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5225. STBCi012-B (SFC805-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5226. STBCi012-C (SFC805-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5227. STBCi013-A (SFC807-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5228. STBCi013-B (SFC807-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5229. STBCi014-A (SFC808-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5230. STBCi014-B (SFC808-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5231. STBCi014-C (SFC808-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5232. STBCi015-A (SFC809-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5233. STBCi015-B (SFC809-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5234. STBCi015-C (SFC809-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5235. STBCi016-A (SFC810-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5236. STBCi016-B (SFC810-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5237. STBCi016-C (SFC810-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5238. STBCi017-A (SFC811-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5239. STBCi017-B (SFC811-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5240. STBCi017-C (SFC811-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5241. STBCi018-A (SFC815-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5242. STBCi018-B (SFC815-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5243. STBCi018-C (SFC815-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5244. STBCi019-A (SFC828-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5245. STBCi019-B (SFC828-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5246. STBCi019-C (SFC828-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5247. STBCi020-A (SFC800-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5248. STBCi020-B (SFC800-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5249. STBCi023-A (SFC829-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5250. STBCi023-B (SFC829-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5251. STBCi023-C (SFC829-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5252. STBCi024-A (SFC831-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5253. STBCi024-B (SFC831-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5254. STBCi024-C (SFC831-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5255. STBCi025-A (SFC834-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5256. STBCi025-B (SFC834-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5257. STBCi025-C (SFC834-03-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5258. STBCi026-A (SFC840-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5259. STBCi026-A-1 (SFC840-03-03 LRRK2-/-D10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5260. STBCi026-A-2 (SFC840-03-03 LRRK2-/-C11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5261. STBCi026-A-3 (SFC840-03-03 LRRK2 WT/R1441C H3)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5262. STBCi026-A-4 (SFC840-03-03-PITX3-GFP)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5263. STBCi026-B (SFC840-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5264. STBCi026-C (SFC840-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5265. STBCi026-D (SFC840-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5266. STBCi027-A (SFC017-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5267. STBCi027-B (SFC017-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5268. STBCi028-A (SFC018-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5269. STBCi028-B (SFC018-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5270. STBCi028-C (SFC018-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5271. STBCi029-A (SFC020-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5272. STBCi029-B (SFC020-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5273. STBCi030-A (SFC023-03-24)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5274. STBCi030-B (SFC023-03-43)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5275. STBCi031-A (SFC024-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5276. STBCi031-B (SFC024-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5277. STBCi031-C (SFC024-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5278. STBCi032-A (SFC042-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5279. STBCi032-B (SFC042-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5280. STBCi033-A (SFC084-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5281. STBCi033-B (SFC084-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5282. STBCi033-C (SFC084-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5283. STBCi034-A (SFC091-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5284. STBCi034-B (SFC091-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5285. STBCi035-A (SFC813-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5286. STBCi035-B (SFC813-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5287. STBCi035-C (SFC813-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5288. STBCi036-A (SFC814-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5289. STBCi037-A (SFC816-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5290. STBCi037-B (SFC816-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5291. STBCi037-C (SFC816-03-13)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5292. STBCi038-A (SFC011-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5293. STBCi038-B (SFC011-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5294. STBCi038-C (SFC011-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5295. STBCi039-A (SFC062-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5296. STBCi039-B (SFC062-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5297. STBCi039-C (SFC062-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5298. STBCi040-A (SFC029-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5299. STBCi040-B (SFC029-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5300. STBCi040-C (SFC029-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5301. STBCi041-A (SFC081-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5302. STBCi041-B (SFC081-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5303. STBCi041-C (SFC081-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5304. STBCi042-A (SFC848-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5305. STBCi042-B (SFC848-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5306. STBCi042-C (SFC848-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5307. STBCi043-A (SFC120-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5308. STBCi043-B (SFC120-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5309. STBCi043-C (SFC120-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5310. STBCi044-A (SFC841-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5311. STBCi044-B (SFC841-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5312. STBCi045-A (SFC039-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5313. STBCi045-B (SFC039-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5314. STBCi045-C (SFC039-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5315. STBCi046-A (SFC021-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5316. STBCi046-B (SFC021-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5317. STBCi047-A (SFC043-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5318. STBCi047-B (SFC043-03-13)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5319. STBCi048-A (SFC014-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5320. STBCi048-B (SFC014-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5321. STBCi048-C (SFC014-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5322. STBCi049-A (SFC040-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5323. STBCi049-B (SFC040-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5324. STBCi049-C (SFC040-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5325. STBCi050-A (SFC041-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5326. STBCi050-B (SFC041-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5327. STBCi050-C (SFC041-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5328. STBCi051-A (SFC056-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5329. STBCi051-B (SFC056-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5330. STBCi051-C (SFC056-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5331. STBCi052-A (SFC086-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5332. STBCi052-B (SFC086-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5333. STBCi052-C (SFC086-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5334. STBCi053-A (SFC089-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5335. STBCi053-B (SFC089-03-55)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5336. STBCi053-C (SFC089-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5337. STBCi054-A (SFC010-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5338. STBCi054-B (SFC010-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5339. STBCi055-A (SFC026-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5340. STBCi055-B (SFC026-04-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5341. STBCi055-C (SFC026-04-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5342. STBCi056-A (SFC064-03-39)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5343. STBCi056-B (SFC064-03-42)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5344. STBCi056-C (SFC064-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5345. STBCi057-A (SFC065-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5346. STBCi057-B (SFC065-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5347. STBCi057-C (SFC065-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5348. STBCi058-A (SFC012-04-20)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5349. STBCi058-B (SFC012-04-30)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5350. STBCi058-C (SFC012-04-31)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5351. STBCi059-A (SFC015-01-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5352. STBCi059-B (SFC015-01-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5353. STBCi059-C (SFC015-01-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5354. STBCi060-A (SFC038-07-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5355. STBCi060-B (SFC038-07-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5356. STBCi060-C (SFC038-07-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5357. STBCi061-A (SFC850-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5358. STBCi062-A (SFC851-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5359. STBCi063-A (SFC856-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5360. STBCi063-B (SFC856-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5361. STBCi063-C (SFC856-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5362. STBCi064-A (SFC180-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5363. STBCi065-A (SFC853-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5364. STBCi066-A (SFC854-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5365. STBCi067-A (SFC855-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5366. STBCi068-A (SFC035-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5367. STBCi068-B (SFC035-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5368. STBCi068-C (SFC035-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5369. STBCi069-A (SFC050-03-21)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5370. STBCi069-B (SFC050-03-22)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5371. STBCi069-C (SFC050-03-20)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5372. STBCi070-A (SFC052-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5373. STBCi070-B (SFC052-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5374. STBCi071-A (SFC057-07-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5375. STBCi071-B (SFC057-07-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5376. STBCi071-C (SFC057-07-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5377. STBCi072-A (SFC058-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5378. STBCi072-B (SFC058-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5379. STBCi072-C (SFC058-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5380. STBCi073-A (SFC106-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5381. STBCi073-B (SFC106-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5382. STBCi074-A (SFC109-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5383. STBCi074-B (SFC109-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5384. STBCi074-C (SFC109-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5385. STBCi075-A (SFC129-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5386. STBCi075-B (SFC129-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5387. STBCi075-C (SFC129-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5388. STBCi076-A (SFC134-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5389. STBCi077-A (SFC136-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5390. STBCi077-B (SFC136-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5391. STBCi077-C (SFC136-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5392. STBCi078-A (SFC013-07-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5393. STBCi078-B (SFC013-07-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5394. STBCi078-C (SFC013-07-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5395. STBCi079-A (SFC045-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5396. STBCi079-B (SFC045-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5397. STBCi079-C (SFC045-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5398. STBCi080-A (SFC047-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5399. STBCi080-B (SFC047-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5400. STBCi080-C (SFC047-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5401. STBCi081-A (SFC170-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5402. STBCi081-B (SFC170-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5403. STBCi081-C (SFC170-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5404. STBCi082-A (SFC888-07-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5405. STBCi082-B (SFC888-07-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5406. STBCi082-C (SFC888-07-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5407. STBCi083-A (SFC830-04-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5408. STBCi083-B (SFC830-04-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5409. STBCi084-A (SFC871-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5410. STBCi084-B (SFC871-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5411. STBCi084-C (SFC871-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5412. STBCi085-A (SFC866-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5413. STBCi085-B (SFC866-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5414. STBCi085-C (SFC866-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5415. STBCi086-A (SFC842-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5416. STBCi086-B (SFC842-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5417. STBCi087-A (SFC845-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5418. STBCi087-B (SFC845-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5419. STBCi087-C (SFC845-03-11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5420. STBCi088-A (SFC872-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5421. STBCi088-B (SFC872-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5422. STBCi088-C (SFC872-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5423. STBCi089-A (SFC868-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5424. STBCi089-B (SFC868-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5425. STBCi089-C (SFC868-03-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5426. STBCi090-A (SFC867-04-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5427. STBCi090-B (SFC867-04-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5428. STBCi091-A (SFC126-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5429. STBCi091-B (SFC126-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5430. STBCi091-C (SFC126-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5431. STBCi092-A (SFC049-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5432. STBCi092-B (SFC049-03-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5433. STBCi092-C (SFC049-03-13)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5434. STBCi093-A (SFC893-07-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5435. STBCi093-B (SFC893-07-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5436. STBCi094-A (BPC321-01-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Drug-induced liver injury

  5437. STBCi094-B (BPC321-01-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Drug-induced liver injury

  5438. STBCi094-C (BPC321-01-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Drug-induced liver injury

  5439. STBCi095-A (BPC339-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Drug-induced liver injury

  5440. STBCi096-A (BPC340-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Congenital long qt syndrome

  5441. STBCi097-A (SFC055-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5442. STBCi097-B (SFC055-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5443. STBCi097-C (SFC055-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5444. STBCi098-A (SFC048-07-14)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5445. STBCi098-B (SFC048-07-18)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5446. STBCi098-C (SFC048-07-17)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5447. STBCi099-A (SFC059-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5448. STBCi099-B (SFC059-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5449. STBCi100-A (SFC117-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5450. STBCi101-A (SFC156-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5451. STBCi102-A (SFC163-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5452. STBCi103-A (SFC294-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5453. STBCi104-A (SFC836-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5454. STBCi105-A (SFC067-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5455. STBCi106-A (SFC068-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5456. STBCi107-A (SFC104-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5457. STBCi108-A (SFC110-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5458. STBCi109-A (SFC113-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5459. STBCi110-A (SFC116-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Age-related macular degeneration

  5460. STBCi111-A (SFC131-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5461. STBCi112-A (SFC177-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5462. STBCi113-A (SFC178-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5463. STBCi114-A (SFC034-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5464. STBCi115-A (SFC162-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5465. STBCi116-A (SFC164-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5466. STBCi117-A (SFC246-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5467. STBCi118-A (SFC037-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5468. STBCi119-A (SFC044-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5469. STBCi120-A (SFC046-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5470. STBCi121-A (SFC112-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5471. STBCi122-A (SFC115-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5472. STBCi123-A (SFC053-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5473. STBCi124-A (SFC135-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5474. STBCi125-A (SFC175-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5475. STBCi126-A (SFC105-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5476. STBCi127-A (SFC107-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  5477. STBCi128-A (SFC108-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5478. STBCi129-A (SFC137-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5479. STBCi130-A (SFC172-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5480. STBCi131-A (SFC295-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5481. STBCi132-A (SFC301-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5482. STBCi133-A (SFC302-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5483. STBCi134-A (SFC019-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5484. STBCi135-A (SFC033-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5485. STBCi136-A (SFC036-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5486. STBCi137-A (SFC076-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5487. STBCi138-A (SFC079-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5488. STBCi139-A (SFC101-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5489. STBCi140-A (SFC102-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5490. STBCi141-A (SFC103-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5491. STBCi142-A (SFC118-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5492. STBCi143-A (SFC122-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5493. STBCi144-A (SFC123-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5494. STBCi145-A (SFC125-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5495. STBCi146-A (SFC127-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5496. STBCi147-A (SFC128-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5497. STBCi148-A (SFC130-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5498. STBCi149-A (SFC132-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5499. STBCi150-A (SFC133-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5500. STBCi151-A (SFC145-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5501. STBCi152-A (SFC146-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5502. STBCi153-A (SFC147-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5503. STBCi154-A (SFC148-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5504. STBCi155-A (SFC149-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5505. STBCi156-A (SFC150-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5506. STBCi157-A (SFC154-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5507. STBCi158-A (SFC155-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5508. STBCi159-A (SFC158-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5509. STBCi160-A (SFC159-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5510. STBCi161-A (SFC160-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5511. STBCi162-A (SFC161-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5512. STBCi163-A (SFC165-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5513. STBCi164-A (SFC166-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5514. STBCi165-A (SFC168-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5515. STBCi166-A (SFC169-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5516. STBCi167-A (SFC174-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5517. STBCi168-A (SFC176-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5518. STBCi169-A (SFC179-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5519. STBCi170-A (SFC190-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5520. STBCi171-A (SFC191-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5521. STBCi172-A (SFC192-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5522. STBCi173-A (SFC193-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5523. STBCi174-A (SFC194-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5524. STBCi175-A (SFC195-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5525. STBCi176-A (SFC196-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5526. STBCi177-A (SFC197-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5527. STBCi178-A (SFC198-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5528. STBCi179-A (SFC243-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5529. STBCi180-A (SFC242-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5530. STBCi181-A (SFC247-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5531. STBCi182-A (SFC248-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5532. STBCi183-A (SFC250-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5533. STBCi184-A (SFC251-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5534. STBCi185-A (SFC253-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5535. STBCi186-A (SFC255-03-01 and SFC255-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5536. STBCi187-A (SFC256-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5537. STBCi188-A (SFC257-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5538. STBCi189-A (SFC258-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5539. STBCi190-A (SFC259-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5540. STBCi191-A (SFC260-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5541. STBCi192-A (SFC261-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5542. STBCi193-A (SFC262-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5543. STBCi194-A (SFC263-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5544. STBCi195-A (SFC286-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5545. STBCi196-A (SFC287-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5546. STBCi197-A (SFC288-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5547. STBCi198-A (SFC289-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5548. STBCi199-A (SFC290-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5549. STBCi200-A (SFC291-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5550. STBCi201-A (SFC292-03-02 and SFC292-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5551. STBCi202-A (SFC293-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5552. STBCi203-A (SFC296-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5553. STBCi204-A (SFC297-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5554. STBCi205-A (SFC298-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5555. STBCi206-A (SFC299-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5556. STBCi207-A (SFC300-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5557. STBCi208-A (SFC303-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5558. STBCi209-A (SFC304-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5559. STBCi210-A (SFC305-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5560. STBCi211-A (SFC306-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5561. STBCi212-A (SFC312-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5562. STBCi213-A (SFC313-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5563. STBCi214-A (SFC314-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5564. STBCi215-A (SFC318-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5565. STBCi216-A (SFC319-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5566. STBCi217-A (SFC320-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5567. STBCi218-A (SFC357-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5568. STBCi219-A (SFC358-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5569. STBCi220-A (SFC359-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5570. STBCi221-A (SFC360-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5571. STBCi222-A (SFC361-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5572. STBCi223-A (SFC363-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5573. STBCi224-A (SFC364-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5574. STBCi225-A (SFC365-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5575. STBCi226-A (SFC366-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5576. STBCi227-A (SFC367-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5577. STBCi228-A (SFC368-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5578. STBCi229-A (SFC369-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5579. STBCi230-A (SFC372-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5580. STBCi231-A (SFC374-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5581. STBCi232-A (SFC375-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  5582. STBCi233-A (SFC873-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5583. STBCi234-A (SFC874-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5584. STBCi235-A (SFC879-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5585. STBCi236-A (SFC880-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5586. STBCi237-A (SFC881-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5587. STBCi238-A (SFC882-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5588. STBCi239-A (SFC883-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5589. STBCi240-A (SFC884-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5590. STBCi241-A (SFC885-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5591. STBCi242-A (SFC886-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5592. STBCi243-A (SFC991-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5593. STBCi244-A (SFC993-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5594. STBCi245-A (SFC994-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5595. STBCi246-A (SFC995-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5596. STBCi247-A (SFC996-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5597. STBCi248-A (SFC999-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5598. STBCi249-A (SFC171-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  5599. STBCi250-A (SFC997-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5600. STBCi251-A (SFC998-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  5601. STBCi252-A (SFC254-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5602. STBCi253-A (SFC184-01-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5603. STBCi254-A (SFC143-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5604. STBCi255-A (SFC183-01-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5605. STBCi256-A (SFC144-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5606. STBCi257-A (SFC185-01-11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5607. STBCi258-A (SFC090-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5608. STBCi259-A (SFC032-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5609. STBCi260-A (SFC279-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5610. STBCi261-A (SFC186-01-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5611. STBCi262-A (SFC271-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5612. STBCi263-A (SFC268-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5613. STBCi264-A (SFC142-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5614. STBCi265-A (SFC121-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5615. STBCi266-A (SFC072-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5616. STBCi267-A (SFC027-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5617. STBCi268-A (SFC077-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5618. STBCi269-A (BPC943-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5619. STBCi270-A (BPC944-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5620. STBCi271-A (BPC936-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5621. STBCi272-A (BPC930-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5622. STBCi273-A (BPC928-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5623. STBCi274-A (BPC935-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5624. STBCi275-A (BPC937-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5625. STBCi276-A (BPC933-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5626. STBCi277-A (BPC934-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5627. STBCi278-A (SFC245-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5628. STBCi279-A (SFC063-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5629. STBCi280-A (SFC066-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5630. STBCi281-A (SFC167-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5631. STBCi282-A (SFC138-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5632. STBCi283-A (SFC073-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5633. STBCi284-A (BPC939-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5634. STBCi285-A (BPC940-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5635. STBCi286-A (BPC929-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5636. STBCi287-A (BPC946-04-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5637. STBCi288-A (SFC028-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5638. STBCi289-A (SFC030-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5639. STBCi290-A (SFC069-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5640. STBCi291-A (SFC080-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5641. STBCi292-A (SFC139-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5642. STBCi293-A (SFC843-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5643. STBCi294-A (SFC844-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5644. STBCi295-A (SFC847-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5645. STBCi295-B (SFC847-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5646. STBCi296-A (SFC864-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5647. STBCi297-A (SFC061-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5648. STBCi298-A (SFC865-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5649. STBCi299-A (BPC931-01-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5650. STBCi300-A (BPC932-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5651. STBCi301-A (BPC949-04-11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5652. STBCi302-A (BPC945-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5653. STBCi303-A (SFC071-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5654. STBCi304-A (SFC074-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5655. STBCi305-A (SFC083-03-10 and SFC083-07-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5656. STBCi306-A (SFC087-03-04 and SFC087-07-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5657. STBCi307-A (SFC088-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5658. STBCi308-A (SFC249-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5659. STBCi309-A (SFC391-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5660. STBCi310-A (SFC846-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5661. STBCi311-A (BPC941-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  5662. STBCi312-A (BPC333-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5663. STBCi313-A (BPC334-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5664. STBCi314-A (BPC335-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5665. STBCi315-A (BPC336-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  5666. STBCi316-A (SFC244-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5667. STBCi317-A (SFC241-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5668. STBCi318-A (SFC200-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5669. STBCi319-A (SFC199-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  5670. STBCi320-A (SFC031-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5671. STBCi324-A (SFC826-04-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  5672. STJUDEi004-A (INS3)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  5673. STJUDEi004-A-1 (INS3 Isogenic)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  5674. STJUDEi005-A (INS14)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  5675. STJUDEi005-A-1 (INS14 Isogenic)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  5676. STJUDEi007-A (PCS201)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Normal (average)

