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. AHJNMUi001-A

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

    Arrhythmogenic right ventricular cardiomyopathy

  9. AHMUi001-A

    China dongmei ji (AHMU)
    Disease:

    Leber hereditary optic neuropathy

  10. AHMUi004-A (AHMUMTi004-1)

    China dongmei ji (AHMU)

  11. AHQUi001-A (IPS35-2)

    China Affiliated Hospital of Qingdao University (AHQU)
    Disease:

    Non rare in europe: hyperlipoproteinemia type 4

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

    China Affiliated Hospital of Qingdao University (AHQU)
    Disease:

    Non rare in europe: hyperlipoproteinemia type 4

  13. AIBNi015-A (SPG1-AU01C15)

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

    Hereditary spastic paraplegia 56

  14. AIBNi016-A (SPG2-S376C1)

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

    Hereditary spastic paraplegia 56

  15. AIBNi017-A (SPGh1-S075mC2)

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

    Hereditary spastic paraplegia 56

  16. AIBNi018-A (SPGh2-S964pC6)

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

    Hereditary spastic paraplegia 56

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

  73. AMUFAHi001-A

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

    Normal (average)

  74. AMUFAHi002-A (AY20210813)

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

    Polycystic ovary syndrome

  75. AMUFAHi003-A

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

    Normal (average)

  76. RUCDRi002-A-72

    Austria Angios GmbH (ANGIOS)
    Disease:

    Normal (average)

  77. AOUMEYi002-A

    Italy Meyer Children's Hospital IRCCS (AOUMEY)

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Normal (average)

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

  81. ASGRCi004-A (0118 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Proliferative diabetic retinopathy

    Disease:

    Type 2 diabetes mellitus

  82. ASGRCi005-A (0622 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Keratoconjunctivitis sicca

  83. ASGRCi006-A (0808 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Proliferative diabetic retinopathy

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

  85. ATCi002-A

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

    Keipert syndrome

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

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

    Hepatocyte nuclear factor 1-alpha-associated monogenic diabetes

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

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

    Hepatocyte nuclear factor 1-alpha-associated monogenic diabetes

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Maturity-onset diabetes of the young type 10

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

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

    Maturity-onset diabetes of the young type 10

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Maturity-onset diabetes of the young type 10

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

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

    Diabetes mellitus

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

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

    Diabetes mellitus

  102. AUi001-A

    Denmark Aarhus University (AU)
    Disease:

    Herpes simplex encephalitis

  103. AUMCi001-A (LUMC0195iFOXC)

    Netherlands Amsterdam University Medical Centers (AUMC)

  104. AUMCi002-A (LUMC0203iOCA)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Oculocutaneous albinism type 1a

  105. AUMCi003-A (LUMC0147iXLRS)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    X-linked retinoschisis

  106. AUMCi004-A (LUMC0181iXLRS)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    X-linked retinoschisis

  107. AUMCi005-A (LUMC0182iXLRS)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    X-linked retinoschisis

  108. AUMCi006-A (LUMC0196iOAT)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Gyrate atrophy of choroid and retina

  109. AUMCi007-A (LUMC0204iOAT)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Gyrate atrophy of choroid and retina

  110. AUMCi008-A (LUMC0296iOAT)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Gyrate atrophy of choroid and retina

  111. AUMCi009-A (LUMC0251iSLC)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

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

  112. BBANTWi001-A (iPSC_FB_M45-50_C9)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  113. BBANTWi001-B (iPSC_FB_M45-50_C15)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  114. BBANTWi001-C (iPSC_FB_M45-50_C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  115. BBANTWi006-A (iPSC_BrS9_FB_C7)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome 1

  116. BBANTWi007-A (iPSC_BrS10_FB_C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome 1

  117. BBANTWi008-A (iPSC_PBMC_LDS_SMAD3_T1_C11)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 3

  118. BBANTWi009-A

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Meester-loeys syndrome

  119. BBANTWi010-A (iPSC_PBMC_LDS_TGFB3_KE2M_C9)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 5

  120. BBANTWi011-A

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Familial thoracic aortic aneurysm and aortic dissection