  5677. STJUDEi007-A-1 (2A5)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Samd9-associated hereditary myelodysplastic syndrome

  5678. STJUDEi007-A-2 (4H6)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Samd9-associated hereditary myelodysplastic syndrome

  5679. STJUDEi007-A-3 (3G10)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Samd9-associated hereditary myelodysplastic syndrome

  5680. STJUDEi007-A-4 (5B9)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Samd9-associated hereditary myelodysplastic syndrome

  5681. SUHi001-A (RES143 and Cell line 1 143)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5682. SUHi002-A (RES145 and Cell line 2 145)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5683. SUHi003-A (RES146 and Cell line 3 146)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5684. SUHi004-A (RES152 and cell line4 152)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Gastritis

  5685. SUHi005-A (RES165 and Cell line5 165)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5686. SUHi006-A (RES169 and Cell line6 169)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5687. SUHi007-A (RES102 and Cell line 7 102:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5688. SUHi008-A (Cell line 8 104:5 and RES104)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Asthma

  5689. SUHi009-A (RES105 and Cell line 12 105:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5690. SUHi010-A (RES117 and Cell line 9 117:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5691. SUHi011-A (RES151 and Cell line 13 151)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Asthma

  5692. SUHi012-A (RES163 and Cell line 14 163)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  5693. SUHi013-A (RES110 and Cell line 11 110:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5694. SUHi014-A (RES120 and Cell line 10 120:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Aortic dilatation

  5695. SUHi015-A (RES141 and Cell line 15 141)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5696. SUHi016-A (RES142 and Cell line 16 142:3)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5697. SUHi017-A (RES158 and Cell line 24 158)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Breast carcinoma

  5698. SUHi018-A (RES168 and Cell line 17 168)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Hypertension

  5699. SUHi020-A (RES114 and Cell line 19 114:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5700. SUHi021-A (RES116 and Cell line 20 116:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5701. SUHi022-A (RES118 and Cell line 21 118:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5702. SUHi023-A (RES121 and Cell line 22 121:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

    Disease:

    Type 2 diabetes mellitus

  5703. SUHi024-A (RES174 and Cell line 23 174)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  5704. SUSMi001-A (RY3)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Pelizaeus-merzbacher disease

  5705. SUSMi001-A-1 (128Lp1)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Pelizaeus-merzbacher disease

  5706. UCSFi001-A-64 (P633L RBM20 iPSCs)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Dilated cardiomyopathy

  5707. UCSFi001-A-65

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Dilated cardiomyopathy

  5708. SUSMi002-A (02-005)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Pelizaeus-merzbacher disease

  5709. SUSMi003-A (0524-1)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Normal (average)

  5710. SUSMi005-A

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  5711. SUSMi005-A-1 (SNCA3X 0KO C1 and SNCA3X 0KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  5712. SUSMi005-A-2 (SNCA3X 1KO C2 and SNCA3X 1KO C1)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  5713. SUSMi005-A-3 (SNCA3X 2KO C1 and SNCA3X 2KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  5714. SUSMi005-A-4 (SNCA3X 3KO C1 and SNCA3X 3KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  5715. SUSMi005-A-5 (SNCA3X 4KO C1 and SNCA3X 4KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  5716. SUTCMi001-A

    China Shandong University of Traditional Chinese Medicine (SUTCM)
    Disease:

    Normal (average)

  5717. SXMUi001-A (SXMUi002-A-1 and HB-iPSCs)

    China Shanxi Medical University (SXMU)
    Disease:

    Hemophilia b

  5718. SXMUi002-A (SXMUi001-A-1 and F8-iPSC)

    China Shanxi Medical University (SXMU)
    Disease:

    Hemophilia a

  5719. SYSUi002-A (CSFPhiPSC01.1)

    China Sun Yat-sen University (SYSU)
    Disease:

    Coronary slow flow phenomenon

  5720. SYSUi005-A

    China Sun Yat-sen University (SYSU)
    Disease:

    Hypertrophic cardiomyopathy

  5721. SYSUi007-A

    China Sun Yat-sen University (SYSU)
    Disease:

    Aicardi-goutieres syndrome

  5722. SYSUSCi001-A (CC-hiPSCs)

    China Sun Yat-Sen University, center for stem cell biology and tissue engineering (SYSUSC)
    Disease:

    Congenital cataract

  5723. SYSUSCi002-A (FNAIT-hiPSCs)

    China Sun Yat-Sen University, center for stem cell biology and tissue engineering (SYSUSC)
    Disease:

    Fetal and neonatal alloimmune thrombocytopenia

  5724. SYSUSCi004-A (IMO-hiPSCs)

    China Sun Yat-Sen University, center for stem cell biology and tissue engineering (SYSUSC)
    Disease:

    Autosomal recessive malignant osteopetrosis

  5725. SYSUTFi001-A

    China The First Affiliated Hospital (SYSUTF)
    Disease:

    Hepatocellular carcinoma

  5726. SZBKi001-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  5727. SZBKi001-B

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  5728. SZBKi002-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  5729. SZBKi002-B

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  5730. SZBKi003-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  5731. SZBKi004-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  5732. SZBKi005-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  5733. SZBKi006-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  5734. SZBKi006-B

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  5735. SZGJMSi001-A (ZLP-2)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Schizophrenia

  5736. SZGJMSi002-A (TSQ-1)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Obsessive-compulsive disorder

  5737. SZGJMSi003-A (TSH-2)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Normal (average)

  5738. SZGJMSi004-A (WJM-1)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Depression

  5739. TAUi001-A (UTA.09703.HCMJp)

    Finland Tampere University (TAU)
    Disease:

    Hypertrophic cardiomyopathy

  5740. TAUi001-A-1 (JPH2)

    Finland Tampere University (TAU)
    Disease:

    Hypertrophic cardiomyopathy

  5741. TAUi002-A (UTA.04602.WT)

    Finland Tampere University (TAU)
    Disease:

    Normal (average)

  5742. TAUi003-A (UTA.11505.WTsb)

    Finland Tampere University (TAU)
    Disease:

    Normal (average)

  5743. TAUi004-A (UTA.05208.CPVT)

    Finland Tampere University (TAU)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  5744. TAUi005-A (UTA.14511.CPVT)

    Finland Tampere University (TAU)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  5745. TAUi006-A (UTA.00102.LQT1)

    Finland Tampere University (TAU)
    Disease:

    Long qt syndrome 1

  5746. TAUi006-B (UTA.00118.LQT1)

    Finland Tampere University (TAU)
    Disease:

    Long qt syndrome 1

  5747. TAUi007-A (UTA.00208.LQT1)

    Finland Tampere University (TAU)
    Disease:

    Long qt syndrome 1

  5748. TAUi007-B (UTA.00211.LQT1)

    Finland Tampere University (TAU)
    Disease:

    Long qt syndrome 1

  5749. TAUi008-A (TAU2106C1.MS)

    Finland Tampere University (TAU)
    Disease:

    Multiple sclerosis

  5750. TCIERi001-A (IER-EK1)

    Taiwan Institute of Eye Research, Hualien Tzu Chi Hospital (TCIER)
    Disease:

    Normal (average)

  5751. TIGETi001-A (ND1.2)

    Italy San Raffaele Telethon Institute for Gene Therapy (SR-Tiget) (TIGET)
    Disease:

    Normal (average)

  5752. TIGETi003-A (GLD1.3)

    Italy San Raffaele Telethon Institute for Gene Therapy (SR-Tiget) (TIGET)
    Disease:

    Krabbe disease

  5753. TISSUi001-A (HUMIMIC101, StemUse101 and SU101)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  5754. TISSUi002-A (HUMIMIC102, StemUse102, SU102)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  5755. TISSUi003-A (HUMIMIC103, StemUse103, SU103)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  5756. TISSUi005-A (HUMIMIC105, StemUse105, SU105)

    Germany TissUse GmbH (TISSU)
    Disease:

    Leukemia

  5757. TISSUi006-A (HUMIMIC106, StemUse106 and SU106)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  5758. TISSUi007-A (HUMIMIC107, StemUse107 and SU107)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  5759. TMOi001-A (Gibco Episomal iPSC Line; A18945)

    United States Thermo Fisher Scientific (TMO)
    Disease:

    Normal (average)

  5760. TMPi001-A (K001 i6 and KO-001 i6)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5761. TMPi001-B (K001 i9, KO-001 i9, K001 c9 and KO-001 c9)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5762. TMPi002-A (K003 c14, K003 a14, KO-003 a14 and KO-003 c14)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5763. TMPi002-B (KO-003 a20, KO-003 c20, K003 c20 and K003 a20)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5764. TMPi003-A (KO-005 z12, K005 z12, KO-005 c12 and K005 c12)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5765. TMPi003-B (K005 z13, KO-005 c13, K005 c13 and KO-005 z13)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5766. TMPi004-A (K008 c13, KO-008 c13, K008 i13 and KO-008 i13)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5767. TMPi004-B (K008 c44, KO-008 c44, K008 i44 and KO-008 i44)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5768. TMPi005-A (K011 c6 and KO-011 c6)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5769. TMPi005-B (K011 c10 and KO-011 c10)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5770. TMPi006-A (MR-001 x3, MR001 x3, MR-001 c3 and MR001 c3)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5771. TMPi006-B (MR001 x15, MR-001 x15, MR-001 c15 and MR001 c15)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5772. TMPi007-A (MR-010 c3 and MR010 c3)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5773. TMPi007-B (MR-010 c18 and MR010 c18)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5774. TMPi008-A (MR-013 c3 and MR013 c3)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5775. TMPi008-B (MR-013 c13 and MR013 c13)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5776. 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

  5777. TMPi009-B (MR014 c27 and MR-014 c27)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5778. TMPi010-A (K013 c20 and KO-013 c20)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5779. TMPi010-B (K013 c39 and KO-013 c39)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5780. TMPi011-A (K015 c1 and KO-015 c1)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5781. TMPi011-B (K015 c9 and KO-015 c9)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  5782. TMPi012-A (MR-023 c17 and MR023 c17)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5783. TMPi012-B (MR023 c22 and MR-023 c22)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5784. TMPi013-A (MR-012 and MR012)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5785. TMPi013-B (MR-012 c12 and MR012 c12)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5786. TMPi014-A (MR030 c1 and MR-030 c1)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5787. TMPi014-B (MR030 c2 and MR-030 c2)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5788. TMPi015-A (NR-002 c2 and NR002 c2)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5789. TMPi015-B (NR002 c21 and NR-002 c21)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5790. TMPi016-A (NR003 c6 and NR-003 c6)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5791. TMPi016-B (NR003 c9 and NR-003 c9)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  5792. TNRMCi001-A (iTAF32)

    Russia Tomsk National Research Medical Center of the Russian Academy of Sciences (TNRMC)
    Disease:

    Cystic fibrosis

  5793. TONGJIi001-A (ZS15)

    China Tongji University (TONGJI)
    Disease:

    Infertility

  5794. TRDSi001-A (TRDS-Cardio-021)

    Israel Technion Research and Development Foundation (TRDS)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  5795. TRDSi002-A

    Israel Technion Research and Development Foundation (TRDS)
    Disease:

    Normal (average)

  5796. TRDSi002-A-1 (TRDS-Cardio-ArcLight)

    Israel Technion Research and Development Foundation (TRDS)
    Disease:

    Normal (average)

  5797. TRDSi004-A (TRDS-Cardio-012)

    Israel Technion Research and Development Foundation (TRDS)
    Disease:

    Long qt syndrome 2

  5798. TRNDi032-A (HT977A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Alagille syndrome

  5799. TRNDi033-A (HT1001-B)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Normal (average)

  5800. TRNDi034-A (HT1002-A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Normal (average)

  5801. TRNDi035-A (HT1004-B)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Normal (average)

  5802. TRNDi036-A (HT980A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Alagille syndrome

  5803. TRNDi037-A (HT976A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Alagille syndrome

  5804. TRNDi038-A (HT978A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Alagille syndrome

  5805. TRNDi042-A (HT528A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Mucopolysaccharidosis type iiib

  5806. TUMi001-A (C25)

    Germany Technische Universität München (TUM)
    Disease:

    Normal (average)

  5807. TUSMi001-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Normal (average)

  5808. TUSMi002-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Normal (average)

  5809. TUSMi003-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  5810. TUSMi004-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsessive-compulsive disorder

  5811. TUSMi005-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsolete_bipolar disorder

  5812. TUSMi006-A (15M0014)

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsolete_alzheimer's disease

  5813. TUSMi007-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  5814. TUSMi008-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  5815. TUSMi012-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Glioma

  5816. TUSMi013-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Parkinson disease

  5817. TUSMi014-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Parkinson disease

  5818. TYWHSTi002-A

    China Tianyou Hospital, Wuhan University of Science and Technology (TYWHST)
    Disease:

    Pendred syndrome

  5819. UAEUi001-A

    United Arab Emirates United Arab Emirates University (UAEU)
    Disease:

    Ventricular septal defect

  5820. UALGi003-A (BUB1P2-iPSC Cl1)

    Portugal Universidade do Algarve (UALG)

  5821. UALGi003-B (BUB1P2-iPSC Cl2)

    Portugal Universidade do Algarve (UALG)

  5822. UAMi001-A (PCCA23-FiPS4F8)

    Spain Universidad Autonoma de Madrid (UAM)
    Disease:

    Propionic acidemia

  5823. UAMi005-A

    Spain Universidad Autonoma de Madrid (UAM)
    Disease:

    Nonketotic hyperglycinemia

  5824. UAZTi009-A (MKAZ1)

    United States University of Arizona (UAZT)
    Disease:

    Normal (average)

  5825. UAZTi011-A (MKAZ3)

    United States University of Arizona (UAZT)
    Disease:

    Pontocerebellar hypoplasia type 1b

  5826. UBi001-A

    Spain University of Barcelona (UB)
    Disease:

    Normal (average)

  5827. UBi001-A-1

    Spain University of Barcelona (UB)
    Disease:

    Sanfilippo syndrome type c

  5828. UBi001-A-2

    Spain University of Barcelona (UB)
    Disease:

    Sanfilippo syndrome type c

  5829. UBi005-A (BJ_iPSC_SV4F_9)

    Spain University of Barcelona (UB)
    Disease:

    Normal (average)

  5830. UBCi002-A

    Canada University of British Columbia (UBC)
    Disease:

    Leukodystrophy, hypomyelinating, 22

  5831. UBGi001-A

    China uBriGene (Suzhou) Biosciences Co., Ltd. (UBG)
    Disease:

    Normal (average)

  5832. UBTi001-A (PEB-AL#6)

    Austria Medical University of Graz (UBT)
    Disease:

    Normal (average)

  5833. UBTi002-A (PEB-HM1 #3)

    Austria Medical University of Graz (UBT)
    Disease:

    Normal (average)

  5834. UBTi002-B (PEB-HM1 #5)

    Austria Medical University of Graz (UBT)
    Disease:

    Normal (average)

  5835. UBTi002-C (PEB-HM1 #8)

    Austria Medical University of Graz (UBT)
    Disease:

    Normal (average)

  5836. UCLi001-A (HHItC9S-V19)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  5837. UCLi002-A (HHItC9D-V34 and DN19)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  5838. UCLi003-A (TSM(exon10+16)V97)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  5839. UCLi004-A (RCi173 and RCFB60c6)

    United Kingdom University College London (UCL)
    Disease:

    Amyotrophic lateral sclerosis

    Disease:

    Frontotemporal dementia

  5840. UCLi004-B (RCFB60c7 and RCi177)

    United Kingdom University College London (UCL)
    Disease:

    Amyotrophic lateral sclerosis

    Disease:

    Frontotemporal dementia

  5841. UCLi004-C (RCi172 and RCFB60c2)

    United Kingdom University College London (UCL)
    Disease:

    Amyotrophic lateral sclerosis

    Disease:

    Frontotemporal dementia

  5842. UCLi005-A (LGMD2D Pt. 4 and LGMD2D #4)

    United Kingdom University College London (UCL)
    Disease:

    Limb-girdle muscular dystrophy

  5843. UCLi006-A (LCMD-L302P-UCL01C2)

    United Kingdom University College London (UCL)
    Disease:

    Congenital muscular dystrophy due to lmna mutation

  5844. UCLi009-A (CB1D)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  5845. UCLi009-B (CB1E)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  5846. UCLi010-A

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  5847. UCLi010-B (GL1B)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  5848. UCLi011-A

    United Kingdom University College London (UCL)
    Disease:

    Duchenne muscular dystrophy

  5849. UCLi012-A

    United Kingdom University College London (UCL)
    Disease:

    Duchenne muscular dystrophy

  5850. UCLi021-A (CLN5c.335G>A;619T>C and 484Pb)

    United Kingdom University College London (UCL)
    Disease:

    Cln5

  5851. UCLi022-A (546Pa and CLN5c.1072-1073delTT)

    United Kingdom University College London (UCL)
    Disease:

    Cln5

  5852. UCLi024-A (SMID277 and GOS111B)

    United Kingdom University College London (UCL)
    Disease:

    Argininosuccinic aciduria

  5853. UCLi026-A (UCL-NG-ADCY5-001)

    United Kingdom University College London (UCL)
    Disease:

    Dyskinesia with orofacial involvement, autosomal dominant

  5854. UCSCi001-A (SII-1802)

    Italy Università Cattolica del Sacro Cuore- Fondazione Policlinico Universitario "A. Gemelli" IRCCS (UCSC)
    Disease:

    Amyotrophic lateral sclerosis

  5855. 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

  5856. UCSDi001-A (UCSD182i-3-2 and iPSCORE_3_2)

    United States University of California,San Diego (UCSD)
    Disease:

    Normal (average)

  5857. 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

  5858. UCSDi001-A-2 (LQT3_35_iPSC_P15 and UCSD243i-LQT3-1)

    United States University of California,San Diego (UCSD)
    Disease:

    Long qt syndrome 3

  5859. 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

  5860. 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

  5861. 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

  5862. UCSFi001-A (wtc11, Wtc11, WTC, WTC11 and GM25256)

    United States Conklin Lab, Gladstone/UCSF (UCSF)
    Disease:

    Normal (average)

  5863. UCSFi002-A (BAG3-P209L)

    United States Conklin Lab, Gladstone/UCSF (UCSF)

  5864. UEFi004-A

    Finland University of Eastern Finland (UEF)
    Disease:

    Cstb wt allele

  5865. UEFi005-A (CO1)

    Finland University of Eastern Finland (UEF)
    Disease:

    Normal (average)

  5866. UEFi006-A (CO2)

    Finland University of Eastern Finland (UEF)
    Disease:

    Normal (average)

  5867. UEFi007-A (CO3)

    Finland University of Eastern Finland (UEF)
    Disease:

    Normal (average)

  5868. UEFi008-A (FTD1)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  5869. UEFi009-A (FTD2)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  5870. UEFi010-A (FTD3)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  5871. UEFi011-A (FTD4)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  5872. UEFi012-A (FTD5)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  5873. UEFi013-A (FTD6)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  5874. UGENTi001-A (UGENT-MFS003)

    Belgium Ghent University (UGENT)
    Disease:

    Marfan syndrome

  5875. UGENTi001-A-1 (UGENT-MFS003-CRISPR)

    Belgium Ghent University (UGENT)
    Disease:

    Marfan syndrome

  5876. UGENTi002-A

    Belgium Ghent University (UGENT)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  5877. UGENTi002-A-1

    Belgium Ghent University (UGENT)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  5878. UGENTi003-A (Clone_1 and EMC379i/c1)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  5879. UGENTi003-B (EMC379i/c3 and Clone_3)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  5880. UGENTi003-C (EMC379i/c4 and Clone_4)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  5881. UGENTi004-A (Clone_1 and EMC380i/c1)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  5882. UGENTi004-B (Clone_6 and EMC380i/c6)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  5883. UGENTi004-C (Clone_7 and EMC380i/c7)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  5884. UGENTi005-A (EMC368i/c1)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  5885. UGENTi005-B (EMC368i/c2)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  5886. UGENTi005-C (EMC368i/c6)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  5887. UGENTi006-A (EMC369i/c3)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  5888. UGENTi006-B (EMC369i/c8)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  5889. UGENTi006-C (EMC369i/c9)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  5890. UGENTi007-A (EMC370i/c4)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  5891. UGENTi007-B (EMC370i/c6)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  5892. UGENTi007-C (EMC370i/c14)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  5893. UGOTSAi002-B (N1-001iC2)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  5894. UGOTSAi003-A (N1-002iC3A)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  5895. UGOTSAi003-B (N1-002iC4)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  5896. UGOTSAi004-A (N1-003iC3)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  5897. UGOTSAi004-B (N1-003iC4)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  5898. UGOTSAi005-A (N1-004iC2)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Normal (average)

  5899. UGOTSAi005-B (N1-004iC6)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Normal (average)

  5900. UGOTSAi006-A (N1-005iC1)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  5901. UHi002-A (HEL13.1 and ALS50)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  5902. UHi003-A (ALS75 and HEL15.14)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  5903. UHi004-A (HEL157.1)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  5904. UHi004-B (HEL157.3)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  5905. UHi005-A (HEL158.1)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  5906. UHi005-B (HEL158.2)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  5907. UHi006-A (HEL24.3)

    Finland University of Helsinki (UH)
    Disease:

    Normal (average)

  5908. UHi006-A-1 (UHi001-A, HEL24.3-SOX2-nTdT-C9-H5 and HEL24.3-SOX2-nTdT)

    Finland University of Helsinki (UH)
    Disease:

    Normal (average)

  5909. UHi006-A-2 (HEL24.3-OCT4-nEmGFP-A-G3, UHi001-B and HEL24.3-OCT4-nEmGFP)

    Finland University of Helsinki (UH)
    Disease:

    Normal (average)

  5910. UHi006-A-3 (HEL24.3_IFIH1KO)

    Finland University of Helsinki (UH)
    Disease:

    Type i diabetes mellitus

  5911. UHi007-A (HEL47.2)

    Finland University of Helsinki (UH)
    Disease:

    Normal (average)

  5912. UHOMi001-A (iPCD02.30)

    France University Hospital of Montpellier (UHOM)
    Disease:

    Primary ciliary dyskinesia

  5913. UHOMi007-A (SMOK1)

    France University Hospital of Montpellier (UHOM)
    Disease:

    Normal (average)

  5914. UIOi001-A (AG27)

    Norway University of Oslo (UIO)
    Disease:

    Normal (average)

  5915. UIOi002-A (iPSC APOE3/3: Unaffected (Coriell #AG09173, female, Age 75))

    United States University of Oslo (UIO)

  5916. UIOi006-A (iPSC APOE4/4: Sporadic AD (Coriell #AG10788, female, Age 87))

    Norway University of Oslo (UIO)

  5917. UJNi001-A

    China University of Jinan (UJN)
    Disease:

    Cornelia de lange syndrome

  5918. UJSi001-A

    China Jiangsu University (UJS)
    Disease:

    Schizophrenia

  5919. UJSi003-A

    China Jiangsu University (UJS)
    Disease:

    Hereditary spastic paraplegia

  5920. UJSi004-A

    China Jiangsu University (UJS)
    Disease:

    Schizophrenia

  5921. UJSi005-A

    China Jiangsu University (UJS)
    Disease:

    Schizophrenia

  5922. UKAi001-A (iPS1 and hsc3_hiPS_11)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5923. UKAi001-A-1 (hsc3_hiPS_11_4 and IRF8-/- iPS1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5924. UKAi001-B (iPS2 and hsc3_hiPS_29)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5925. UKAi001-B-1 (hsc3_hiPS_29_23 and IRF8-/- iPS2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5926. UKAi001-C (hsc3_hiPS_40 and iPS3)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5927. UKAi001-C-1 (hsc3_hiPS_40_16_6 and IRF8-/- iPS3)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5928. UKAi002-A (PBMNC2_hiPS_007 and PV1 JAK2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  5929. UKAi002-A-1 (PV1 JAK2 : CXCL4 KO)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  5930. UKAi002-B (PBMNC2_hiPS_009 and PV1 JAK2 V617F het)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  5931. UKAi002-B-1 (PV1 JAK2 V617F het : CXCL4 KO)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  5932. UKAi003-A (hsc4_hiPS_021 and PV2 JAK2 V617F hom)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  5933. UKAi003-A-1 (PV2 JAK2 V617F het)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  5934. UKAi003-A-2 (PV2 JAK2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  5935. UKAi004-A (P4_wt4 and patient 1 control 1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5936. UKAi004-B (patient 1 control 2 and P4_wt8)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5937. UKAi004-C (P4_mut13 and patient 1 D816V 1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5938. UKAi004-D (P4_mut28 and patient 1 D816V 2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5939. UKAi004-E (P4_mut30 and patient 1 D816V 3)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5940. UKAi007-A (P13_wt5 and Patient 2 control 1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5941. UKAi007-B (P13_mut1 and Patient 2 D816V 1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5942. UKAi008-A (Patient 3 control 1 and P15_wt37)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5943. UKAi008-B (Patient 3 control 2 and P15_wt108)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5944. UKAi008-C (Patient 3 D816V 1 and P15_mut131)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  5945. UKAi009-A (BM 102-2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Normal (average)

  5946. UKAi010-A (BM 104-12)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Normal (average)

  5947. UKAi011-A (BM 106-3)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Normal (average)

  5948. UKBi001-B

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Machado-joseph disease

  5949. UKBi002-A (iLB-C2-36m-r2)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5950. UCSFi002-A-1

    Germany Universitätsklinikum Bonn (UKB)

  5951. UKBi003-A (iLB-MJD1-32m-r9 and LB-32-r9)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Machado-joseph disease

  5952. UKBi004-A (LB-30-12 and iLB-C1-30m-r12)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5953. UKBi005-A (iLB-C-31f-r1 and LB-31-1)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5954. UKBi006-A (iLB-C-35m-r1 and LB-35-1)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5955. UKBi007-A (LB-33-5 and iLB-MJD3-33f-r5)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Machado-joseph disease

  5956. UKBi008-A (iLB-MJD4-34m-r1 and LB-34-1)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Machado-joseph disease

  5957. UKBi010-A (iLB-DS-95f-r8)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Dravet syndrome

  5958. UKBi011-A (iLB-AD-169bm-s24)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Alzheimer disease

  5959. UKBi012-A (iLB-C-108bf-s3)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5960. UKBi013-A (iLB-C-133bm-s4)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5961. UKBi014-A (A-257s2)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Walker-warburg syndrome

  5962. UKBi015-A (iLB-C16bm-s6)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5963. UKBi015-A-6 (iLB-C16bm-s6 edit BAG3 E2)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  5964. UKBi015-A-7 (iLB-C16bm-s6 edit BAG3 E10)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  5965. UKBi015-A-8 (iLB-C16bm-s6 non-edit BAG3 E5)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  5966. UKBi015-B (iLB-C16bm-s16)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5967. UKBi015-B-1 (iLB-C16bm-s16 edit DNMT3A KO E11)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Clonal hematopoiesis of indeterminate potential

  5968. UKBi015-B-2 (iLB-C16bm-s16 edit EMILIN1 C1606T E9)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Aortic root aneurysm

  5969. UKBi015-B-3 (iLB-C16bm-s16 edit TET2 KO E1)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Clonal hematopoiesis of indeterminate potential

  5970. UKBi015-B-4 (iLB-C16bm-s16 edit MUC4 KO E8)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Bicuspid aortic valve

  5971. UKBi015-B-5 (iLB-C16bm-s16 edit AAVS1-doxCx43-E11 Hom)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5972. UKBi015-B-6 (iLB-C16bm-s16 edit AAVS1-dox-rEstus(ASAP-GTA)-E5 Hom)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5973. UKBi016-A (iLB-C107bm-s9)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5974. UKBi017-A (iLB-C14m-s11)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5975. UKBi018-A (iLB-C-106bf-s8)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5976. UKBi019-A (iLB-C89bf-s7)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5977. UKBi020-A (iLB-C-105bm-s4)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5978. UKBi021-A (iLB-C-109bm-s6)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  5979. UKBi022-A (iLB-BAG3-301bm-s2)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  5980. UKBi022-A-1 (iLB-BAG3-301bm-s2 BAG3 edit)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  5981. UKBi023-A (iLB-BAG3-P209L-313bm-s9)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  5982. UKBi023-A-1 (iLB-BAG3-P209L-313bm-s9 BAG3 edit)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  5983. UKEi001-A (ERC001sv1162)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  5984. UKEi001-A-1 (CRYABhom)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Desminopathy

  5985. UKEi001-A-2 (Biallelic NRAP-KO)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Cardiomyopathy

  5986. UKEi001-A-3 (NRAP-OE)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Cardiomyopathy

  5987. UKEi001-B (ERC001sv1352)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  5988. UKEi001-C (ERC001sv1355)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  5989. UKEi002-A (ERC017sv2575)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  5990. UKEi002-B (ERC017sv2576)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  5991. UKEi002-C (ERC017sv2596)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  5992. UKEi003-A (ERC018sv1583)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  5993. UKEi003-B (ERC018sv1590)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  5994. UKEi003-C (ERC018sv1634)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  5995. UKEi070-A (Het)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Hypertrophic cardiomyopathy

  5996. UKEi070-A-1 (Rep 28 and Iso Co)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Hypertrophic cardiomyopathy

  5997. UKEi070-A-2 (Bi-allelic mutant and Mut 103)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Hypertrophic cardiomyopathy

  5998. UKERi001-A (UKERiG3G-R1-047)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  5999. TMOi001-A-4 (SPG11_HA)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6000. UKERi002-A (UKERiM89-R1-006)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Obsolete_parkinson's disease

  6001. UKERi003-A (UKERiPX7-R1-001)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Obsolete_parkinson's disease

  6002. UKERi004-A (UKERi88H-R1-001)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Obsolete_parkinson's disease

  6003. UKERi005-A (UKERiO3H-R1-001)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6004. UKERi006-A (UKERi82A-R1-002)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6005. UKERi006-B (UKERi82A-S1-017)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6006. UKERi009-A (UKERi33Q-R2-006)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6007. UKERi010-A (UKERi7MN-S1-010)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6008. UKERi010-A-1 (UKERi7MN-010-1)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6009. UKERi010-A-2 (UKERi7MN-010-2)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal (average)

  6010. UKHGi001-A (M-PKE (c))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Normal (average)

  6011. DPEDi001-A-1

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Atrial fibrillation

  6012. UKHGi001-B (M-PKE (e))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Normal (average)

  6013. UKHGi002-A (F-PKE (2))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Normal (average)

  6014. UKHGi002-B (F-PKE (3))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Normal (average)

  6015. UKHGi003-A (PKE (C))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Autism spectrum disorder

    Disease:

    Intellectual disability

  6016. UKHGi003-B (PKE (D))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Autism spectrum disorder

    Disease:

    Intellectual disability

  6017. MRIi016-A-1 (SHOX2 c.*28T>C_isoWT)

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Atrial fibrillation

  6018. MRIi016-A-2

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Atrial fibrillation

  6019. UKJi001-A (PKP2-hiPSC)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Normal (average)

  6020. UKJi003-A (hiPSC-FD)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Fabry disease

  6021. UKJi004-A (hiPSC-WT)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Normal (average)

  6022. UKJi005-A (hiPSC-FS.2)

    Germany Universitätsklinikum Jena (UKJ), Klinik für Innere Medizin I (KIM I), Dr. M. Bekhite ELsaied (UKJ)
    Disease:

    Normal (average)

  6023. 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

  6024. UKKi006-A (D4-cB, M4C4 and NP0053-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6025. UKKi007-A (NP0014-6 and UKK007Ai)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  6026. UKKi007-B (NP0014-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  6027. UKKi008-A (NP0016-3)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6028. UKKi009-A (NP0011-8)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6029. UKKi009-B (NP0011-19)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6030. UKKi011-A (NP0040-8)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6031. UKKi012-A (NP0041-17 and NP0041)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6032. UKKi016-A (NP0078-10)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6033. UKKi016-B (NP0078-12)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6034. UKKi016-C (NP0078-13)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6035. UKKi017-A (NP0075-8D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6036. UKKi017-B (NP0075-10K)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6037. UKKi017-C (NP0075-11B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6038. UKKi018-A (NP0080-2B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6039. UKKi018-B (NP0080-6A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6040. UKKi018-C (NP0080-8B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6041. UKKi019-A (NP0081-1A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6042. UKKi019-B (NP0081-11)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6043. UKKi019-C (NP0081-12C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6044. UKKi020-A (NP0100-4)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6045. UKKi020-B (NP0100-8)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6046. UKKi020-C (NP0100-10E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6047. UKKi020-D (NP0100-11)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6048. UKKi021-A (NP0105-2)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6049. UKKi021-B (NP0105-19)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6050. UKKi022-A (NP0106-34)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6051. UKKi022-C (NP0106-10A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6052. UKKi022-D (NP0106-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6053. UKKi023-A (NP0126-1)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6054. UKKi023-B (NP0126-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6055. UKKi023-C (NP0126-6)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6056. UKKi024-A (NP0133-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6057. UKKi024-B (NP0133-1)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6058. UKKi024-C (NP0133-4)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6059. UKKi025-A (NP0135-1)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6060. UKKi025-B (NP0135-2)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6061. UKKi025-C (NP0135-7)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6062. UKKi026-A (NP0114-1A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6063. UKKi026-B (NP0114-2C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6064. UKKi026-C (NP0114-5E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6065. UKKi027-A (NP0101-A and NP0101-3D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6066. UKKi027-B (NP0101-B and NP0101-4C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6067. UKKi027-C (NP0101-C and NP0101-10H)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6068. UKKi028-A (NP0115-A and NP0115-4)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6069. UKKi028-B (NP0115-B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6070. UKKi028-C (NP0115-C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6071. UKKi029-A (NP0077-6D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6072. UKKi029-B (NP0077-16E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6073. UKKi029-C (NP0077-18C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6074. UKKi030-A (NP0134-6D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6075. UKKi030-B (NP0134-18A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6076. UKKi030-C (NP0134-26B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  6077. UKKi031-A (NP0138-8B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6078. UKKi031-B (NP0138-19E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6079. UKKi031-C (NP0138-31B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6080. UKKi032-A (NP0141-12C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6081. UKKi032-B (NP0141-17A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6082. UKKi032-C (NP0141-31B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6083. UKKi034-A (NP0079-A and NP0079-7B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6084. UKKi034-B (NP0079-B and NP0079-15B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6085. UKKi034-C (NP0079-C and NP0079-16H)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  6086. UKKi035-A (NP0139-A and NP0139-3E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6087. UKKi035-B (NP0139-B and NP0139-6C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6088. UKKi035-C (NP0139-C and NP0139-24D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  6089. UKKi036-A (NP0143-A and NP0143-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6090. UKKi036-B (NP0143-B and NP0143-15)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6091. UKKi036-C (NP0143-C and NP0143-18)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6092. UKKi037-A (NP0144-A and NP0144-32)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6093. UKKi037-B (NP0144-B and NP0144-33)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6094. UKKi037-C (NP0144-C and NP0144-41)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  6095. UKMi003-A

    Germany University Hospital Muenster (UKM)
    Disease:

    Sinus bradycardia

  6096. UKMi004-A

    Germany University Hospital Muenster (UKM)
    Disease:

    Normal (average)

  6097. UKMi005-A

    Germany University Hospital Muenster (UKM)
    Disease:

    Sinus node dysfunction

  6098. UKMi009-A (HCN4 K1 homo)

    Germany University Hospital Muenster (UKM)
    Disease:

    Sick sinus syndrome

  6099. UKMi011-A (HCN4 K1 hetero)

    Germany University Hospital Muenster (UKM)
    Disease:

    Sick sinus syndrome

  6100. UKWi008-A (PARK2-9 CL12)

    Germany Universitätsklinikum Würzburg (UKW)
    Disease:

    Attention deficit-hyperactivity disorder

  6101. UKWi008-A-1 (PARK2-9 CL22)

    Germany Universitätsklinikum Würzburg (UKW)
    Disease:

    Attention deficit-hyperactivity disorder

  6102. UKWi009-A (SK310 CL1)

    Germany Universitätsklinikum Würzburg (UKW)
    Disease:

    Normal (average)

  6103. UKWi009-A-1 (SK310 CL5)

    Germany Universitätsklinikum Würzburg (UKW)
    Disease:

    Normal (average)

  6104. UKWMPi001-A

    Germany Division of Molecular Psychiatry, Center of Mental Health (UKWMP)
    Disease:

    Normal (average)

  6105. UKWNLi006-A (GLA-D170N-iPSC-1, FD1089/20 and GLA-508G>A-1)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6106. UKWNLi006-B (GLA-D170N-iPSC-2, GLA-508G>A-2 and FD1089/21)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6107. UKWNLi007-A (GLA-515G>A-1, GLA-C172Y-iPSC-1 and FD1210/1)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6108. UKWNLi007-B (GLA-515-G>A-2, FD1210/2 and GLA-C172Y-iPSC-2)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6109. UKWNLi008-A (SFN 1097_2)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Small fiber neuropathy

  6110. UKWNLi008-B (SFN 1097_3)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Small fiber neuropathy

  6111. UKWNLi008-C (SFN 1097_5)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Small fiber neuropathy

  6112. UKWNLi009-A (TK8, FD-1 and FD_1052)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6113. UKWNLi009-A-1 (IsoTK8 and IsoFD-1)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  6114. UKWNLi010-A (Bi093 Cl1)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  6115. UKWNLi010-B (Bi093 Cl5)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  6116. UKWNLi010-C (Bi093 Cl8)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Chemotherapy-induced peripheral neuropathy

  6117. ULBi002-A (Hel115.6)

    Belgium Université Libre de Bruxelles (ULB)
    Disease:

    Normal (average)

  6118. ULBi003-A (HEL46.11)

    Belgium Université Libre de Bruxelles (ULB)
    Disease:

    Normal (average)

  6119. ULBi004-A (AH4)

    Belgium Université Libre de Bruxelles (ULB)
    Disease:

    Normal (average)

  6120. ULEIi001-A

    Germany Leipzig University (ULEI)
    Disease:

    Normal (average)

  6121. 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

  6122. 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

  6123. 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

  6124. UMi035-A (GM07968)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Gaucher disease type 1

  6125. UMi036-A (ND34263)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Parkinson disease

  6126. UMi038-A

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer disease

  6127. UMi038-A-1

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer disease

  6128. UMi039-A

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6129. UMi039-A-1

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6130. UMi040-A (SB162-284 cl.1)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Auditory neuropathy spectrum disorder