  121. BBANTWi012-A (F1990.01 C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal (average)

  122. BBANTWi012-A-1 (TTN_E48_V4623*)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

  123. BBANTWi012-A-2 (iPSC_FB_F19901C3_TTN_E48_L4612*)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

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

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

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

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Dilated cardiomyopathy

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

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

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  304. BCHNi001-A (BCHi001-A)

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

    Bardet-biedl syndrome

  305. BCHNCi001-A

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

    Early infantile epileptic encephalopathy

  306. BCHNCi003-A

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

    Mitochondrial pyruvate carrier deficiency

  307. BCHNDi001-A

    China 徐超龙 (BCHND)
    Disease:

    Mitochondrial encephalomyopathy

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

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal (average)

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

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal (average)

  310. BCMi002-A (LZ02)

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal (average)

  311. BCMi003-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked mental retardation syndrome

  312. BCMi004-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked mental retardation syndrome

  313. BCMi005-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked mental retardation syndrome

  314. BCMi006-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked mental retardation syndrome

  315. BCMi007-A

    United States Baylor College of Medicine (BCM)
    Disease:

    Lubs x-linked mental retardation syndrome

  316. BCRTi001-A (P01-1)

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

    Fibrodysplasia ossificans progressiva

  317. BCRTi002-A (P02-1)

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

    Fibrodysplasia ossificans progressiva

  318. BCRTi004-A

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

    Normal (average)

  319. BCRTi005-A

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

    Normal (average)

  320. BCRTi006-A

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

    Focal segmental glomerulosclerosis

  321. BCRTi007-A

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

    Polycystic kidney disease

  322. BCRTi009-A

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

    Diabetic nephropathy

  323. BCRTi010-A

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

    Normal (average)

  324. BCRTi011-A

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

    Neurofibromatosis type 1

  325. BFVSBi001-A

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

    Arterial calcification

  326. BFVSBi003-A

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

    Ehlers-danlos syndrome, vascular type

  327. BFVSBi004-A

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

    Ehlers-danlos syndrome, vascular type

  328. BGUi001-A (BGU01iPORhet)

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

    P450 oxidoreductase deficiency

  329. BGUi002-A (BGU02iPOR)

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

    P450 oxidoreductase deficiency

  330. BGUi003-A (BGU03iPOR)

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

    P450 oxidoreductase deficiency

  331. BGUi004-A (BGU101iCCHS)

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

    Congenital central hypoventilation syndrome

  332. BGUi005-A (BGU102iCCHS)

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

    Congenital central hypoventilation syndrome

  333. BGUi008-A (DCM-C)

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

    Left ventricular noncompaction cardiomyopathy

  334. BGUi009-A (DCM-O)

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

    Left ventricular noncompaction cardiomyopathy

  335. BGUi010-A (DCM-R)

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

    Left ventricular noncompaction cardiomyopathy

  336. BGUi011-A (BGU01iGRIN2D)

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

    Developmental and epileptic encephalopathy, 46

  337. BGUi012-A (BGU02iGRIN2D CTR)

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

  340. BGUi015-A (BGUiBJ)

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

    Normal (average)

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  343. BIHi001-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  344. BIHi001-B-1

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  345. BIHi001-B-7

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  346. BIHi001-B-8

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  347. BIHi002-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Autosomal recessive osteopetrosis 4

  348. BIHi004-A (NHDF Epi5 Cl5 iPSC)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  349. BIHi004-B (NHDF Epi5 Cl2 iPSC)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  350. BIHi005-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  351. BIHi005-A-4

    Germany Berlin Institute of Health (BIH)
    Disease:

    Myocardial infarction

  352. BIHi005-A-5

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_alzheimer's disease

  353. BIHi006-D

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  354. BIHi007-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  355. BIHi008-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  356. BIHi009-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  357. BIHi010-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  358. BIHi011-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  359. BIHi012-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  360. BIHi015-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  361. BIHi016-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  362. BIHi017-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  363. BIHi018-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  364. BIHi019-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  365. BIHi024-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  366. BIHi025-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  367. BIHi028-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  368. BIHi029-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  369. BIHi030-C

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  370. BIHi031-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  371. BIHi032-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  372. BIHi038-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  373. BIHi049-A (SCVI-112)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Donnai-barrow syndrome

  375. BIHi250-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  376. BIHi266-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  377. BIHi267-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

  378. BIHi269-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  379. BIHi276-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

  380. BIOi002-A

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Autosomal dominant optic atrophy

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

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Hereditary retinal dystrophy

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Frontotemporal dementia

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Huntington disease

  389. STBCi006-A-1 (ApoE KO)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  392. BIONi010-A (K1P53)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Inflammatory disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  422. 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)

  423. 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)

  424. 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)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

  429. BIONi010-C-72

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  437. BIONi016-A (H310715 47-1)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  447. BIONi026-A (H300715 48-3)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  454. BIONi033-A (H180615 and SAMEA4563389)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  455. BIONi034-A (H290715 and SAMEA4563391)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  456. BIONi035-A (H180815 and SAMEA4563393)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  459. BIORTCi001-A (BAiPSC 000 and OSTiFGM2)

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

    Normal (average)

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

    Hungary BioTalentum Ltd. (BIOT)
    Disease:

    Obsolete_alzheimer's disease

  461. BIUi001-A (T1A1i-001)

    Israel Bar Ilan University (BIU)
    Disease:

    Obsolete: nuclear cell envelopathy

  462. BIUi002-A (T1A1i-002)

    Israel Bar Ilan University (BIU)
    Disease:

    Obsolete: nuclear cell envelopathy

  463. BJTTHi001-A

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Normal (average)

  464. BJTTHi001-A-1

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  465. BJTTHi001-A-2

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Dravet syndrome

    Disease:

    Epilepsy

  466. BJTTHi001-A-3

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  467. BJTTHi001-A-4

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  468. BJTTHi001-A-5

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  469. BJTTHi003-A (CARASIL WHN1C2)

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Carasil syndrome

  470. BRCi014-A (1383D6 and HPS1006)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Normal (average)

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

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Oligodendrocyte

  472. BRCi021-A (TUH1)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Cardiomyopathy

  473. BRCi024-A (HiPS-RTT_CUH01)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  474. BRCi025-A (HiPS-RTT_CUH02)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  475. BRCi026-A (HiPS-RTT_CUH05)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  476. BRCi027-A (HiPS-RTT_CUH06)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  477. BRCi036-A (HiPS-GLUT1DS1)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Classic glucose transporter type 1 deficiency syndrome

  478. BRCi037-A (HiPS-GLUT1DS2)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Classic glucose transporter type 1 deficiency syndrome

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

    United States Boston University (BUCREM)
    Disease:

    Lethal brain and heart developmental defects

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

    United States Boston University (BUCREM)
    Disease:

    Lethal brain and heart developmental defects

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

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

    Retinitis pigmentosa

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

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

    Age-related macular degeneration

  486. CAMi001-A (KiPS c1)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  487. CAMi002-A (FiPS 2a)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  488. CAMi002-B (FiPS 2b)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  489. CAMi002-C (FiPS 2c)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  490. CAMi004-A (AdiPS 1)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  491. CAMi005-A (O27Tat)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  492. CAMi005-B (2F8)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal (average)

  493. CAMi014-A (A1ATD1)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Alpha-1-antitrypsin deficiency

  494. CBi001-A (XLC-348)

    United States Creative Bioarray (CB)
    Disease:

    Obsolete_schizophrenia

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

    United States Creative Bioarray (CB)
    Disease:

    Obsolete_schizophrenia

  496. CBCHi001-A-1

    China Beijing Chest Hospital (CBCH)
    Disease:

    Hypertrophic cardiomyopathy

  497. CBDTi001-A

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

    Normal (average)

  498. CBIGi001-A (AIW002-02)

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

    Normal (average)

  499. CBIGi001-A-1 (PRKN-KO and PRKN-KO/AIW002-02)

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

    Parkinson disease

  500. CBIGi001-A-2 (PINK1-KO and PINK1-KO/AIW002-02)

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

    Parkinson disease

  501. CBIGi001-A-3 (PINK1-KO/PRKN-KO/AIW002-02 and PINK1-KO/PRKN-KO)

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

    Parkinson disease

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

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

    Parkinson disease

  503. CBIGi002-A-1 (GBA W378G-correction/2890 and 2890-iso)

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

    Parkinson disease

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

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

    Parkinson disease

  505. CBIGi003-A-1 (3026-iso and GBA N370S-correction/3026)

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

    Parkinson disease

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

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

    Normal (average)