  6131. UMi041-A (410730)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6132. UMi042-A

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6133. UMi042-A-1 (408737 CB9)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6134. UMi043-A (AD 381852 clone #1)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  6135. UMi044-A (**1113.4)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Charcot-marie-tooth disease type 4b3

  6136. UMi045-A (**1159.1)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Charcot-marie-tooth disease type 4b3

  6137. UMi046-A (***1407.3)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Charcot-marie-tooth disease type 4b3

  6138. UMi047-A (sord1 DM)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy

  6139. UMi048-A (sord1 GB)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy

  6140. UMi049-A (IIsord1 RV)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy

  6141. UMi050-A (417027 clone 8)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer disease

  6142. UMi050-B (417027 clone 3)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer disease

  6143. UMi052-A (PLS405757 Cl#3)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Primary lateral sclerosis

  6144. UMi053-A (PLS405714 Cl#4)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Primary lateral sclerosis

  6145. UMANi255-A (NB221c)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Foveal hypoplasia

  6146. UMANi255-A-1 (PS02b-B6)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Foveal hypoplasia

  6147. UMANi257-A (AGD-14-01)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Cadasil

  6148. UMANi258-A (AGD-14-04)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Cadasil

  6149. UMANCi001-A (TF173B)

    United Kingdom C2T-Kimber lab (UMANC)
    Disease:

    Normal (average)

  6150. UMANCi002-A (TF172D)

    United Kingdom C2T-Kimber lab (UMANC)
    Disease:

    Hnf1b

  6151. UMANCi003-A (TF171A)

    United Kingdom C2T-Kimber lab (UMANC)
    Disease:

    Hnf1b

  6152. UMCGi001-A (PPCM RC1 c1)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6153. UMCGi001-B (PPCM RC1 c2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6154. UMCGi002-A (CTP1-C1)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Cardiomyopathy

  6155. UMCGi002-B (CTP1-C2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Cardiomyopathy

  6156. UMCGi002-C (CTP1-C3)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Cardiomyopathy

  6157. UMCGi003-A (PPCM RP1 c1)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Peripartum cardiomyopathy

  6158. UMCGi003-B (PPCM RP1 c3)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Peripartum cardiomyopathy

  6159. UMCGi004-A (PPCM RC2 c1)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6160. UMCGi004-B (PPCM RC2 c2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6161. UMCGi005-A (PPCM RP2 c2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Peripartum cardiomyopathy

  6162. UMCGi005-B (PPCM RP2 c9)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Peripartum cardiomyopathy

  6163. UMCGi006-A (DRP1-C2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6164. UMCGi006-B (DRP1-C3)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6165. UMCGi007-A (DRP2-C2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6166. UMCGi007-B (DRP2-C4)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6167. UMCGi008-A (DRP3-C5)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6168. UMCGi008-B (DRP3-C7)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6169. UMCGi008-C (DRP3-C10)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6170. UMCGi008-D (DRP3-C11)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  6171. UMCGi009-A (PLN2-C2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Cardiomyopathy

  6172. UMCGi011-A (CTP2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  6173. UMCGi011-B (CTP2-C5)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  6174. UMCGi011-C (CTP2-C4)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  6175. UMCGi012-A (UMCG-PD-iPSC-T369M)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Parkinson disease

  6176. UMCGi013-A (UMCG-PD-iPSC-E326K)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Parkinson disease

  6177. UMCGi014-A (UMCG-PD-iPSC-nonGBA1/A)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Parkinson disease

  6178. UMCGi015-A (UMCG-PD-iPSC-nonGBA1/B)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Parkinson disease

  6179. UMCGi016-A (CTP3-C3)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  6180. UMCGi016-B

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  6181. UMCUi001-A (CRYAB-A527G-11C1)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Dilated cardiomyopathy 1ii

  6182. UMCUi002-A (CRYAB-A527G-12C6)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Dilated cardiomyopathy 1ii

  6183. UMCUi003-A (CRYAB-A527G-91C10)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Dilated cardiomyopathy 1ii

  6184. UMCUi004-A (CRYAB-A527G-92C25)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6185. UMCUi005-A (aPLN-R14del-GR04C1)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Cardiomyopathy

  6186. UMCUi006-A (PLN-GR05C5)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6187. UMCUi007-A (84C12)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Aortic dissection

  6188. UMCUi008-A (86C6)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Aortic root aneurysm

  6189. UMCUi009-A (87C3)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6190. UMCUi010-A (88C6)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6191. UMCUi011-A (119C9)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Aortic root aneurysm

  6192. UMCUi012-A (aPLN-R14del-GR02C8)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Cardiomyopathy

  6193. UMCUi013-A (TNNI3 P1C26)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Restrictive cardiomyopathy

  6194. UMCUi014-A (TNNI3 P2C27)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Restrictive cardiomyopathy

  6195. UMCUi015-A (TNNI3 C1C1)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6196. UMCUi016-A (TNNI3 C2C14)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  6197. RUCDRi002-A-73 (IPSC-CraCCER and LiPSC-GR1.1-CraCCER, TC-1133-CraCCER)

    Germany University Medical Center Goettingen (UMG)
    Disease:

    Normal (average)

  6198. 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)

  6199. UMGACBi001-A

    Germany Institute of Anatomy and Cell Biology (UMGACB)

  6200. MHHi001-A-12 (Phx_SRCAP_g3_1200_4)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  6201. MHHi001-A-13 (Phx_SRCAP_g3_1200_7)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  6202. 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

  6203. 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

  6204. 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

  6205. UMGWi001-B (Z1 K3v3)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Floating-harbor syndrome

  6206. UMGWi004-A (BNH1 _iPSC_WT_8)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  6207. UMGWi004-B (BNH1 _iPSC_WT_48)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  6208. UMGWi004-B-1 (BNH1_iPSC_FHS1_cr_well7_JR)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Floating-harbor syndrome

  6209. UMGWi004-B-2 (BNH1_iPSC_FHS1_cr_well12_JR)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Floating-harbor syndrome

  6210. UMICHi001-A (HVRDi004-B, GM23338 and PGP1 Parental)

    United States University of Michigan (UMICH)
    Disease:

    Normal (average)

  6211. UMICHi001-A-1 (ITPR1 Wildtype and UMICHi001-AB)

    United States University of Michigan (UMICH)
    Disease:

    Normal (average)

  6212. UMICHi001-A-2 (ITPR1 Het and ITPR1+/-)

    United States University of Michigan (UMICH)
    Disease:

    Spinocerebellar ataxia type 15/16

  6213. UMILi001-A (KAB07)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  6214. UMILi002-A (KAB01)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  6215. UMILi003-A (KAB03)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  6216. UMILi004-A (KAB04)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  6217. UMILi005-A (KAB05)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  6218. UMILi006-A (CTL05)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6219. UMILi007-A (CTL06)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6220. UMILi008-A (CTL07)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6221. UMILi009-A (GAD02)

    Italy University of Milan (UMIL)
    Disease:

    Gabriele-de vries syndrome

  6222. UMILi010-A (GAD01)

    Italy University of Milan (UMIL)
    Disease:

    Gabriele-de vries syndrome

  6223. UMILi011-A (CTL10)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6224. UMILi012-A (WVS02)

    Italy University of Milan (UMIL)
    Disease:

    Weaver syndrome

  6225. UMILi013-A (WVS01)

    Italy University of Milan (UMIL)
    Disease:

    Weaver syndrome

  6226. UMILi014-A (WVS04)

    Italy University of Milan (UMIL)
    Disease:

    Weaver syndrome

  6227. UMILi015-A (WVS03)

    Italy University of Milan (UMIL)
    Disease:

    Weaver syndrome

  6228. UMILi016-A (DUP01)

    Italy University of Milan (UMIL)
    Disease:

    7q11.23 microduplication syndrome

  6229. UMILi017-A (DUP02)

    Italy University of Milan (UMIL)
    Disease:

    7q11.23 microduplication syndrome

  6230. UMILi018-A (DUP03)

    Italy University of Milan (UMIL)
    Disease:

    7q11.23 microduplication syndrome

  6231. UMILi019-A (DUP04)

    Italy University of Milan (UMIL)
    Disease:

    7q11.23 microduplication syndrome

  6232. UMILi020-A (WBS04)

    Italy University of Milan (UMIL)
    Disease:

    Williams-beuren syndrome

  6233. UMILi021-A (WBS03)

    Italy University of Milan (UMIL)
    Disease:

    Williams-beuren syndrome

  6234. UMILi022-A (WBS01)

    Italy University of Milan (UMIL)
    Disease:

    Williams-beuren syndrome

  6235. UMILi023-A (WBS02)

    Italy University of Milan (UMIL)
    Disease:

    Williams-beuren syndrome

  6236. UMILi024-A (CTL04)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6237. UMILi025-A (CTL09)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6238. UMILi026-A (CTL01)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  6239. UMILi027-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6240. UMILi028-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6241. UMILi032-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6242. UMILi033-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6243. UMILi034-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6244. UMILi035-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6245. UMILi036-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  6246. UMNi001-A (iPSC LUCAS1)

    United States University of Minnesota (UMN)
    Disease:

    Normal (average)

  6247. UNAMi001-A (IFC-UNAM iPD01-S)

    Mexico Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)
    Disease:

    Parkinson disease

  6248. UNAMi002-A (IFC-UNAM iPD02-S)

    Mexico Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)
    Disease:

    Parkinson disease

  6249. UNAMi003-A (IFC-UNAM iPD03-PINK1)

    Mexico Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)
    Disease:

    Parkinson disease

  6250. UNEWi001-A (UNEW001Ai)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6251. UNEWi002-A (UNEW002Ai and PRPF31 AW)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6252. UNEWi003-A (PRPF31-HD)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6253. UNEWi004-A (PRPF31 SH)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6254. UNEWi005-A (PRPF31 RH)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6255. UNEWi006-A

    United Kingdom University of Newcastle (UNEW)

  6256. UNEWi011-A (UNEW011Ai)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Cernunnos-xlf deficiency

  6257. UNEWi017-A

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Aplastic anemia

  6258. UNEWi018-A

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Aplastic anemia

  6259. UNEWi019-A

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Anemia

  6260. UNEWi021-A (F018 13.2)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6261. UNEWi021-B (F018 15.8)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6262. UNEWi021-C (F018 17/8-1)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6263. UNEWi022-A (F181 5.8)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6264. UNEWi022-B (F181 18.2)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6265. UNEWi022-C (F181 25.7)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6266. UNEWi023-A (F343 clone 2)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6267. UNEWi023-B (F343 clone 3)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6268. UNEWi023-C (F343 clone 4)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6269. UNEWi024-A (F180-1)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6270. UNEWi024-B (F180-2)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6271. UNEWi024-C (F180-3)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6272. UNEWi025-A (F324 5.8)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6273. UNEWi025-B (F324 12.8)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6274. UNEWi025-C (F324 19.7)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  6275. UNEWi026-A (SF116 clone 1)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Age-related macular degeneration

  6276. UNEWi026-B (SF116 clone 2)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Age-related macular degeneration

  6277. UNEWi026-C (SF116 clone K)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Age-related macular degeneration

  6278. UNEWi027-A (F116)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Retinitis pigmentosa

  6279. UNIBSi017-A (EDS-iPSC)

    Italy University of Brescia (UNIBS)

  6280. UNIBSi018-A

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6281. UNIBSi018-B

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6282. UNIBSi019-A

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6283. UNIBSi019-B

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6284. UNIBSi020-A

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6285. UNIBSi020-B

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  6286. UNIFEi001-A (iPSca1N1, MARPiPSCA1N1 and UniFei001-A)

    Italy University of Ferrara (UNIFE)
    Disease:

    Spinocerebellar ataxia type 1

  6287. UNIFEi002-A (UNIFEi013-A, UniFei013-A, MARPiPSCA1N13 and iPSca1N13)

    Italy University of Ferrara (UNIFE)
    Disease:

    Spinocerebellar ataxia type 1

  6288. UNIMGi009-A (PD-1M)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Parkinson disease

  6289. UNIMGi010-A (PD-4F)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Parkinson disease

  6290. UNIMGi011-A (PD-2M)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Parkinson disease

  6291. UNIMGi012-A (PRICKLE2 MUTmild)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Epilepsy syndrome

  6292. UNIMGi013-A (PRICKLE2 MUTsevere)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Epilepsy syndrome

  6293. UNIONi001-A (UNION-ViPS-C2401022)

    China UNION STEM CELL & GENE ENGINEERING CO., LTD. (UNION)
    Disease:

    Normal (average)

  6294. UNIPDi004-A

    Italy University of Padova (UNIPD)
    Disease:

    Normal (average)

  6295. UNIPDi004-B (HDP04)

    Italy University of Padova (UNIPD)
    Disease:

    Normal (average)

  6296. UNIPDi005-A

    Italy University of Padova (UNIPD)
    Disease:

    Normal (average)

  6297. UNIPDi006-A

    Italy University of Padova (UNIPD)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  6298. UNIPDi008-A (FXS-GM05131)

    Italy University of Padova (UNIPD)
    Disease:

    Fragile x syndrome

  6299. UNIPDi008-B (FXS GM05131 primed)

    Italy University of Padova (UNIPD)
    Disease:

    Fragile x syndrome

  6300. UNIPDi009-A

    Italy University of Padova (UNIPD)
    Disease:

    Fragile x syndrome

  6301. UNIPDi010-B (Primed-555 FRX)

    Italy University of Padova (UNIPD)
    Disease:

    Fragile x syndrome

  6302. UNIPVi001-A (COR248 and NG2409)

    Italy Units of Biology and Genetics - University of Pavia (UNIPV)
    Disease:

    Joubert syndrome

  6303. UNIPVi002-A (HDF108)

    Italy Units of Biology and Genetics - University of Pavia (UNIPV)
    Disease:

    Normal (average)

  6304. UNIPVi003-A (HDF109)

    Italy Units of Biology and Genetics - University of Pavia (UNIPV)
    Disease:

    Normal (average)

  6305. UNIPVi004-A (COR316 and NG3157)

    Italy Units of Biology and Genetics - University of Pavia (UNIPV)
    Disease:

    Joubert syndrome

  6306. UNIZARi001-A (FiPSTK2-2)

    Spain University of Zaragoza (UNIZAR)
    Disease:

    Mitochondrial dna depletion syndrome, myopathic form

  6307. UOCi001-A (CIM001.4)

    Australia University of Calgary (UOC)

  6308. UOCi002-A (CIM008.6)

    Australia University of Calgary (UOC)

  6309. UOCi003-A (GPiPSC 31-1)

    Canada University of Calgary (UOC)
    Disease:

    Simplified gyral pattern

  6310. UOCi003-A-1 (A18 GPiPSC 31-1)

    Canada University of Calgary (UOC)
    Disease:

    Simplified gyral pattern

  6311. UOCi004-A

    Canada University of Calgary (UOC)
    Disease:

    Spondylocostal dysostosis

  6312. UOCi005-A

    Canada University of Calgary (UOC)
    Disease:

    Anencephaly

  6313. UODi001-A (ChiPS4 and ChiPSC4)

    United Kingdom University of Dundee (UOD)
    Disease:

    Normal (average)

  6314. UOFTi001-A (CT002)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6315. UOFTi003-A (CT004)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6316. UOFTi004-A (BD001)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6317. UOFTi005-A (BD002)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6318. UOFTi006-A (BD003)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6319. UOFTi007-A (MS002)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6320. UOFTi008-A (MS004)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6321. UOFTi009-A (MS012)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  6322. UOFTi010-A (MS015)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

    Disease:

    Mitochondrial disease

  6323. UOFTi011-A (MS003)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6324. UOFTi012-A (MS006)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6325. UOFTi013-A (MS008)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6326. UOFTi014-A (MS009)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6327. UOFTi015-A (MS010)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  6328. UOHi002-A (UOHi002 with its alternative name as UOHi002SHANK3)

    Israel University of Haifa (UOH)
    Disease:

    Normal (average)

  6329. UOHi003-A (UOHi001 with its alternative name as UOHi001SHANK3)

    Israel University of Haifa (UOH)
    Disease:

    Phelan-mcdermid syndrome

  6330. UOMi008-A (ACS-hiPSC-HPP2)

    Canada University of Manitoba (UOM)
    Disease:

    Hypophosphatasia

  6331. UOMi009-A (ACS-hiPSC-HPP3)

    Canada University of Manitoba (UOM)
    Disease:

    Hypophosphatasia

  6332. UOMi010-A (ANCS-hiPSC-HPP5)

    Canada University of Manitoba (UOM)
    Disease:

    Hypophosphatasia

  6333. UOMi011-A (ANCS-hiPSC-HPP6)

    Canada University of Manitoba (UOM)
    Disease:

    Hypophosphatasia

  6334. UOMi012-A (NAAS-hiPSC-Fontan1)

    Canada University of Manitoba (UOM)
    Disease:

    Fontan procedure

  6335. UOSi001-A (MIFF1, ShiPS-MIFF1 and MIFF-1)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  6336. UOSi001-B (MIFF3, MIFF-3 and ShiPS-MIFF3)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  6337. UTSWi001-A-2 (FA1-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6338. UTSWi001-A-3 (FA1ic-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6339. UTSWi002-A-2 (FA2-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6340. UTSWi002-A-3 (FA2ic-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6341. UTSWi003-A-2 (FA3-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6342. UTSWi003-A-3 (FA3ic-N)

    Australia University of Wollongong (UOW)
    Disease:

    Friedreich ataxia

  6343. UOXFi001-A (MK071-1)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6344. UOXFi001-B (MK071-3)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6345. UOXFi001-C (MK071-5)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6346. UOXFi001-D (MK071-6)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6347. UOXFi002-A (MK082-26)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6348. UOXFi002-B (MK082-30)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6349. UOXFi003-A (MK088-1)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6350. UOXFi003-C (MK088-7)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6351. UOXFi004-A (OX1-18)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6352. UOXFi004-B (OX1-19)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6353. UOXFi005-A (JR053-1 and SAMEA4453899)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6354. UOXFi005-B (JR053-6)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6355. UOXFi006-A (OX2-28)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6356. UOXFi007-A (MK002-4)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6357. UOXFi007-B (MK002-6)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6358. UOXFi007-C (MK002-7)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6359. UOXFi008-A (MK144-1)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6360. UOXFi008-B (MK144-7)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6361. UOXFi008-C (MK144-10)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6362. UOXFi009-A (MK024-3)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6363. UOXFi009-B (MK024-4)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6364. UOXFi009-C (MK024-9)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6365. UOXFi010-A (JR023-1)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6366. UOXFi010-B (JR023-2)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6367. UOXFi010-C (JR023-5)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6368. UOXFi010-D (JR023-7)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6369. STBCi063-A-1 (SFC856-03-04 PINK1-/-A12)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6370. STBCi063-A-2 (SFC856-03-04 STING-/-F11D1)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  6371. STBCi324-A-1 (SFC826-04-06 STING-/-B12)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  6372. UPITTi004-A (CN090 C5A5J2)

    United States University of Pittsburgh (UPITT)
    Disease:

    Sickle cell anemia

  6373. UPITTi004-B (CN090 C1B5B5)

    United States University of Pittsburgh (UPITT)
    Disease:

    Sickle cell anemia

  6374. UPITTi005-A (MAGE112_Clone16)

    United States University of Pittsburgh (UPITT)
    Disease:

    Sickle cell anemia

  6375. UPITTi005-B (MAGE112_Clone17)

    United States University of Pittsburgh (UPITT)
    Disease:

    Sickle cell anemia

  6376. UPSFRi001-A (PB03)

    France Université Paris-Sud 11 (UPSFR)

  6377. UPSFRi002-A (PB04)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Beta thalassemia

  6378. UPSFRi003-A (PB05-1)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Beta thalassemia

  6379. UPSFRi004-A (PB05)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Beta thalassemia

  6380. UPSFRi004-A-1 (PB05-1)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Beta thalassemia

  6381. UPSFRi005-A (PB06)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Down syndrome

  6382. UPSFRi005-A-1 (PB06-1)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Down syndrome

  6383. UPSFRi006-A (PB07)

    France Université Paris-Sud 11 (UPSFR)

  6384. UPSFRi007-A (PB08)

    France Université Paris-Sud 11 (UPSFR)

  6385. UPSFRi008-A (PB09)

    France Université Paris-Sud 11 (UPSFR)

  6386. UPSFRi009-A (PB10)

    France Université Paris-Sud 11 (UPSFR)

  6387. UQi001-A (C11-WT)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6388. UQi001-A-1 (C11-TDP43-A382T)

    Australia The University of Queensland (UQ)
    Disease:

    Amyotrophic lateral sclerosis

  6389. UCSFi001-A-1O (dPRO)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6390. UCSFi001-A-1P (dLAMA)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6391. UCSFi001-A-1Q (dGFP)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6392. UQi002-A (C3)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6393. UQi003-A (C7)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6394. UQi004-A (C12)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6395. UQi005-A (C13)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  6396. UQi006-A (M2)

    Australia The University of Queensland (UQ)
    Disease:

    Amyotrophic lateral sclerosis

  6397. UQi007-A (M4)

    Australia The University of Queensland (UQ)
    Disease:

    Amyotrophic lateral sclerosis

  6398. UQi008-A (M8)

    Australia The University of Queensland (UQ)
    Disease:

    Amyotrophic lateral sclerosis

  6399. UQi009-A (M15)

    Australia The University of Queensland (UQ)
    Disease:

    Amyotrophic lateral sclerosis

  6400. UQACi001-A (iPSC-EBS21)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6401. UQACi002-A (iPSC-EBS1)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6402. UQACi003-A (iPSC-EBS2)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6403. UQACi004-A (iPSC-EBS9)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6404. UQACi005-A (iPSC-EBS10)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6405. UQACi006-A (iPSC-EBS26)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6406. UQACi007-A (iPSC-EBS29)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  6407. URi001-A

    Japan University of the Ryukyus (UR)
    Disease:

    Major depressive disorder

  6408. URi002-A

    Japan University of the Ryukyus (UR)
    Disease:

    Bipolar disorder

  6409. URi004-A

    Japan University of the Ryukyus (UR)
    Disease:

    Normal (average)

  6410. URi005-A

    Japan University of the Ryukyus (UR)
    Disease:

    Bipolar disorder

  6411. USCBi001-A (NIBSC_i008, NIBSC8,)

    United Kingdom National Institute for Biological Standards and Control - UK Stem Cell Bank (USCB)
    Disease:

    Normal (average)

  6412. USFi001-A (1CN1.5)

    United States University of South Florida (USF)
    Disease:

    Friedreich ataxia

  6413. USFi002-A (0AS1)

    United States University of South Florida (USF)
    Disease:

    Dilated cardiomyopathy

  6414. USFi003-A (1AB1)

    United States University of South Florida (USF)
    Disease:

    Dilated cardiomyopathy

  6415. USFi004-A (3IV6)

    United States University of South Florida (USF)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  6416. USFi005-A (CUUSFi001-A and LQT1)

    United States University of South Florida (USF)

  6417. USFi006-A (CUUSFi002-A and LQT2)

    United States University of South Florida (USF)
    Disease:

    Normal (average)

  6418. USFi007-A (CUUSFi003-A and LQT3)

    United States University of South Florida (USF)
    Disease:

    Normal (average)

  6419. USPi001-A (iPS_LGH_AHDC1_P1)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Xia-gibbs syndrome

  6420. USPi002-A (iPS_LGH_AHDC1_P2)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Xia-gibbs syndrome

  6421. USPi003-A (iPS_LGH_AHDC1_P3)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Xia-gibbs syndrome

  6422. USPi004-A (DFNA58-ipsc-con1-cl4)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Normal (average)

  6423. USPi005-A (DFNA58-ipsc-con2-cl1)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Normal (average)

  6424. USPi006-A (DFNA58-ipsc-dup1-cl2)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Autosomal dominant nonsyndromic deafness 58

  6425. USPi007-A (DFNA58-ipsc-dup2-cl5)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Autosomal dominant nonsyndromic deafness 58

  6426. UTHSCHi001-A (NDC-AD01)

    United States The University of Texas Health Science Center at Houston (UTHSCH)
    Disease:

    Alzheimer's disease

  6427. UTSWi001-A (FA1)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6428. UTSWi001-A-1 (FA1ic)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6429. UTSWi002-A (FA2)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6430. UTSWi002-A-1 (FA2ic)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6431. UTSWi003-A (FA3)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6432. UTSWi003-A-1 (FA3ic)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  6433. UTUi001-A (TUR1)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  6434. UTUi001-B (TUR2)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  6435. UTUi001-C (TUR3)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  6436. UTUi002-A (TUR-STAB1-B1)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  6437. UTUi003-A (TUR-B1)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  6438. VANYHHi001-A (AF13_VANYHH)

    United States VA New York Harbor Healthcare System (VANYHH)
    Disease:

    Brugada syndrome

  6439. VAPACLi001-A

    United States Veterans Affairs Palo Alto Health Care System: Chen Lab (VAPACL)
    Disease:

    Coronary artery vasospasm

  6440. VAPACLi002-A

    United States Veterans Affairs Palo Alto Health Care System: Chen Lab (VAPACL)
    Disease:

    Coronary artery vasospasm

  6441. VAPACLi003-A

    United States Veterans Affairs Palo Alto Health Care System: Chen Lab (VAPACL)
    Disease:

    Coronary artery vasospasm

  6442. VCCRIi002-A (069)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Spontaneous coronary artery dissection

    Disease:

    Fibromuscular dysplasia

  6443. VCCRIi003-A (SCAD-96 and 096)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Spontaneous coronary artery dissection

    Disease:

    Celiac disease

  6444. VCCRIi018-A (136 and SCAD-136)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Spontaneous coronary artery dissection

  6445. VCCRIi024-A (326)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Normal (average)

  6446. VHIRi001-A (C1(RP25)_UiPSC_mR5F_7)

    Spain Vall d'Hebron Institut de Recerca (VHIR)
    Disease:

    Normal (average)

  6447. VHIRi002-A (C2(RP25)_UiPSC_mR5F_1)

    Spain Vall d'Hebron Institut de Recerca (VHIR)
    Disease:

    Normal (average)

  6448. VHIRi003-A (RP25_UiPSC_mR5F_8)

    Spain Vall d'Hebron Institut de Recerca (VHIR)
    Disease:

    Normal (average)

  6449. VRFi001-A (VRF-RBiPSC01)

    India VISION RESEARCH FOUNDATION (VRF)
    Disease:

    Retinoblastoma

  6450. VRISGi002-A

    Vietnam Vinmec Research Insitute of Stem Cell and Gene Technology (VRISG)
    Disease:

    Normal (average)

  6451. VRISGi004-A (ERY02-hiPSC-CL)

    Vietnam Vinmec Research Insitute of Stem Cell and Gene Technology (VRISG)
    Disease:

    Normal (average)

  6452. VUi001-A (SCZ 14.3 and hvs479)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6453. VUi002-A (SCZ 18.10 and hvs483)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6454. VUi003-A (SCZ 13.2 and hvs478)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6455. VUi004-A (SCZ 19.2 and hvs-484)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6456. VUi005-A (787.3)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6457. VUi006-A (SCZ 21.5)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6458. VUi007-A (786.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6459. VUi008-A (SCZ 6.2)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6460. VUi009-A (SCZ 10.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6461. VUi010-A (SCZ 1.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6462. VUi011-A (SCZ 3.5)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6463. VUi012-A (SCZ 7.2)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6464. VUi013-A (804.3)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6465. VUi014-A (SCZ 11.8 and hvs476)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6466. VUi015-A (SCZ 12.1 and hvs-477)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6467. VUi016-A (789.A1 and hvs341)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6468. VUi017-A (SCZ4.3)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6469. VUi018-A (SCZ 5.1 and hvs487)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6470. VUi019-A (SCZ 15.2 and hvs480)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6471. VUi020-A (SCZ 20.1 and hvs485)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6472. VUi021-A (793.3 and hvs473)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6473. VUi023-A (801.A1 and hvs474)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6474. VUi024-A (SCZ 9.4)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6475. VUi025-A (hvs93)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6476. VUi026-A (hvs97)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6477. VUi027-A (hvs201)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6478. VUi028-A (hvs369)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6479. VUi029-A (hvs449a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6480. VUi030-A (hvs450a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  6481. VUi031-A (hvs88)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6482. VUi032-A (GM23973 Coriell and hvs451a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6483. VUi033-A (hvs445a and GM02036 Coriell)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6484. VUi034-A (hvs-304 and SCZ 8.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6485. VUi035-A (hvs-471 and SCZ 802.2A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6486. VUi036-A (hvs420 and GM23964)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6487. VUi038-A (hvs444a and GM01651 Coriell)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6488. VUi039-A (hvs446a and GM05381 Coriell)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6489. VUi040-B (GB3f)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6490. VUi041-A (GB4d)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6491. VUi041-B (GB4b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6492. VUi042-A (GB2a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6493. VUi047-A (785.10 and hvs337)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6494. VUi048-A (788.A1 and hvs469)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6495. VUi049-A (790.3 and hvs470)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6496. VUi052-A (17.6 and hvs482)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6497. VUi053-A (2.5 and hvs317)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6498. VUi058-A (hvs521a and PEX1-024)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Zellweger spectrum disorders

  6499. VUi059-A (hsv522a and PEX1-025)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Zellweger spectrum disorders

  6500. VUi060-A (hsv523a and PEX1-026)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Zellweger spectrum disorders

  6501. VUi062-A (hvs512b and 7485267)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6502. VUi062-B (hvs512c and 7485267)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6503. VUi062-C (hvs512d and 7485267)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6504. VUi063-A (6300896 and hvs513a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6505. VUi063-B (hvs513b and 6300896)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6506. VUi063-C (hvs513c and 6300896)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6507. VUi064-A (1484443 and hvs514a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6508. VUi064-B (1484443 and hvs514b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6509. VUi064-C (hvs514c and 1484443)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  6510. VUi067-A (785162, hvs462a and 328.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6511. VUi068-A (747417, 238.A and hvs463a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6512. VUi069-A (747412, hvs464b and 237.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6513. VUi069-B (747412, 237.A and hvs464a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6514. VUi070-A (773097, hvs465b and 298.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6515. VUi070-B (773097, hvs465a and 298.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6516. VUi071-A (776649, hvs466b and 307.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6517. VUi071-B (776649, hvs466a and 307.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6518. VUi072-A (hvs467a, 773099 and 297.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6519. VUi073-A (hvs468a, 712461 and 157.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6520. VUi074-A (689209, hvs497a and 113.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6521. VUi074-B (689209, hvs497b and 113.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6522. VUi074-C (689209, 113.C and hvs497c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6523. VUi075-A (105.A, hvs498a and 685694)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6524. VUi075-B (105.B, hvs498b and 685694)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6525. VUi075-C (105.C, hvs498c and 685694)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6526. VUi076-A (1005528, 509.A and hvs499a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6527. VUi076-B (1005528, hvs499b and 509.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6528. VUi076-C (1005528, 509.C and hvs499c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6529. VUi077-A (hvs500a, 781085 and 315.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6530. VUi077-B (hvs500b, 781085 and 315.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6531. VUi077-C (hvs500c, 315.C and 781085)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6532. VUi078-A (hvs501a, 710274 and 152.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6533. VUi078-B (hvs501b, 152.B and 710274)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6534. VUi078-C (hvs501c, 152.C and 710274)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6535. VUi079-A (894067, 470.A and hvs502a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6536. VUi079-B (hvs502b, 894067 and 470.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6537. VUi079-C (hvs502c, 894067 and 470.C)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6538. VUi080-A (293.A, 770533 and hvs503a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6539. VUi080-B (293.B, 770533 and hvs503b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6540. VUi080-C (hvs503c, 293.C and 770533)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6541. VUi081-A (379.A, 837936 and hvs504a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6542. VUi081-B (379.B, 837936 and hvs504b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6543. VUi081-C (379.C, 837936 and hvs504c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6544. VUi082-A (778144, 311.A and hvs505a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6545. VUi082-B (778144, 311.B and hvs505b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6546. VUi082-C (778144, 311.C and hvs505c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6547. VUi083-A (800835, hvs506a and 339.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6548. VUi083-B (800835, 339.B and hvs506b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6549. VUi083-C (800835, 339.C and hvs506c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6550. VUi084-A (674780, hvs507a and 78.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6551. VUi084-B (674780, hvs507b and 78.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6552. VUi084-C (674780, hvs507c and 78.C)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6553. VUi085-A (717583, hvs508a and 175.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6554. VUi085-B (717583, hvs508b and 175.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6555. VUi085-C (717583, 175.C and hvs508c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6556. VUi086-A (738705, hvs509a and 217.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6557. VUi086-B (738705, hvs509b and 217.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6558. VUi086-C (738705, 217.C and hvs509c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6559. VUi087-A (hvs510a, 776639 and 305.A)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6560. VUi087-B (hvs510b, 305.B and 776639)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6561. VUi087-C (hvs510c, 305.C and 776639)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  6562. VUi088-A (hvs515a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6563. VUi088-B (hvs515b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6564. VUi088-C (hvs515c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Barth syndrome

  6565. VUi089-A (hvs-481 and 16.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6566. VUi090-A (hvs533a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6567. VUi090-B (hvs533b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6568. VUi090-C (hvs533c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6569. VUi093-A (hvs472 and 771.1)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  6570. VUi095-A (71066723 and hvs538c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Usp7

  6571. VUi095-B (hvs538b and 71066723)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Usp7

  6572. VUi095-C (71066723 and hvs538a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Usp7

  6573. VUi096-A (hvs542a and 1224409)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Trip12

  6574. VUi096-B (hvs542b and 1224409)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Trip12

  6575. VUi096-C (hvs542c and 1224409)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Trip12

  6576. VUi097-A (hvs557c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Usp7

  6577. VUi097-B (hvs557b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Usp7

  6578. VUi097-C (hvs557a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Usp7

  6579. VUi101-A (hvs575a and 2393801)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6580. VUi101-B (hvs575b and 2393801)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6581. VUi101-C (hvs575c and 2393801)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Microvillus inclusion disease

  6582. VUi103-A (hvs543a and MDN 8482277)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6583. VUi103-B (hvs543b and MDN 8482277)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6584. VUi103-C (MDN 8482277 and hvs543c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Retinitis pigmentosa

  6585. CIGLi001-A-2

    Lithuania Vilnius University (VULSC)
    Disease:

    Normal (average)

  6586. CIGLi001-A-6 (VULSCi002-A-6)

    Lithuania Vilnius University (VULSC)
    Disease:

    Normal (average)

  6587. VUMCi001-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6588. VUMCi002-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6589. VUMCi003-A (1167)

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6590. VUMCi004-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6591. VUMCi005-A (3360)

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6592. VUMCi006-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  6593. VUMCCVi001-A (NS15C5)

    United States Vanderbilt University Medical Center: Cardiovascular Medicine (VUMCCV)
    Disease:

    Normal (average)

  6594. VUMCCVi002-A (NS9C4)

    United States Vanderbilt University Medical Center: Cardiovascular Medicine (VUMCCV)
    Disease:

    Aortic valve stenosis

    Disease:

    Dyslipidemia

    Disease:

    Hypertension

  6595. VUMCCVi003-A (NS18C1)

    United States Vanderbilt University Medical Center: Cardiovascular Medicine (VUMCCV)
    Disease:

    Normal (average)

  6596. VUMCCVi004-A (NS8C1)

    United States Vanderbilt University Medical Center: Cardiovascular Medicine (VUMCCV)
    Disease:

    Coronary artery disease

    Disease:

    Hyperlipidemia

    Disease:

    Atrial fibrillation

  6597. WAi001-A (DF19-9-11T and iPS DF19-9-11T.H)

    United States WiCell Research Institute (WA)
    Disease:

    Normal (average)

  6598. WAi001-B (DF19-9-7T and iPS-DF19-9-7T)

    United States WiCell Research Institute (WA)
    Disease:

    Normal (average)

  6599. WCHi001-A

    China West China Hospital (WCH)
    Disease:

    Normal (average)

  6600. WCHi002-A

    China West China Hospital (WCH)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  6601. WCHi003-A

    China West China Hospital (WCH)
    Disease:

    Schizophrenia

  6602. WCHi004-A

    China West China Hospital (WCH)
    Disease:

    Normal (average)

  6603. WCHi005-A

    China West China Hospital (WCH)
    Disease:

    Bipolar disorder

  6604. WCHi006-A

    China West China Hospital (WCH)
    Disease:

    Schizophrenia

  6605. WCHPSYi001-A

    China Psychiatry Laboratory, West China Hospital, Sichuan University (WCHPSY)
    Disease:

    Schizophrenia

  6606. WCHPSYi002-A

    China Psychiatry Laboratory, West China Hospital, Sichuan University (WCHPSY)
    Disease:

    Schizophrenia

  6607. WIMRi001-A (PKU_LCL_11195)

    Australia Westmead Institute for Medical Research (WIMR)
    Disease:

    Phenylketonuria

  6608. WIMRi002-A (PKU_LCL_01565)

    Australia Westmead Institute for Medical Research (WIMR)
    Disease:

    Phenylketonuria

  6609. WIMRi003-A (PKU_FIB_00937)

    Australia Westmead Institute for Medical Research (WIMR)
    Disease:

    Phenylketonuria

  6610. WIMRi004-A (PKU_FIB_02406)

    Australia Westmead Institute for Medical Research (WIMR)
    Disease:

    Phenylketonuria

  6611. WISi005-A (BF1)

    Israel Weizmann Institute of Science (WIS)
    Disease:

    Normal (average)

  6612. WISi006-A (FX1 iPSC)

    Israel Weizmann Institute of Science (WIS)
    Disease:

    Fragile x syndrome

  6613. WISCi003-A (IPS(FORESKIN)-1)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6614. WISCi004-A (IPS(IMR90)-1)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6615. WISCi004-B (IPS(IMR90)-4 and WAi004-B)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6616. WISCi005-A (DS1 and UWWC1-DS1)

    United States University of Wisconsin (WISC)
    Disease:

    Trisomy 21

  6617. WISCi005-B (DS4 and UWWC1-DS4)

    United States University of Wisconsin (WISC)
    Disease:

    Trisomy 21

  6618. WISCi005-C (UWWC1-DS2U and DS2U)

    United States University of Wisconsin (WISC)
    Disease:

    Trisomy 21

  6619. WISCi006-A (2DS3 and UWWC1-2DS3)

    United States University of Wisconsin (WISC)
    Disease:

    Down syndrome

  6620. WISCi007-A (WC026i-5807-3)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6621. WISCi007-B (WC027i-5807-5)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6622. WISCi007-C (WC028i-5807-6)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6623. WISCi008-A (WC029i-5907-1)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6624. WISCi008-B (WC030i-5907-2)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6625. WISCi008-C (WC031i-5907-6)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6626. WISCi009-A (WC032i-6007-1)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6627. WISCi009-B (WC033i-6007-2)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  6628. WTSIi001-A (HPSI1213i-pahc_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6629. WTSIi001-B (HPSI1213i-pahc_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6630. WTSIi002-A (HPSI0913i-eika_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6631. WTSIi003-A (HPSI1213i-hehd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6632. WTSIi003-B (HPSI1213i-hehd_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6633. WTSIi004-A (HPSI1113i-qolg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6634. WTSIi004-B (HPSI1113i-qolg_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6635. WTSIi005-A (HPSI1113i-podx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6636. WTSIi005-B (HPSI1113i-podx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6637. WTSIi006-A (HPSI1113i-hayt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6638. WTSIi006-B (HPSI1113i-hayt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6639. WTSIi007-A (HPSI1113i-dons_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6640. WTSIi008-A (HPSI1013i-kuxp_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6641. WTSIi009-A (HPSI0913i-diku_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6642. WTSIi010-A (HPSI0314i-xugn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6643. WTSIi010-B (HPSI0314i-xugn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6644. WTSIi011-A (HPSI0314i-qonc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6645. WTSIi011-B (HPSI0314i-qonc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6646. WTSIi012-A (HPSI0314i-bubh_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6647. WTSIi012-B (HPSI0314i-bubh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6648. WTSIi013-A (HPSI0214i-kucg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6649. WTSIi014-A (HPSI0214i-heja_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6650. WTSIi014-B (HPSI0214i-heja_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6651. WTSIi015-A (HPSI0114i-rozh_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6652. WTSIi015-B (HPSI0114i-rozh_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6653. WTSIi016-A (HPSI0114i-oevr_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6654. WTSIi017-A (HPSI0114i-lexy_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6655. WTSIi017-B (HPSI0114i-lexy_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6656. WTSIi018-A (HPSI0114i-kolf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6657. WTSIi018-B (HPSI0114i-kolf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6658. WTSIi018-B-1 (HPSI0114i-kolf_2-C1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6659. WTSIi019-A (HPSI0114i-iisa_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6660. WTSIi019-B (HPSI0114i-iisa_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6661. WTSIi020-A (HPSI0114i-eipl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6662. WTSIi020-B (HPSI0114i-eipl_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6663. WTSIi021-A (HPSI1013i-wuye_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6664. WTSIi021-B (HPSI1013i-wuye_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6665. WTSIi022-A (HPSI1013i-yemz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6666. WTSIi022-B (HPSI1013i-yemz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6667. WTSIi023-A (HPSI0114i-zapk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6668. WTSIi023-B (HPSI0114i-zapk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6669. WTSIi024-A (HPSI0114i-vabj_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6670. WTSIi025-A (HPSI1013i-pamv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6671. WTSIi025-B (HPSI1013i-pamv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6672. WTSIi026-A (HPSI0314i-hoik_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6673. WTSIi027-A (HPSI0913i-oapg_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6674. WTSIi028-A (HPSI1213i-babk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6675. WTSIi029-A (HPSI1013i-garx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6676. WTSIi030-A (HPSI0214i-pelm_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6677. WTSIi030-B (HPSI0214i-pelm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6678. WTSIi031-A (HPSI0314i-bipt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6679. WTSIi032-A (HPSI1113i-bima_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6680. WTSIi032-B (HPSI1113i-bima_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6681. WTSIi033-A (HPSI1013i-aetc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6682. WTSIi034-A (HPSI0913i-kojv_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6683. WTSIi035-A (HPSI0913i-gooj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6684. WTSIi036-A (HPSI1113i-waus_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6685. WTSIi037-A (HPSI0114i-zoxy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6686. WTSIi038-A (HPSI1113i-ieki_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6687. WTSIi038-B (HPSI1113i-ieki_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6688. WTSIi039-A (HPSI1013i-wopl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6689. WTSIi040-A (HPSI0314i-qaqx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6690. WTSIi041-A (HPSI0114i-bezi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6691. WTSIi041-B (HPSI0114i-bezi_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6692. WTSIi042-A (HPSI1013i-jufd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6693. WTSIi042-B (HPSI1013i-jufd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6694. WTSIi044-A (HPSI0214i-eiwy_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6695. WTSIi045-A (HPSI0214i-heth_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6696. WTSIi046-A (HPSI0214i-wibj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6697. WTSIi046-B (HPSI0214i-wibj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6698. WTSIi047-A (HPSI0814i-bokz_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6699. WTSIi047-B (HPSI0814i-bokz_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6700. WTSIi048-A (HPSI0214i-datg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6701. WTSIi049-A (HPSI0514i-wiii_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6702. WTSIi049-B (HPSI0514i-wiii_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6703. WTSIi050-A (HPSI1014i-toss_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6704. WTSIi051-A (HPSI1113i-uofv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6705. WTSIi052-A (HPSI1114i-ziyn_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6706. WTSIi053-A (HPSI0413i-corn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6707. WTSIi054-A (HPSI0413i-nudd_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6708. WTSIi054-B (HPSI0413i-nudd_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6709. WTSIi055-A (HPSI0513i-debk_9)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6710. WTSIi055-B (HPSI0513i-debk_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6711. WTSIi056-A (HPSI0513i-dipe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6712. WTSIi057-A (HPSI0513i-giuf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6713. WTSIi057-B (HPSI0513i-giuf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6714. WTSIi058-A (HPSI0513i-suzg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6715. WTSIi059-A (HPSI0513i-uilw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6716. WTSIi060-A (HPSI0513i-veqz_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6717. WTSIi061-A (HPSI0513i-veve_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6718. WTSIi062-A (HPSI0513i-zaui_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6719. WTSIi063-A (HPSI0613i-aevs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6720. WTSIi064-A (HPSI0613i-bohf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6721. WTSIi065-A (HPSI0613i-eojr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6722. WTSIi065-B (HPSI0613i-eojr_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6723. WTSIi066-A (HPSI0613i-febc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6724. WTSIi066-B (HPSI0613i-febc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6725. WTSIi067-A (HPSI0713i-foop_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6726. WTSIi067-B (HPSI0713i-foop_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6727. WTSIi068-A (HPSI0613i-giuo_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6728. WTSIi068-B (HPSI0613i-giuo_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6729. WTSIi069-A (HPSI0613i-hegp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6730. WTSIi070-A (HPSI0713i-terl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6731. WTSIi070-B (HPSI0713i-terl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6732. WTSIi071-A (HPSI0913i-lise_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6733. WTSIi071-B (HPSI0913i-lise_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6734. WTSIi072-A (HPSI0114i-fikt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6735. WTSIi073-A (HPSI0314i-sojd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6736. WTSIi073-B (HPSI0314i-sojd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6737. WTSIi074-A (HPSI0114i-joxm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6738. WTSIi075-A (HPSI0114i-vass_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6739. WTSIi076-A (HPSI0214i-kehc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6740. WTSIi077-A (HPSI0314i-cuhk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6741. WTSIi077-B (HPSI0314i-cuhk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6742. WTSIi078-A (HPSI0314i-fafq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6743. WTSIi079-A (HPSI1013i-hiaf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6744. WTSIi079-B (HPSI1013i-hiaf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6745. WTSIi080-A (HPSI1013i-sebz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6746. WTSIi081-A (HPSI1113i-qorq_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6747. WTSIi081-B (HPSI1113i-qorq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6748. WTSIi082-A (HPSI1013i-cups_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6749. WTSIi083-A (HPSI1213i-xuja_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6750. WTSIi084-A (HPSI0713i-cicb_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6751. WTSIi084-B (HPSI0713i-cicb_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6752. WTSIi085-A (HPSI1113i-eofe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6753. WTSIi086-A (HPSI0913i-coyi_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6754. WTSIi087-A (HPSI0813i-uaqe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6755. WTSIi088-A (HPSI0913i-ruql_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6756. WTSIi089-A (HPSI0613i-xavk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6757. WTSIi089-B (HPSI0613i-xavk_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6758. WTSIi090-A (HPSI0813i-robp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6759. WTSIi091-A (HPSI0813i-ffdc_11)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6760. WTSIi091-B (HPSI0813i-ffdc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6761. WTSIi092-A (HPSI0713i-nemb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6762. WTSIi093-A (HPSI0413i-sukz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6763. WTSIi094-A (HPSI0613i-xucm_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6764. WTSIi095-A (HPSI0813i-vajx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6765. WTSIi096-A (HPSI0813i-guss_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6766. WTSIi097-A (HPSI0813i-aizi_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6767. WTSIi097-B (HPSI0813i-aizi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6768. WTSIi098-A (HPSI1213i-nekd_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6769. WTSIi099-A (HPSI0813i-civh_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6770. WTSIi099-B (HPSI0813i-civh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6771. WTSIi100-A (HPSI0813i-zexw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6772. WTSIi101-A (HPSI0513i-fejf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6773. WTSIi102-A (HPSI0413i-iakz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6774. WTSIi102-B (HPSI0413i-iakz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6775. WTSIi103-A (HPSI1213i-nusw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6776. WTSIi104-A (HPSI0513i-coio_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6777. WTSIi104-B (HPSI0513i-coio_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6778. WTSIi105-A (HPSI0313i-airc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6779. WTSIi105-B (HPSI0313i-airc_66)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6780. WTSIi105-D (HPSI0313i-airc_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6781. WTSIi106-A (HPSI0613i-hikj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6782. WTSIi106-B (HPSI0613i-hikj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6783. WTSIi107-A (HPSI0813i-iill_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6784. WTSIi107-B (HPSI0813i-iill_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6785. WTSIi108-A (HPSI0313i-cesj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6786. WTSIi109-A (HPSI0413i-coxy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6787. WTSIi109-B (HPSI0413i-coxy_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6788. WTSIi110-A (HPSI0713i-darw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6789. WTSIi110-B (HPSI0713i-darw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6790. WTSIi111-A (HPSI0513i-euir_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6791. WTSIi111-B (HPSI0513i-euir_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6792. WTSIi112-A (HPSI0613i-funp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6793. WTSIi112-B (HPSI0613i-funp_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6794. WTSIi113-A (HPSI0913i-gedo_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6795. WTSIi113-B (HPSI0913i-gedo_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6796. WTSIi114-A (HPSI0513i-golb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6797. WTSIi115-A (HPSI0513i-iasn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6798. WTSIi116-A (HPSI0813i-iicq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6799. WTSIi116-B (HPSI0813i-iicq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6800. WTSIi117-A (HPSI0613i-liun_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6801. WTSIi117-B (HPSI0613i-liun_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6802. WTSIi118-A (HPSI0813i-meqo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6803. WTSIi118-B (HPSI0813i-meqo_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6804. WTSIi119-A (HPSI0613i-oefg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6805. WTSIi120-A (HPSI0513i-oeoo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6806. WTSIi121-A (HPSI0413i-ougl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6807. WTSIi121-B (HPSI0413i-ougl_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6808. WTSIi122-A (HPSI0413i-peop_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6809. WTSIi122-B (HPSI0413i-peop_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6810. WTSIi123-A (HPSI0713i-qimz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6811. WTSIi123-B (HPSI0713i-qimz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6812. WTSIi124-A (HPSI0713i-ruyv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6813. WTSIi124-B (HPSI0713i-ruyv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6814. WTSIi125-A (HPSI0413i-uahf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6815. WTSIi126-A (HPSI0913i-vopm_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6816. WTSIi127-A (HPSI0413i-xekf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6817. WTSIi128-A (HPSI0413i-yuze_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6818. WTSIi129-A (HPSI0613i-zisa_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6819. WTSIi129-B (HPSI0613i-zisa_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6820. WTSIi130-A (HPSI0713i-aehn_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6821. WTSIi130-B (HPSI0713i-aehn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6822. WTSIi131-A (HPSI0513i-aipt_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6823. WTSIi131-B (HPSI0513i-aipt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6824. WTSIi132-A (HPSI0613i-bawa_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6825. WTSIi133-A (HPSI0713i-dard_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6826. WTSIi133-B (HPSI0713i-dard_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6827. WTSIi134-A (HPSI0513i-dulv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6828. WTSIi134-B (HPSI0513i-dulv_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6829. WTSIi135-A (HPSI0214i-feec_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6830. WTSIi135-B (HPSI0214i-feec_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6831. WTSIi136-A (HPSI0913i-iuqb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6832. WTSIi137-A (HPSI0613i-lizq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6833. WTSIi137-B (HPSI0613i-lizq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6834. WTSIi138-A (HPSI0414i-mita_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6835. WTSIi139-A (HPSI1113i-oaaz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6836. WTSIi139-B (HPSI1113i-oaaz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6837. WTSIi140-A (HPSI0613i-oomz_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6838. WTSIi140-B (HPSI0613i-oomz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6839. WTSIi141-A (HPSI0613i-qanu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6840. WTSIi141-B (HPSI0613i-qanu_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6841. WTSIi142-A (HPSI0613i-qony_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6842. WTSIi142-B (HPSI0613i-qony_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6843. WTSIi143-A (HPSI0214i-rayr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6844. WTSIi144-A (HPSI0114i-wegi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6845. WTSIi145-A (HPSI0813i-wots_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6846. WTSIi146-A (HPSI0613i-xosg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6847. WTSIi147-A (HPSI1013i-mijn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6848. WTSIi148-A (HPSI0114i-veui_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6849. WTSIi149-A (HPSI0913i-laia_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6850. WTSIi150-A (HPSI0414i-jetz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6851. WTSIi151-A (HPSI0414i-fixm_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6852. WTSIi152-A (HPSI0414i-eafb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6853. WTSIi153-A (HPSI0414i-puvg_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6854. WTSIi154-A (HPSI0414i-lavd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6855. WTSIi155-A (HPSI0414i-hutq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6856. WTSIi156-A (HPSI0414i-xugr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6857. WTSIi157-A (HPSI0614i-eavo_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6858. WTSIi158-A (HPSI0914i-fuhz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6859. WTSIi159-A (HPSI0714i-gibe_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6860. WTSIi160-A (HPSI0914i-verf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6861. WTSIi161-A (HPSI0714i-rajk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6862. WTSIi162-A (HPSI0914i-lopq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6863. WTSIi163-A (HPSI1014i-suok_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6864. WTSIi164-A (HPSI0614i-foyj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6865. WTSIi165-A (HPSI0414i-reng_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6866. WTSIi166-A (HPSI0414i-wize_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6867. WTSIi167-A (HPSI1013i-funy_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  6868. WTSIi168-A (HPSI0214i-poih_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6869. WTSIi168-B (HPSI0214i-poih_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6870. WTSIi169-A (HPSI0614i-miaj_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6871. WTSIi169-B (HPSI0614i-miaj_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6872. WTSIi170-A (HPSI1213i-tolg_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6873. WTSIi170-B (HPSI1213i-tolg_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6874. WTSIi171-A (HPSI0914i-zerv_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6875. WTSIi171-B (HPSI0914i-zerv_8)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6876. WTSIi172-A (HPSI0914i-laey_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6877. WTSIi172-B (HPSI0914i-laey_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6878. WTSIi173-A (HPSI0414i-naju_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6879. WTSIi174-A (HPSI0614i-paab_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6880. WTSIi174-B (HPSI0614i-paab_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6881. WTSIi175-A (HPSI1014i-tixi_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6882. WTSIi176-A (HPSI0714i-iudw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6883. WTSIi176-B (HPSI0714i-iudw_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6884. WTSIi177-A (HPSI0414i-xojn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6885. WTSIi178-A (HPSI0215i-fawm_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6886. WTSIi178-B (HPSI0215i-fawm_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6887. WTSIi179-A (HPSI0314i-wigw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6888. WTSIi180-A (HPSI0514i-puie_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6889. WTSIi180-B (HPSI0514i-puie_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6890. WTSIi181-A (HPSI0514i-rutc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6891. WTSIi182-A (HPSI0614i-kegd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6892. WTSIi183-A (HPSI0414i-oaqd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6893. WTSIi183-B (HPSI0414i-oaqd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6894. WTSIi184-A (HPSI1014i-qayj_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6895. WTSIi184-B (HPSI1014i-qayj_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6896. WTSIi185-A (HPSI0414i-seru_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6897. WTSIi185-B (HPSI0414i-seru_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6898. WTSIi186-A (HPSI1014i-babz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6899. WTSIi187-A (HPSI1013i-sita_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6900. WTSIi188-A (HPSI1014i-kefb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6901. WTSIi189-A (HPSI1014i-quls_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6902. WTSIi190-A (HPSI0914i-kajh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6903. WTSIi190-B (HPSI0914i-kajh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6904. WTSIi191-A (HPSI0215i-oilg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6905. WTSIi191-B (HPSI0215i-oilg_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6906. WTSIi192-A (HPSI0414i-biiw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6907. WTSIi193-A (HPSI0414i-cekz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6908. WTSIi194-A (HPSI0614i-dixh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6909. WTSIi195-A (HPSI0414i-eevy_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6910. WTSIi195-B (HPSI0414i-eevy_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6911. WTSIi196-A (HPSI0514i-eoxi_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6912. WTSIi197-A (HPSI0714i-fasu_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6913. WTSIi198-A (HPSI0414i-fuai_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6914. WTSIi199-A (HPSI0614i-guyj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6915. WTSIi200-A (HPSI0414i-kefk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6916. WTSIi201-A (HPSI0614i-koqx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6917. WTSIi202-A (HPSI0714i-oebj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6918. WTSIi203-A (HPSI0714i-oojs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6919. WTSIi204-A (HPSI0414i-oulr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6920. WTSIi204-B (HPSI0414i-oulr_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6921. WTSIi205-A (HPSI0514i-pulk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  6922. WTSIi206-A (HPSI0813i-fpdk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6923. WTSIi207-A (HPSI0813i-ffdr_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6924. WTSIi208-A (HPSI0513i-kesz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6925. WTSIi208-B (HPSI0513i-kesz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6926. WTSIi209-A (HPSI0613i-dium_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6927. WTSIi211-A (HPSI0513i-huls_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6928. WTSIi212-A (HPSI0613i-auim_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6929. WTSIi212-B (HPSI0613i-auim_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6930. WTSIi213-A (HPSI0713i-kaks_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6931. WTSIi213-B (HPSI0713i-kaks_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6932. WTSIi214-A (HPSI0513i-leeh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6933. WTSIi214-B (HPSI0513i-leeh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6934. WTSIi216-A (HPSI0613i-riiv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6935. WTSIi216-B (HPSI0613i-riiv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6936. WTSIi217-A (HPSI0513i-cuau_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6937. WTSIi217-B (HPSI0513i-cuau_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6938. WTSIi218-A (HPSI0914i-euts_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6939. WTSIi219-A (HPSI0613i-jorr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6940. WTSIi222-A (HPSI0613i-vorx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6941. WTSIi222-B (HPSI0613i-vorx_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6942. WTSIi223-A (HPSI0813i-piun_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6943. WTSIi225-A (HPSI0513i-xegx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6944. WTSIi225-B (HPSI0513i-xegx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6945. WTSIi227-A (HPSI1113i-wetu_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6946. WTSIi228-A (HPSI0514i-qihv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6947. WTSIi232-A (HPSI0613i-focm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6948. WTSIi233-A (HPSI0513i-cehw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6949. WTSIi235-A (HPSI0513i-uoxz_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6950. WTSIi235-B (HPSI0513i-uoxz_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6951. WTSIi236-A (HPSI0813i-voas_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6952. WTSIi238-A (HPSI0914i-suop_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6953. WTSIi238-B (HPSI0914i-suop_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6954. WTSIi241-A (HPSI0913i-lofv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6955. WTSIi241-B (HPSI0913i-lofv_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6956. WTSIi243-A (HPSI0414i-ceik_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6957. WTSIi243-B (HPSI0414i-ceik_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6958. WTSIi245-A (HPSI0714i-keui_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6959. WTSIi245-B (HPSI0714i-keui_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6960. WTSIi247-A (HPSI0614i-oicx_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6961. WTSIi247-B (HPSI0614i-oicx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6962. WTSIi248-A (HPSI0213i-koun_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6963. WTSIi248-B (HPSI0213i-koun_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6964. WTSIi249-A (HPSI0614i-uilk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6965. WTSIi249-B (HPSI0614i-uilk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6966. WTSIi250-A (HPSI0115i-melw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6967. WTSIi250-B (HPSI0115i-melw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6968. WTSIi252-A (HPSI0115i-vazt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6969. WTSIi252-B (HPSI0115i-vazt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6970. WTSIi253-A (HPSI0514i-letw_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6971. WTSIi253-B (HPSI0514i-letw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6972. WTSIi254-A (HPSI0914i-jejf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6973. WTSIi254-B (HPSI0914i-jejf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6974. WTSIi255-A (HPSI0115i-aion_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6975. WTSIi255-B (HPSI0115i-aion_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6976. WTSIi256-A (HPSI1014i-tuju_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6977. WTSIi256-B (HPSI1014i-tuju_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6978. WTSIi257-A (HPSI0714i-burb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6979. WTSIi257-B (HPSI0714i-burb_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6980. WTSIi258-A (HPSI0913i-bulb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6981. WTSIi259-A (HPSI0514i-vuna_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6982. WTSIi260-A (HPSI0414i-oikd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6983. WTSIi260-B (HPSI0414i-oikd_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6984. WTSIi261-A (HPSI1113i-wahn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6985. WTSIi261-B (HPSI1113i-wahn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6986. WTSIi262-A (HPSI0514i-sohd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6987. WTSIi262-B (HPSI0514i-sohd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6988. WTSIi263-A (HPSI0614i-lepk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6989. WTSIi263-B (HPSI0614i-lepk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6990. WTSIi265-A (HPSI0714i-pipw_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6991. WTSIi265-B (HPSI0714i-pipw_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6992. WTSIi266-A (HPSI0115i-gifk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6993. WTSIi267-A (HPSI0115i-iiyk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6994. WTSIi267-B (HPSI0115i-iiyk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6995. WTSIi268-A (HPSI0714i-nufh_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6996. WTSIi268-B (HPSI0714i-nufh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6997. WTSIi269-A (HPSI0115i-hecn_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6998. WTSIi269-B (HPSI0115i-hecn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  6999. WTSIi270-A (HPSI0514i-fiaj_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7000. WTSIi270-B (HPSI0514i-fiaj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7001. WTSIi271-A (HPSI0414i-gesg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7002. WTSIi274-A (HPSI0714i-jilk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7003. WTSIi274-B (HPSI0714i-jilk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7004. WTSIi275-A (HPSI0115i-uolo_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7005. WTSIi276-A (HPSI1014i-juuy_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7006. WTSIi277-A (HPSI1114i-ualf_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7007. WTSIi277-B (HPSI1114i-ualf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7008. WTSIi279-A (HPSI0813i-ffdj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7009. WTSIi281-A (HPSI0115i-qoog_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7010. WTSIi281-B (HPSI0115i-qoog_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7011. WTSIi283-A (HPSI0514i-toco_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7012. WTSIi284-A (HPSI0614i-liqa_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7013. WTSIi284-B (HPSI0614i-liqa_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7014. WTSIi285-A (HPSI0414i-sebn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7015. WTSIi285-B (HPSI0414i-sebn_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7016. WTSIi287-A (HPSI0514i-lako_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7017. WTSIi287-B (HPSI0514i-lako_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7018. WTSIi288-A (HPSI0715i-meue_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7019. WTSIi288-B (HPSI0715i-meue_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7020. WTSIi291-A (HPSI0215i-yoch_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7021. WTSIi293-A (HPSI0215i-deyz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7022. WTSIi293-B (HPSI0215i-deyz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7023. WTSIi294-A (HPSI1014i-bilx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7024. WTSIi294-B (HPSI1014i-bilx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7025. WTSIi296-A (HPSI0214i-giju_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7026. WTSIi296-B (HPSI0214i-giju_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7027. WTSIi297-A (HPSI0813i-fpdl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7028. WTSIi297-B (HPSI1213i-foqj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7029. WTSIi297-C (HPSI0913i-ffdl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7030. WTSIi297-D (HPSI0813i-fpdl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7031. WTSIi299-A (HPSI0213i-nawk_55)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7032. WTSIi300-A (HPSI0714i-kute_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7033. WTSIi300-B (HPSI0714i-kute_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7034. WTSIi302-A (HPSI1014i-nosn_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7035. WTSIi302-B (HPSI1014i-nosn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7036. WTSIi303-A (HPSI0914i-qehq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7037. WTSIi303-B (HPSI0914i-qehq_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7038. WTSIi308-A (HPSI0115i-zihe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7039. WTSIi310-A (HPSI0614i-ciwj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7040. WTSIi310-B (HPSI0614i-ciwj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7041. WTSIi311-A (HPSI0215i-hipn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7042. WTSIi311-B (HPSI0215i-hipn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7043. WTSIi316-A (HPSI0514i-kuco_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7044. WTSIi316-B (HPSI0514i-kuco_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7045. WTSIi317-A (HPSI1014i-eesb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7046. WTSIi318-A (HPSI1014i-sehl_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7047. WTSIi322-A (HPSI0514i-naah_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7048. WTSIi322-B (HPSI0514i-naah_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7049. WTSIi327-A (HPSI0715i-zaie_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7050. WTSIi327-B (HPSI0715i-zaie_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7051. WTSIi341-A (HPSI1014i-riun_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7052. WTSIi342-A (HPSI0613i-ueah_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7053. WTSIi342-B (HPSI0613i-ueah_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7054. WTSIi345-A (HPSI0715i-aowh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7055. WTSIi347-A (HPSI0814i-doao_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7056. WTSIi347-B (HPSI0814i-doao_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7057. WTSIi349-A (HPSI0914i-gine_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7058. WTSIi350-A (HPSI0513i-momt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7059. WTSIi351-A (HPSI0513i-oibg_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7060. WTSIi353-A (HPSI0914i-ouvb_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7061. WTSIi354-A (HPSI0513i-netf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7062. WTSIi355-A (HPSI0413i-yotv_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7063. WTSIi355-B (HPSI0413i-yotv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7064. WTSIi357-A (HPSI0713i-wiol_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7065. WTSIi362-A (HPSI0513i-oarz_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7066. WTSIi362-B (HPSI0513i-oarz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7067. WTSIi363-A (HPSI1014i-vils_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7068. WTSIi364-A (HPSI1013i-zagm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7069. WTSIi365-A (HPSI0514i-yelp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7070. WTSIi368-A (HPSI0914i-iezw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7071. WTSIi369-A (HPSI0514i-uenn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7072. WTSIi370-A (HPSI0613i-nukw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7073. WTSIi373-A (HPSI1013i-jogf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7074. WTSIi374-A (HPSI1014i-roug_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7075. WTSIi376-A (HPSI0713i-uimo_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7076. WTSIi377-A (HPSI0713i-veku_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7077. WTSIi378-A (HPSI0713i-nocf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7078. WTSIi380-A (HPSI0713i-pusf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7079. WTSIi382-A (HPSI0614i-denw_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7080. WTSIi385-A (HPSI0713i-fett_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7081. WTSIi387-A (HPSI0513i-dovq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7082. WTSIi388-A (HPSI0115i-paim_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7083. WTSIi388-B (HPSI0115i-paim_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7084. WTSIi389-A (HPSI0614i-voce_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7085. WTSIi389-B (HPSI0614i-voce_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7086. WTSIi390-A (HPSI1113i-hajc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7087. WTSIi392-A (HPSI0513i-sucd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7088. WTSIi394-A (HPSI0914i-vaka_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7089. WTSIi396-A (HPSI0414i-kodf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7090. WTSIi398-A (HPSI0414i-rauj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7091. WTSIi399-A (HPSI0614i-gawh_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7092. WTSIi399-B (HPSI0614i-gawh_12)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7093. WTSIi400-A (HPSI0414i-tout_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7094. WTSIi401-A (HPSI0714i-meet_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7095. WTSIi402-A (HPSI0714i-ouzk_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7096. WTSIi402-B (HPSI0714i-ouzk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7097. WTSIi403-A (HPSI0913i-rufg_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7098. WTSIi403-B (HPSI0913i-rufg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7099. WTSIi405-A (HPSI0614i-fovu_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7100. WTSIi405-B (HPSI0614i-fovu_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7101. WTSIi406-A (HPSI0614i-mesr_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7102. WTSIi407-A (HPSI0914i-hidy_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7103. WTSIi407-B (HPSI0914i-hidy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7104. WTSIi408-A (HPSI0414i-niim_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7105. WTSIi408-B (HPSI0414i-niim_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7106. WTSIi409-A (HPSI0414i-walu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7107. WTSIi410-A (HPSI0614i-zoio_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7108. WTSIi410-B (HPSI0614i-zoio_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7109. WTSIi411-A (HPSI0914i-rejf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7110. WTSIi412-A (HPSI0614i-wihj_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7111. WTSIi412-B (HPSI0614i-wihj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7112. WTSIi414-A (HPSI0614i-eisk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7113. WTSIi414-B (HPSI0614i-eisk_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7114. WTSIi415-A (HPSI0614i-laig_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7115. WTSIi415-B (HPSI0614i-laig_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7116. WTSIi416-A (HPSI0514i-aomr_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7117. WTSIi416-B (HPSI0514i-aomr_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7118. WTSIi417-A (HPSI0614i-voxu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7119. WTSIi417-B (HPSI0614i-voxu_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7120. WTSIi419-A (HPSI0514i-kidt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7121. WTSIi420-A (HPSI0914i-tifo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7122. WTSIi420-B (HPSI0914i-tifo_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7123. WTSIi422-A (HPSI0414i-zazi_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7124. WTSIi422-B (HPSI0414i-zazi_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7125. WTSIi424-A (HPSI0514i-mure_9)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7126. WTSIi424-B (HPSI0514i-mure_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7127. WTSIi426-A (HPSI0714i-mejk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7128. WTSIi428-A (HPSI0714i-lutt_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7129. WTSIi430-A (HPSI0514i-aecv_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7130. WTSIi430-B (HPSI0514i-aecv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7131. WTSIi431-A (HPSI0514i-tavh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7132. WTSIi436-A (HPSI0714i-zaos_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7133. WTSIi438-A (HPSI0714i-pirs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7134. WTSIi439-A (HPSI0714i-mitg_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7135. WTSIi444-A (HPSI0714i-riya_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7136. WTSIi445-A (HPSI0714i-xebt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7137. WTSIi446-A (HPSI1113i-vuud_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7138. WTSIi447-A (HPSI0416i-zige_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7139. WTSIi447-B (HPSI0416i-zige_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7140. WTSIi448-A (HPSI0316i-muwv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7141. WTSIi448-B (HPSI0316i-muwv_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7142. WTSIi450-A (HPSI0216i-aiid_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7143. WTSIi450-B (HPSI0216i-aiid_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7144. WTSIi452-A (HPSI0115i-xaka_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7145. WTSIi452-B (HPSI0115i-xaka_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7146. WTSIi453-A (HPSI0416i-fiwt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7147. WTSIi454-A (HPSI0516i-iool_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7148. WTSIi454-B (HPSI0516i-iool_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7149. WTSIi455-A (HPSI0516i-eosr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7150. WTSIi456-A (HPSI0616i-kulz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7151. WTSIi456-B (HPSI0616i-kulz_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7152. WTSIi457-A (HPSI0115i-iinu_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7153. WTSIi457-B (HPSI0115i-iinu_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7154. WTSIi458-A (HPSI0614i-lipl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7155. WTSIi458-B (HPSI0614i-lipl_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7156. WTSIi459-A (HPSI0516i-zukb_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7157. WTSIi459-B (HPSI0516i-zukb_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7158. WTSIi460-A (HPSI0516i-jepf_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7159. WTSIi460-B (HPSI0516i-jepf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7160. WTSIi461-A (HPSI0316i-eoko_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7161. WTSIi461-B (HPSI0316i-eoko_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7162. WTSIi462-A (HPSI0316i-miov_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7163. WTSIi463-A (HPSI0716i-yibs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7164. WTSIi463-B (HPSI0716i-yibs_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7165. WTSIi464-A (HPSI0516i-eitu_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7166. WTSIi464-B (HPSI0516i-eitu_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7167. WTSIi465-A (HPSI0714i-xiry_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7168. WTSIi465-B (HPSI0714i-xiry_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7169. WTSIi466-A (HPSI0416i-aicq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7170. WTSIi466-B (HPSI0416i-aicq_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7171. WTSIi467-A (HPSI0513i-bicb_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7172. WTSIi468-A (HPSI1013i-woci_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7173. WTSIi469-A (HPSI0316i-ierp_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7174. WTSIi470-A (HPSI0516i-jory_9)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7175. WTSIi470-B (HPSI0516i-jory_10)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7176. WTSIi472-A (HPSI0216i-vieg_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7177. WTSIi472-B (HPSI0216i-vieg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7178. WTSIi473-A (HPSI0813i-mioj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7179. WTSIi473-B (HPSI0813i-mioj_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7180. WTSIi474-A (HPSI0216i-dewh_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7181. WTSIi474-B (HPSI0216i-dewh_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7182. WTSIi475-A (HPSI0514i-qajt_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7183. WTSIi475-B (HPSI0514i-qajt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7184. WTSIi476-A (HPSI0813i-peoj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7185. WTSIi477-A (HPSI0514i-kooz_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7186. WTSIi478-A (HPSI0414i-nolz_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7187. WTSIi479-A (HPSI0616i-beyk_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7188. WTSIi479-B (HPSI0616i-beyk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7189. WTSIi480-A (HPSI0516i-iuoc_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7190. WTSIi480-B (HPSI0516i-iuoc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7191. WTSIi481-A (HPSI0716i-toba_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7192. WTSIi482-A (HPSI0616i-gayk_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7193. WTSIi482-B (HPSI0616i-gayk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7194. WTSIi483-A (HPSI0416i-ourj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7195. WTSIi483-B (HPSI0416i-ourj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7196. WTSIi484-A (HPSI0716i-bakv_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7197. WTSIi484-B (HPSI0716i-bakv_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7198. WTSIi485-A (HPSI0614i-kecw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7199. WTSIi485-B (HPSI0614i-kecw_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7200. WTSIi486-A (HPSI0516i-hapz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7201. WTSIi486-B (HPSI0516i-hapz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7202. WTSIi487-A (HPSI0516i-goek_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7203. WTSIi488-A (HPSI0516i-oazw_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7204. WTSIi488-B (HPSI0516i-oazw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7205. WTSIi493-A (HPSI0416i-ruah_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7206. WTSIi493-B (HPSI0416i-ruah_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7207. WTSIi495-A (HPSI0314i-kujn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7208. WTSIi495-B (HPSI0314i-kujn_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7209. WTSIi496-A (HPSI0516i-yibc_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7210. WTSIi497-A (HPSI0616i-oajt_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7211. WTSIi497-B (HPSI0616i-oajt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7212. WTSIi498-A (HPSI0616i-biln_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7213. WTSIi498-B (HPSI0616i-biln_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7214. WTSIi499-A (HPSI0416i-xutl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7215. WTSIi501-A (HPSI0316i-circ_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7216. WTSIi501-B (HPSI0316i-circ_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7217. WTSIi502-A (HPSI0216i-boho_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7218. WTSIi503-A (HPSI0416i-mapx_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7219. WTSIi503-B (HPSI0416i-mapx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7220. WTSIi506-A (HPSI0616i-giql_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7221. WTSIi506-B (HPSI0616i-giql_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7222. WTSIi507-A (HPSI0614i-uevq_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7223. WTSIi507-B (HPSI0614i-uevq_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7224. WTSIi508-A (HPSI0416i-jewl_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7225. WTSIi508-B (HPSI0416i-jewl_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7226. WTSIi509-A (HPSI0416i-ourj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7227. WTSIi510-A (HPSI0216i-xanu_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7228. WTSIi510-B (HPSI0216i-xanu_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7229. WTSIi512-A (HPSI0416i-ruah_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7230. WTSIi514-A (HPSI0416i-iooi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7231. WTSIi514-B (HPSI0416i-iooi_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7232. WTSIi515-A (HPSI0416i-bife_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7233. WTSIi516-A (HPSI0216i-iogu_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7234. WTSIi516-B (HPSI0216i-iogu_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7235. WTSIi518-A (HPSI0416i-cihd_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7236. WTSIi519-A (HPSI0416i-sevr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7237. WTSIi519-B (HPSI0416i-sevr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7238. WTSIi522-A (HPSI0516i-pews_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7239. WTSIi522-B (HPSI0516i-pews_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7240. WTSIi524-A (HPSI0616i-xuvy_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7241. WTSIi525-A (HPSI0616i-bury_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7242. WTSIi525-B (HPSI0616i-bury_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7243. WTSIi526-A (HPSI0316i-qeti_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7244. WTSIi526-B (HPSI0316i-qeti_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7245. WTSIi527-A (HPSI0216i-heub_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7246. WTSIi527-B (HPSI0216i-heub_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7247. WTSIi529-A (HPSI0716i-yipp_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7248. WTSIi529-B (HPSI0716i-yipp_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7249. WTSIi530-A (HPSI0215i-zett_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7250. WTSIi531-A (HPSI0616i-kayf_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7251. WTSIi531-B (HPSI0616i-kayf_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7252. WTSIi534-A (HPSI0616i-eomr_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7253. WTSIi545-A (HPSI0416i-eapo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7254. WTSIi548-A (HPSI0416i-mefc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7255. WTSIi548-B (HPSI0416i-mefc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7256. WTSIi554-A (HPSI0216i-dacv_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7257. WTSIi555-A (HPSI0316i-xaqm_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Congenital hyperinsulinism