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Normal (average)

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

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

    Myotonic dystrophy type 1

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Normal (average)

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

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

    Congenital myotonic dystrophy

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

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

    Dilated cardiomyopathy

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

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

    Dilated cardiomyopathy

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

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

    Normal (average)

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

  527. CCMi001-A (DMD1)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Duchenne muscular dystrophy

  528. CCMi007-A (SAS1 C5)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  529. CCMi008-A (SAS2 C1)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  530. CCMi009-A (SAS3 C10)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  531. CCMi011-A (SAS7 C6)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  532. CCMi012-A (LMNA_SP_C3)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Dilated cardiomyopathy

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

    Austria St. Anna Kinderkrebsforschung GmbH (CCRI)
    Disease:

    Normal (average)

  534. CDIi001-A (01279)

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

    Normal (average)

  535. CDIi002-A (01434)

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

    Normal (average)

  536. CDIi004-A (11713)

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

    Normal (average)

  537. CDIi011-A (21527)

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

    Normal (average)

  538. CDIi013-A (PPMI_3409 and FCDI_11287)

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

    Parkinson disease

  539. CDIi014-A (FCDI_11292 and PPMI_4055)

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

    Parkinson disease

  540. CDIi015-A (PPMI_3419 and FCDI_11294)

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

    Parkinson disease

  541. CDIi016-A (PPMI_3411 and FCDI_11295)

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

    Normal (average)

  542. CDIi017-A (PPMI_3446 and FCDI_11296)

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

    Parkinson disease

  543. CDIi018-A (PPMI_3234 and FCDI_11298)

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

    Parkinson disease

  544. CDIi019-A (PPMI_52062 and FCDI_11299)

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

    Parkinson disease

  545. CDIi019-A-1

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

    Parkinson disease

  546. CDIi019-A-2

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

    Parkinson disease

  547. CDIi020-A (PPMI_54144 and FCDI_11300)

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

    Prodromal period

    Disease:

    Parkinson disease

  548. CDIi021-A (PPMI_3459 and FCDI_11301)

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

    Parkinson disease

  549. CDIi022-A (FCDI_11302 and PPMI_3460)

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

    Normal (average)

  550. CDIi023-A (FCDI_11303 and PPMI_3448)

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

    Parkinson disease

  551. CDIi024-A (FCDI_11305 and PPMI_51867)

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

    Prodromal period

    Disease:

    Parkinson disease

  552. CDIi025-A (FCDI_11306 and PPMI_40273)

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

    Parkinson disease

  553. CDIi026-A (FCDI_11307 and PPMI_51625)

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

    Parkinson disease

  554. CDIi027-A (FCDI_11308 and PPMI_3186)

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

    Parkinson disease

  555. CDIi028-A (PPMI_3664 and FCDI_11309)

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

    Parkinson disease

  556. CDIi029-A (PPMI_3665 and FCDI_11310)

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

    Parkinson disease

  557. CDIi030-A (FCDI_11311 and PPMI_3668)

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

    Normal (average)

  558. CDIi031-A (PPMI_3451 and FCDI_11312)

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

    Parkinson disease

  559. CDIi032-A (FCDI_11313 and PPMI_3658)

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

    Normal (average)

  560. CDIi033-A (FCDI_11314 and PPMI_3465)

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

    Parkinson disease

  561. CDIi034-A (PPMI_51440 and FCDI_11317)

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

    Parkinson disease

  562. CDIi035-A (PPMI_51330 and FCDI_11318)

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

    Prodromal period

    Disease:

    Parkinson disease

  563. CDIi036-A (PPMI_42072 and FCDI_11319)

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

    Prodromal period

    Disease:

    Parkinson disease

  564. CDIi037-A (PPMI_52530 and FCDI_11321)

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

    Parkinson disease

  565. CDIi038-A (FCDI_11323 and PPMI_53339)

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

    Parkinson disease

  566. CDIi039-A (FCDI_11325 and PPMI_56761)

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

    Parkinson disease

  567. CDIi040-A (FCDI_11327 and PPMI_3220)

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

    Parkinson disease

  568. CDIi041-A (FCDI_11328 and PPMI_56435)

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

    Parkinson disease

  569. CDIi042-A (PPMI_41486 and FCDI_11329)

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

    Parkinson disease

  570. CDIi043-A (PPMI_54262 and FCDI_11331)

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

    Prodromal period

    Disease:

    Parkinson disease

  571. CDIi044-A (PPMI_50184 and FCDI_11334)

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

    Prodromal period

    Disease:

    Parkinson disease

  572. CDIi045-A (FCDI_11337 and PPMI_3952)

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

    Normal (average)

  573. CDIi046-A (FCDI_11340 and PPMI_56779)

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

    Prodromal period

    Disease:

    Parkinson disease

  574. CDIi047-A (FCDI_11341 and PPMI_3471)

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

    Parkinson disease

  575. CDIi048-A (PPMI_3453 and FCDI_11342)

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

    Normal (average)

  576. CDIi049-A (PPMI_3480 and FCDI_11343)

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

    Normal (average)

  577. CDIi050-A (PPMI_4098 and FCDI_11344)

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

    Parkinson disease

  578. CDIi050-A-1

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

    Parkinson disease

  579. CDIi050-A-2

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

    Parkinson disease

  580. CDIi051-A (PPMI_3452 and FCDI_11345)

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

    Normal (average)

  581. CDIi052-A (PPMI_4091 and FCDI_11346)

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

    Parkinson disease

  582. CDIi053-A (PPMI_3422 and FCDI_11347)

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

    Parkinson disease

  583. CDIi054-A (FCDI_11348 and PPMI_50086)

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

    Parkinson disease

  584. CDIi055-A (FCDI_11349 and PPMI_60003)

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

    Prodromal period

    Disease:

    Parkinson disease

  585. CDIi056-A (PPMI_51971 and FCDI_11353)

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

    Parkinson disease

  586. CDIi057-A (PPMI_56954 and FCDI_11355)

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

    Prodromal period

    Disease:

    Parkinson disease

  587. CDIi058-A (FCDI_11362 and PPMI_51755)

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

    Prodromal period

    Disease:

    Parkinson disease

  588. CDIi059-A (PPMI_52828 and FCDI_11363)

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

    Prodromal period

    Disease:

    Parkinson disease

  589. CDIi060-A (FCDI_11370 and PPMI_55251)

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

    Parkinson disease

  590. CDIi061-A (FCDI_11371 and PPMI_55380)

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

    Prodromal period

    Disease:

    Parkinson disease

  591. CDIi062-A (FCDI_11436 and PPMI_90456)

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

    Prodromal period

    Disease:

    Parkinson disease

  592. CDIi063-A (FCDI_11437 and PPMI_3473)

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

    Parkinson disease

  593. CDIi064-A (PPMI_3475 and FCDI_11438)

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

    Parkinson disease

  594. CDIi065-A (PPMI_3588 and FCDI_11442)

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

    Parkinson disease

  595. CDIi066-A (FCDI_11446 and PPMI_4111)

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

    Parkinson disease

  596. CDIi067-A (FCDI_11447 and PPMI_3960)

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

    Parkinson disease

  597. CDIi068-A (FCDI_11448 and PPMI_51518)

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

    Parkinson disease

  598. CDIi069-A (PPMI_3666 and FCDI_11449)

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

    Parkinson disease

  599. CDIi070-A (FCDI_11450 and PPMI_3966)

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

    Normal (average)

  600. CDIi071-A (PPMI_4108 and FCDI_11455)

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

    Parkinson disease

  601. CDIi072-A (FCDI_11459 and PPMI_4101)

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

    Parkinson disease

  602. CDIi073-A (PPMI_52400 and FCDI_11460)

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

    Prodromal period

    Disease:

    Parkinson disease

  603. CDIi074-A (PPMI_54908 and FCDI_11462)

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

    Prodromal period

    Disease:

    Parkinson disease

  604. CDIi075-A (PPMI_54991 and FCDI_11463)

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

    Prodromal period

    Disease:

    Parkinson disease

  605. CDIi076-A (PPMI_56680 and FCDI_11465)

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

    Prodromal period

    Disease:

    Parkinson disease

  606. CDIi077-A (PPMI_3469 and FCDI_11468)

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

    Parkinson disease

  607. CDIi078-A (FCDI_11469 and PPMI_3467)

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

    Parkinson disease

  608. CDIi079-A (PPMI_57670 and FCDI_11471)

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

    Prodromal period

    Disease:

    Parkinson disease

  609. CDIi080-A (FCDI_11473 and PPMI_51844)

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

    Parkinson disease

  610. CDIi081-A (PPMI_57447 and FCDI_11474)

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

    Prodromal period

    Disease:

    Parkinson disease

  611. CDIi082-A (PPMI_4099 and FCDI_11475)

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

    Parkinson disease

  612. CDIi083-A (PPMI_52524 and FCDI_11478)

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

    Prodromal period

    Disease:

    Parkinson disease

  613. CDIi084-A (FCDI_11483 and PPMI_57292)

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

    Prodromal period

    Disease:

    Parkinson disease

  614. CDIi085-A (FCDI_11484 and PPMI_3954)

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

    Parkinson disease

  615. CDIi086-A (PPMI_18567 and FCDI_11486)

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

    Prodromal period

    Disease:

    Parkinson disease

  616. CDIi087-A (PPMI_4106 and FCDI_11491)

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

    Parkinson disease

  617. CDIi088-A (PPMI_4107 and FCDI_11492)

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

    Parkinson disease

  618. CDIi089-A (FCDI_11493 and PPMI_4109)

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

    Parkinson disease

  619. CDIi090-A (FCDI_11494 and PPMI_4110)

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

    Parkinson disease

  620. CDIi091-A (FCDI_11498 and PPMI_51714)

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

    Prodromal period

    Disease:

    Parkinson disease

  621. CDIi092-A (FCDI_11500 and PPMI_56169)

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

    Prodromal period

    Disease:

    Parkinson disease

  622. CDIi093-A (PPMI_3953 and FCDI_11505)

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

    Parkinson disease

  623. CDIi094-A (FCDI_11508 and PPMI_52517)

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

    Prodromal period

    Disease:

    Parkinson disease

  624. CDIi095-A (FCDI_11512 and PPMI_53988)

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

    Parkinson disease

  625. CDIi096-A (FCDI_11526 and PPMI_57961)

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

    Prodromal period

    Disease:

    Parkinson disease

  626. CDIi097-A (FCDI_11527 and PPMI_3591)

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

    Parkinson disease

  627. CDIi098-A (FCDI_11545 and PPMI_52932)

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

    Prodromal period

    Disease:

    Parkinson disease

  628. CDIi099-A (FCDI_11546 and PPMI_53518)

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

    Prodromal period

    Disease:

    Parkinson disease

  629. CDIi100-A (FCDI_11555 and PPMI_42378)

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

    Parkinson disease

  630. CDIi101-A (FCDI_11556 and PPMI_40760)

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

    Parkinson disease

  631. CDIi102-A (FCDI_11557 and PPMI_41430)

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

    Parkinson disease

  632. CDIi103-A (FCDI_11571 and PPMI_58182)

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

    Prodromal period

    Disease:

    Parkinson disease

  633. CDIi104-A (FCDI_11578 and PPMI_54048)

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

    Prodromal period

    Disease:

    Parkinson disease

  634. CDIi105-A (PPMI_41568 and FCDI_14555)

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

    Parkinson disease

  635. CEBi001-A (Cellartis Human iPS Cell Line 22)

    France Takara Bio Europe AB (former Cellartis) (CEB)
    Disease:

    Normal (average)

  636. CEGHUi001-A (iPSC_CEGH_C2)

    Brazil Human Genome and Stem Cell Research Center, University of São Paulo (CEGHU)
    Disease:

    Normal (average)

  637. CENSOi001-B (FB78R2c2 and CENSOi249)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  638. CENSOi002-B (FB74R2c4 and CENSOi261)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  639. CENSOi003-B (FB79R2c6 and CENSOi258)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  640. CENSOi005-A (FB76R2c5 and CENSOi245)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  641. CENSOi007-A (FB75R2c5 and CENSOi255)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Duchenne muscular dystrophy