  7258. WTSIi558-A (HPSI0516i-oadp_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7259. WTSIi558-B (HPSI0516i-oadp_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7260. WTSIi560-A (HPSI0214i-bute_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7261. WTSIi561-A (HPSI0813i-aomg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7262. WTSIi563-A (HPSI0516i-zujs_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7263. WTSIi564-A (HPSI0313i-fecs_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7264. WTSIi565-A (HPSI0313i-xovo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7265. WTSIi567-A (HPSI0813i-eiqh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7266. WTSIi568-A (HPSI0216i-rihx_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7267. WTSIi569-A (HPSI0613i-qonr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7268. WTSIi569-B (HPSI0613i-qonr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7269. WTSIi570-A (HPSI0213i-koun_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7270. WTSIi571-A (HPSI0513i-pedc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7271. WTSIi573-A (HPSI0115i-qaqp_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7272. WTSIi573-B (HPSI0115i-qaqp_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  7273. WTSIi576-A (HPSI0216i-feht_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7274. WTSIi580-A (HPSI0316i-aask_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  7275. WTSIi582-A (HPSI0613i-oesx_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7276. WTSIi590-A (HPSI0115i-gost_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7277. WTSIi591-A (HPSI0514i-oupf_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7278. WTSIi591-B (HPSI0514i-oupf_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7279. WTSIi593-A (HPSI0514i-tert_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7280. WTSIi593-B (HPSI0514i-tert_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7281. WTSIi594-A (HPSI0115i-aoxv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7282. WTSIi594-B (HPSI0115i-aoxv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7283. WTSIi595-A (HPSI0814i-siqu_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7284. WTSIi595-B (HPSI0814i-siqu_11)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7285. WTSIi596-A (HPSI0514i-oekw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7286. WTSIi597-A (HPSI0414i-uawq_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7287. WTSIi598-A (HPSI1114i-kuul_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7288. WTSIi598-B (HPSI1114i-kuul_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7289. WTSIi599-A (HPSI0614i-lirf_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7290. WTSIi599-B (HPSI0614i-lirf_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7291. WTSIi602-A (HPSI0614i-puhk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7292. WTSIi602-B (HPSI0614i-puhk_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7293. WTSIi603-A (HPSI0614i-qunz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7294. WTSIi603-B (HPSI0614i-qunz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7295. WTSIi607-A (HPSI1014i-xiyh_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7296. WTSIi607-B (HPSI1014i-xiyh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7297. WTSIi609-A (HPSI0516i-suqd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7298. WTSIi609-B (HPSI0516i-suqd_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7299. WTSIi610-A (HPSI1116i-naum_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7300. WTSIi611-A (HPSI0816i-neow_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7301. WTSIi611-B (HPSI0816i-neow_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7302. WTSIi612-A (HPSI0616i-mifg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7303. WTSIi612-B (HPSI0616i-mifg_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7304. WTSIi613-A (HPSI1116i-rafd_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7305. WTSIi613-B (HPSI1116i-rafd_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7306. WTSIi614-A (HPSI0616i-rily_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7307. WTSIi614-B (HPSI0616i-rily_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7308. WTSIi615-A (HPSI0115i-rakq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7309. WTSIi615-B (HPSI0115i-rakq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7310. WTSIi617-A (HPSI0215i-uiao_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7311. WTSIi617-B (HPSI0215i-uiao_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7312. WTSIi618-A (HPSI1114i-xiby_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7313. WTSIi618-B (HPSI1114i-xiby_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7314. WTSIi619-A (HPSI0115i-kozf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7315. WTSIi619-B (HPSI0115i-kozf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7316. WTSIi620-A (HPSI0616i-uegn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7317. WTSIi620-B (HPSI0616i-uegn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7318. WTSIi621-A (HPSI0916i-vorn_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7319. WTSIi621-B (HPSI0916i-vorn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7320. WTSIi622-A (HPSI0516i-menz_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7321. WTSIi622-B (HPSI0516i-menz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7322. WTSIi623-A (HPSI0516i-yist_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7323. WTSIi623-B (HPSI0516i-yist_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7324. WTSIi624-A (HPSI0616i-uofs_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7325. WTSIi624-B (HPSI0616i-uofs_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7326. WTSIi626-A (HPSI0914i-yuvg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7327. WTSIi627-A (HPSI0414i-voqc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7328. WTSIi632-A (HPSI0316i-vats_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7329. WTSIi632-B (HPSI0316i-vats_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7330. WTSIi633-A (HPSI0714i-oatm_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7331. WTSIi633-B (HPSI0714i-oatm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7332. WTSIi634-A (HPSI0115i-timk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7333. WTSIi635-A (HPSI0414i-zabk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Monogenic diabetes