  642. CENSOi008-A (FB77R2c3 and CENSOi260)

    United Kingdom Censo an Axol Bioscience Company (CENSO)
    Disease:

    Myotonic dystrophy type 1

  643. CHCMUi001-A

    China Children's hospital of Chongqing Medical University (CHCMU)
    Disease:

    Activated pi3k-delta syndrome

  644. CHCMUi002-A

    China Children's hospital of Chongqing Medical University (CHCMU)
    Disease:

    Chronic granulomatous disease

  645. CHDIi001-A (#1c8 and CHDI-90002149)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  646. CHDIi002-A (#2c3 and CHDI-90002150)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  647. CHDIi003-A (#3c1 and CHDI-90002151)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  648. CHDIi004-A (#4c2 and CHDI-90002152)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  649. CHDIi005-A (#5c4 and CHDI-90002153)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  650. CHDIi006-A (#6c7 and CHDI-90002154)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  651. CHDIi008-A (#8c3 and CHDI-90002156)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  652. CHDIi010-A (#10c2 and CHDI-90002158)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  653. CHDIi011-A (#11c2 and CHDI-90002159)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  654. CHDIi013-A (#13c5 and CHDI-90002161)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  655. CHDIi014-A (#14c1 and CHDI-90002162)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  656. CHDIi016-A (#16c6 and CHDI-90002164)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  657. CHDIi017-A (#17c1 and CHDI-90002165)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  658. CHDIi018-A (#18c1 and CHDI-90002166)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  659. CHDIi019-A (#19c9 and CHDI-90002167)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  660. CHDIi020-A (#20c2 and CHDI-90002168)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  661. CHDIi021-A (#21c5 and CHDI-90002169)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  662. CHDIi022-A (#22c1 and CHDI-90002170)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  663. CHDIi023-A (#23c8 and CHDI-90002171)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  664. CHDIi024-A (#24c7 and CHDI-90002172)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  665. CHDIi026-A (#26c3 and CHDI-90002174)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  666. CHDIi027-A (#27c4 and CHDI-90002175)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  667. CHDIi028-A (#28c3 and CHDI-90002176)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  668. CHDIi029-A (#29c4 and CHDI-90002177)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  669. CHDIi031-A (#31c1 and CHDI-90002179)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  670. CHDIi033-A (#104c2 and CHDI-90002181)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  671. CHDIi034-A (#105c1 and CHDI-90002182)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  672. CHDIi035-A (#108c5 and CHDI-90002183)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  673. CHDIi036-A (#110c5 and CHDI-90002184)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  674. CHDIi038-A (#112c7 and CHDI-90002186)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  675. CHDIi040-A (#115c6 and CHDI-90002188)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  676. CHDIi041-A (#116c2 and CHDI-90002189)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  677. CHDIi042-A (#117c5 and CHDI-90002190)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  678. CHDIi043-A (#118c6 and CHDI-90002191)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  679. CHDIi044-A (#120c3 and CHDI-90002192)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  680. CHDIi045-A (#121c6 and CHDI-90002193)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  681. CHDIi046-A (#122c1 and CHDI-90002194)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  682. CHDIi047-A (#123c6 and CHDI-90002195)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  683. CHDIi048-A (#125c2 and CHDI-90002196)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  684. CHDIi049-A (#127c2 and CHDI-90002197)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  685. CHDIi050-A (#128c3 and CHDI-90002198)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  686. CHDIi051-A (#129c1 and CHDI-90002199)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  687. CHDIi054-A (#132c3 and CHDI-90002202)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  688. CHDIi055-A (#133c5 and CHDI-90002203)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  689. CHDIi056-A (#134c3 and CHDI-90002204)

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

  690. CHDTRi001-B (HT953B and iSP1.2.2B)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Cln3

  691. CHDTRi002-B (HT954B and iSP5.2.1B)

    United States Division of Translational Research, NICHD, NIH (CHDTR)

  692. CHDTRi003-A (HT955A and iSP5.2.2A)

    United States Division of Translational Research, NICHD, NIH (CHDTR)

  693. CHDTRi004-B (HT956B and iSP8.2.1B)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Cln3

  694. CHDTRi005-A (iSP10.2.1A and HT957A)

    United States Division of Translational Research, NICHD, NIH (CHDTR)
    Disease:

    Cln3

  695. CHDTRi006-E (HT958E and iSP29.2.2E)

    United States Division of Translational Research, NICHD, NIH (CHDTR)

  696. CHOCi005-A

    United States CHOC Children's (CHOC)
    Disease:

    Gm1 gangliosidosis

  697. CHOPi001-A (CHOPJMML1854)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Juvenile myelomonocytic leukemia

  698. CHOPi005-A (LD0638.0A)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Hypomyelination with atrophy of basal ganglia and cerebellum

  699. CHOPi006-A (LD0313.0)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Hypomyelination with atrophy of basal ganglia and cerebellum

  700. CHOPi007-A

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Hypomyelination with atrophy of basal ganglia and cerebellum

  701. CHOPi008-A (TMD145.T21.G1S)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Transient abnormal myelopoiesis associated with down syndrome

  702. CHOPi008-B (TMD145.E46.G1S)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Transient abnormal myelopoiesis associated with down syndrome

  703. CHOPi008-C (DS145.T21.G1)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Transient abnormal myelopoiesis associated with down syndrome

  704. CHOPi012-A (CHOPACTG2-R257C)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Megacystis-microcolon-intestinal hypoperistalsis syndrome 5

  705. CHOPi013-A (CHOPWT17_TPM1KOc28)

    United States The Children's Hospital of Philadelphia (CHOP)
    Disease:

    Normal (average)

  706. CHULAi001-A (GPDi001-A)

    Thailand Chulalongkorn University (CHULA)
    Disease:

    Glucose-6-phosphate dehydrogenase deficiency

  707. CHUQi001-A (522-2666-2 and SAMEA104271492)

    Canada CHU de Québec-Université Laval Research Center (CHUQ)
    Disease:

    Myotonic dystrophy type 1

  708. CHUVi001-A

    Switzerland Centre Hospitalier Universitaire Vaudois (CHUV)
    Disease:

    Normal (average)

  709. CHWi001-A

    China The centre of prenatal diagnosis, The Central Hospital of Wenzhou (CHW)
    Disease:

    Intellectual disability

  710. CIAUi002-C (UBC3 M1)

    Australia Centenary Institute of Cancer Medicine and Cell Biology (CIAU)
    Disease:

    Left bundle branch block

    Disease:

    Nonischemic cardiomyopathy

  711. CIAUi003-A (MCCIi005-A-1 and BFC4)

    Australia Centenary Institute of Cancer Medicine and Cell Biology (CIAU)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia 2

  712. 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

  713. 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)

  714. 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)

  715. CIMHi001-A (CIMHi44f028#4)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  716. CIMHi002-A (CIMHi29m067#3)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  717. CIMHi003-A (CIMHi23m035#2)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  718. CIMHi004-A (CIMHi24f007#4)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  719. CIMHi005-A (CIMHi25f100#5)

    Germany Central Institute of Mental Health (CIMH)
    Disease:

    Normal (average)

  720. CIMRi001-A (GM27291)

    United States Coriell Institute for Medical Research (CIMR)
    Disease:

    Vici syndrome

  721. CIPi001-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)
    Disease:

    Benign familial infantile epilepsy

  722. CIPi002-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)

  723. CIPi004-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)

  724. CIPi005-A

    China Children’s Hospital of Capital Institute of Pediatrics (CIP)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  725. CIRAi005-A (F2KU1#4 and F2KU1)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  726. CIRAi005-A-1 (IsC2-F2KU1#4 and IsC-F2KU1)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  727. CIRAi006-A (F2KU2#17 and F2KU2)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  728. CIRAi006-A-1 (IsC-F2KU2 and IsC41-F2KU2#17)

    Japan Center for iPS Cell Research and Application (CIRA)
    Disease:

    Facioscapulohumeral muscular dystrophy 2

  729. CIRMi001-A (CW13000)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  730. CIRMi002-A (CW13002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  731. CIRMi003-A (CW13003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  732. CIRMi004-A (CW13005)