  7334. WTSIi636-A (HPSI0514i-yewo_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7335. WTSIi638-A (HPSI0916i-zipi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7336. WTSIi638-B (HPSI0916i-zipi_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7337. WTSIi641-A (HPSI0516i-aaun_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7338. WTSIi641-B (HPSI0516i-aaun_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7339. WTSIi643-A (HPSI0514i-suul_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7340. WTSIi643-B (HPSI0514i-suul_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7341. WTSIi644-A (HPSI0115i-sehp_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7342. WTSIi644-B (HPSI0115i-sehp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7343. WTSIi645-A (HPSI0514i-xufp_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7344. WTSIi646-A (HPSI1114i-zuuy_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7345. WTSIi646-B (HPSI1114i-zuuy_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7346. WTSIi648-A (HPSI0616i-mesv_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7347. WTSIi648-B (HPSI0616i-mesv_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7348. WTSIi654-A (HPSI0115i-uupc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7349. WTSIi657-A (HPSI0916i-moyn_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7350. WTSIi657-B (HPSI0916i-moyn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7351. WTSIi658-A (HPSI0816i-fuuy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7352. WTSIi659-A (HPSI1116i-wakr_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7353. WTSIi659-B (HPSI1116i-wakr_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7354. WTSIi660-A (HPSI0115i-tiku_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7355. WTSIi660-B (HPSI0115i-tiku_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7356. WTSIi661-A (HPSI0614i-xubw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7357. WTSIi661-B (HPSI0614i-xubw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7358. WTSIi662-A (HPSI1116i-mebq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7359. WTSIi662-B (HPSI1116i-mebq_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7360. WTSIi665-A (HPSI0616i-euia_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7361. WTSIi666-A (HPSI0514i-xayd_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7362. WTSIi666-B (HPSI0514i-xayd_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7363. WTSIi669-A (HPSI0816i-aorf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7364. WTSIi669-B (HPSI0816i-aorf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  7365. WTSIi670-A (HPSI0614i-juzt_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7366. WTSIi672-A (HPSI0516i-quqp_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7367. WTSIi672-B (HPSI0516i-quqp_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7368. WTSIi673-A (HPSI0616i-vaqx_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7369. WTSIi673-B (HPSI0616i-vaqx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7370. WTSIi674-A (HPSI1116i-vozo_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7371. WTSIi674-B (HPSI1116i-vozo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  7372. WTSIi675-A (HPSI0616i-iuse_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7373. WTSIi675-B (HPSI0616i-iuse_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7374. WTSIi676-A (HPSI0616i-heba_11)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7375. WTSIi676-B (HPSI0616i-heba_9)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7376. WTSIi679-A (HPSI0316i-ponl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7377. WTSIi679-B (HPSI0316i-ponl_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7378. WTSIi680-A (HPSI0516i-peoo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7379. WTSIi680-B (HPSI0516i-peoo_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7380. WTSIi685-A (HPSI0416i-ioys_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7381. WTSIi685-B (HPSI0416i-ioys_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7382. WTSIi686-A (HPSI0616i-baxr_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7383. WTSIi686-B (HPSI0616i-baxr_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7384. WTSIi687-A (HPSI0916i-vajy_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7385. WTSIi687-B (HPSI0916i-vajy_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  7386. WTSIi688-A (HPSI1116i-wiau_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7387. WTSIi688-B (HPSI1116i-wiau_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7388. WTSIi689-A (HPSI0616i-newl_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  7389. WTSIi690-A (HPSI0115i-jotn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7390. WTSIi690-B (HPSI0115i-jotn_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7391. WTSIi691-A (HPSI1116i-eiyy_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7392. WTSIi693-A (HPSI1116i-zies_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7393. WTSIi693-B (HPSI1116i-zies_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7394. WTSIi694-A (HPSI0816i-oemk_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7395. WTSIi697-A (HPSI0516i-dewa_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7396. WTSIi697-B (HPSI0516i-dewa_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7397. WTSIi698-A (HPSI1116i-aimh_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7398. WTSIi698-B (HPSI1116i-aimh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7399. WTSIi699-A (HPSI0916i-hikt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7400. WTSIi699-B (HPSI0916i-hikt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7401. WTSIi700-A (HPSI0115i-iuad_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7402. WTSIi700-B (HPSI0115i-iuad_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7403. WTSIi703-A (HPSI0816i-hizl_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7404. WTSIi703-B (HPSI0816i-hizl_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  7405. WTSIi705-A (HPSI0314i-xagu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7406. WTSIi709-A (HPSI0516i-kumr_11)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  7407. WTSIi712-A (HPSI1016i-riwg_8)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare genetic neurological disorder

  7408. WTSIi713-A (HPSI0816i-xoga_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7409. WTSIi713-B (HPSI0816i-xoga_12)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  7410. WTSIi715-A (HPSI0115i-payf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7411. WTSIi717-A (HPSI0916i-helh_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7412. WTSIi717-B (HPSI0916i-helh_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7413. WTSIi718-A (HPSI0616i-duve_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7414. WTSIi718-B (HPSI0616i-duve_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Immune system disease

  7415. WTSIi720-A (HPSI0916i-jejm_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  7416. WTSIi722-A (HPSI0115i-jakt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7417. WTSIi726-A (HPSI0115i-boqx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7418. WTSIi727-A (HPSI0115i-bimq_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7419. WTSIi732-A (HPSI0616i-kalo_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  7420. WTSIi740-A (HPSI0215i-romx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  7421. WYUi001-A

    China Wuyi University (WYU)
    Disease:

    Normal (average)

  7422. WYUi002-A

    China Wuyi University (WYU)
    Disease:

    Normal (average)

  7423. WYUi003-A

    China Wuyi University (WYU)
    Disease:

    Normal (average)

  7424. WYUi004-A (WYU-G6)

    China Wuyi University (WYU)
    Disease:

    Normal (average)

  7425. XACHi004-A

    China Xi'an children's hospital (XACH)
    Disease:

    Atrial fibrillation

  7426. XCHIDi001-A (ZZY250101)

    China Xi'an Children's Hospital (XCHID)
    Disease:

    Primary ciliary dyskinesia

  7427. XDCMHi001-A

    China Xiaoshan District Chinese Medicine Hospital (XDCMH)
    Disease:

    Ankylosing spondylitis

  7428. XJHi001-A

    China Xijing Hospital (XJH)
    Disease:

    Fibronectin glomerulopathy

  7429. XMDYYYi001-A (BDU-iPSCs)

    China Department of Neurology, The First Affiliated Hospital of Xiamen University (XMDYYY)
    Disease:

    Becker muscular dystrophy

  7430. XMUi001-A

    China Xiamen University (XMU)
    Disease:

    Primary coenzyme q10 deficiency 7

  7431. XWHNi001-A

    China Department of Neurology, Xuan Wu Hospital (XWHN)
    Disease:

    Alzheimer's disease

  7432. XWHNi002-A

    China Department of Neurology, Xuan Wu Hospital (XWHN)
    Disease:

    Normal (average)

  7433. XWHNi003-A

    China Department of Neurology, Xuan Wu Hospital (XWHN)
    Disease:

    Alzheimer's disease

  7434. XWHNi004-A

    China Department of Neurology, Xuan Wu Hospital (XWHN)
    Disease:

    Normal (average)

  7435. XXMUFAi001-A

    China The First Affiliated Hospital of Xinxiang Medical University (XXMUFA)
    Disease:

    Long qt syndrome 2

  7436. YBLi001-A (YBL/IPSC01/CONTROL)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7437. YBLi002-A (YBL/IPSC002/CONTROL)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7438. YBLi003-A (YBL/IPSC05/CONTROL)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7439. YBLi004-A (YBL/SH/2018/0062)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7440. YBLi005-A (YBL/OS/2021/00196)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7441. YBLi006-A (YBL/PH/2022/0025)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)

  7442. YBLi007-A (YBL/SH/2018/0067)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7443. YBLi008-A (YBL/SH/2018/0050)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  7444. YCMi003-A

    South Korea College of Medicine (YCM)
    Disease:

    Dilated cardiomyopathy

  7445. YCMi004-A

    South Korea College of Medicine (YCM)
    Disease:

    Dilated cardiomyopathy

  7446. YCMi005-A

    South Korea College of Medicine (YCM)
    Disease:

    Dilated cardiomyopathy

  7447. YCMi006-A

    South Korea College of Medicine (YCM)
    Disease:

    Hypertrophic cardiomyopathy

  7448. YCMi007-A

    South Korea College of Medicine (YCM)
    Disease:

    Dilated cardiomyopathy

  7449. YCMi009-A (YCMi009-hDCM009-A)

    South Korea College of Medicine (YCM)
    Disease:

    Dilated cardiomyopathy

  7450. YCMi010-A

    South Korea College of Medicine (YCM)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  7451. YSCHi001-A (2AMJH)

    South Korea Severance Children’s Hospital (YSCH)
    Disease:

    Epilepsy

  7452. YSCHi002-A (2ABWS)

    South Korea Severance Children’s Hospital (YSCH)
    Disease:

    Epilepsy

  7453. YUi002-A (VK0846 #1 and ASmut1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7454. YUi003-A (PB9282 #1 and ASmut2)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7455. YUi004-A (PZ8594 #2 and ASmut3)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7456. YUi005-A (ASmut4 and WD1374 #1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7457. YUi006-A (YO1058 #5 and ASdel1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7458. YUi007-A (SD6010 #3 and ASdel2)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7459. YUi008-A (VE1371 #2 and ASdel3)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7460. YUi009-A (DY5863 #21 and ASupd1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7461. YUi010-A (AK7856 #1 and ASupd2)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7462. YUi011-A (ZM9576 #9 and ASupd3)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7463. YUi012-A (QC7748 #2 and ASupd4)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7464. YUi013-A (UI5640 #8 and ASicd1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7465. YUi014-A (DX6976 #7 and ASicd2)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7466. YUi015-A (SL9656 #4 and ASicd3)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  7467. YUi016-A (VJ9612 #5 and ASctr1)

    United States Yale University (YU)
    Disease:

    Normal (average)

  7468. YUi017-A (BT2657 #12 and ASctr2)

    United States Yale University (YU)
    Disease:

    Normal (average)

  7469. YUi018-A (SF6987 #1 and ASctr3)

    United States Yale University (YU)
    Disease:

    Normal (average)

  7470. YUCMi020-A

    South Korea Yonsei University College of Medicine (YUCM)
    Disease:

    Normal (average)

  7471. YUCMi022-A (hiPSC-KCNH2_G53S)

    South Korea Yonsei University College of Medicine (YUCM)
    Disease:

    Long qt syndrome

  7472. YUCMi024-A (hiPSC-KCNQ1_G245G_2)

    South Korea Yonsei University College of Medicine (YUCM)
    Disease:

    Long qt syndrome

  7473. YUCMi025-A (hiPSC-KCNQ1_G245G_1)

    South Korea Yonsei University College of Medicine (YUCM)
    Disease:

    Long qt syndrome

  7474. ZIPi013-B (ZIP13 clone 2)

    Germany Zentrum für Integrative Psychiatrie-ZiP gGmbH, Stem Cell Lab (ZIP)
    Disease:

    Normal (average)

  7475. 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

  7476. ZJUi009-A (ZJULLi001-A)

    China Zhejiang University (ZJU)
    Disease:

    Marfan syndrome

  7477. ZJUi010-A (ZJULLi002-A and 161103SPYLQTFSDC12)

    China Zhejiang University (ZJU)
    Disease:

    Long qt syndrome

  7478. ZJUi011-A (ZJULLi003-A and LSYMYH7iPS)

    China Zhejiang University (ZJU)
    Disease:

    Hypertrophic cardiomyopathy

  7479. ZJUi012-A (ZJULLi004-A and ZYLMYBPC3iPS)

    China Zhejiang University (ZJU)
    Disease:

    Hypertrophic cardiomyopathy

  7480. ZJUCHi003-A

    China The Children's Hospital, Zhejiang University School of Medicine (ZJUCH)
    Disease:

    Temple-baraitser syndrome

  7481. ZJULLi002-A (ZJULLi005-A and JMLMYH6iPSC)

    China Zhejiang University Lianglab (ZJULL)
    Disease:

    Hypertrophic cardiomyopathy 14

  7482. ZJULLi006-A

    China Zhejiang University Lianglab (ZJULL)
    Disease:

    Brugada syndrome

  7483. ZJULLi007-A

    China Zhejiang University Lianglab (ZJULL)
    Disease:

    Normal (average)

  7484. ZJULLi009-A (YYY-iPSC)

    China Zhejiang University Lianglab (ZJULL)
    Disease:

    Wilson disease

  7485. ZJULLi010-A

    China Zhejiang University Lianglab (ZJULL)
    Disease:

    Fabry disease

  7486. ZOCi001-A

    China Zhongshan Ophthalmic Center (ZOC)
    Disease:

    Retinitis pigmentosa

  7487. ZSPHARi002-A

    China Department of Pharmacy (ZSPHAR)
    Disease:

    Kidney disorder

  7488. ZSZOCi001-A

    China Zhongshan Ophthalmic Center (ZSZOC)
    Disease:

    Knobloch syndrome

  7489. ZZUi004-A (ZZU-iPS-SCA3-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 3

  7490. ZZUi005-A (ZZU-iPS-PD-RAB39b-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_parkinson's disease

  7491. ZZUi006-A (ZZU-iPS-DM1-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Steinert myotonic dystrophy

  7492. ZZUi007-A (ZZU-iPS-PD-CHCHD2-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_parkinson's disease

  7493. ZZUi009-A (ZZU-iPS-AD-PS1-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_alzheimer's disease

  7494. ZZUi010-A (ZZU-iPS-AD-APP-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_alzheimer's disease

  7495. ZZUi011-A (ZZU-iPS-Normal-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7496. ZZUi012-A (ZZU-iPS-PFBC-SLC20A2-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Bilateral striopallidodentate calcinosis

  7497. ZZUi013-A (ZZU-iPS-AD-MEOX2-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_alzheimer's disease

  7498. ZZUi014-A (ZZU-iPS-SCA3-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 3

  7499. ZZUi015-A (ZZU-iPS-DM1-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Myotonic dystrophy type 1

  7500. ZZUi016-A

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7501. ZZUi017-A (ZZU-iPS-SCA6-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 6

  7502. ZZUi018-A (ZZU-iPS-SCA6-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7503. ZZUi019-A (ZZU-iPS-Normal-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7504. ZZUi024-A (ZZU-iPS-AD-APP-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Alzheimer's disease

  7505. ZZUi026-A (ZZU-iPS-SCA3-003)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 3

  7506. ZZUi027-A (ZZU-iPS-PD-RAB39b-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Parkinson disease

  7507. ZZUi028-A (ZZU-iPS-Normal-005)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7508. ZZUi030-A (ZZU-iPS-SPG7-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Spastic paraplegia type 7

  7509. ZZUi031-A (ZZU-iPS-Normal-006)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7510. ZZUi036-A (ZZU-iPS-NIID-NOTCH2NLC-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  7511. ZZUi037-A (ZZU-iPS-SCA3-004)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 3

  7512. ZZUCSBi001-A

    China Shu-Ang Li (ZZUCSB)
    Disease:

    Normal (average)

  7513. ZZUNEUi001-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Normal (average)

  7514. ZZUNEUi002-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Spinocerebellar ataxia type 3

  7515. ZZUNEUi003-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Wilson disease

  7516. ZZUNEUi004-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Wilson disease

  7517. ZZUNEUi005-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Wilson disease

  7518. ZZUNEUi010-A (CMF001-A)

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Juvenile amyotrophic lateral sclerosis

  7519. ZZUNEUi026-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Hypertrophic cardiomyopathy

  7520. ZZUNEUi027-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Long qt syndrome 2

  7521. ZZUNEUi028-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Hypertrophic cardiomyopathy

  7522. ZZUNEUi029-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Hypercholesterolemia

  7523. ZZUNEUi030-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Long qt syndrome

  7524. ZZUSAHi004-A

    China The Second Affiliated Hospital of Zhengzhou University (ZZUSAH)
    Disease:

    Familial long qt syndrome