hPSCreg®
This website uses cookies to keep track of login sessions and for internal Matomo Statistics. See our Privacy Policy for details. This website uses cookies, learn more

Search results

Sort by:

Filter by:

  1. AAKIPSi002-A

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

    Aniridia

  2. AAKIPSi003-A

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

    Aniridia

  3. ABi002-A

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

    Cone dystrophy with supernormal rod response

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

  11. AMUFAHi001-A

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

    Normal

  12. AMUFAHi002-A (AY20210813)

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

    Polycystic ovary syndrome

  13. WAe009-A-36 (JPH2-KO)

    China Anzhen Hospital (ANZHEN)
    Disease:

    Hypertrophic cardiomyopathy

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Normal

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

  17. ASGRCi004-A (0118 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Proliferative diabetic retinopathy

    Disease:

    Type 2 diabetes mellitus

  18. ASGRCi006-A (0808 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Proliferative diabetic retinopathy

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

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

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

    Normal

  21. AUi001-A

    Denmark Aarhus University (AU)
    Disease:

    Herpes simplex encephalitis

  22. BBANTWi008-A (iPSC_PBMC_LDS_SMAD3_T1_C11)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 3

  23. BCHNi001-A (BCHi001-A)

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

    Bardet-biedl syndrome

  24. BCMi002-A (LZ02)

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal

  25. BCRTi002-A (P02-1)

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

    Fibrodysplasia ossificans progressiva

  26. BCRTi004-A

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

    Normal

  27. BGUi002-A (BGU02iPOR)

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

    P450 oxidoreductase deficiency

  28. BGUi003-A (BGU03iPOR)

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

    P450 oxidoreductase deficiency

  29. BGUi004-A (BGU101iCCHS)

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

    Congenital central hypoventilation syndrome

  30. BGUi005-A (BGU102iCCHS)

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

    Congenital central hypoventilation syndrome

  31. BGUi008-A (DCM-C)

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

    Left ventricular noncompaction cardiomyopathy

  32. BGUi009-A (DCM-O)

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

    Left ventricular noncompaction cardiomyopathy

  33. BGUi010-A (DCM-R)

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

    Left ventricular noncompaction cardiomyopathy

  34. BGUi011-A (BGU01iGRIN2D)

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

    Developmental and epileptic encephalopathy, 46

  35. BGUi012-A (BGU02iGRIN2D CTR)

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

    Normal

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

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

    Normal

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

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

    Normal

  38. BGUi015-A (BGUiBJ)

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

    Normal

  39. BIHi004-A (NHDF Epi5 Cl5 iPSC)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  40. BIHi005-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  41. BIHi006-D

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  42. BIHi007-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  43. BIHi008-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  44. BIHi009-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  45. BIHi010-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  46. BIHi011-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  47. BIHi012-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  48. BIHi016-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  49. BIHi017-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  50. BIHi018-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  51. BIHi019-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  52. BIHi024-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  53. BIHi025-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  54. BIHi028-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  55. BIHi029-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  56. BIHi030-C

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  57. BIHi031-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  58. BIHi032-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  59. BIHi038-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  60. BIHi250-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  61. BIHi266-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  62. BIHi267-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

  63. BIHi269-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  64. BIHi276-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

  67. BIONi010-A (K1P53)

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

  88. BIONi016-A (H310715 47-1)

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

  103. BIONi033-A (H180615 and SAMEA4563389)

    Denmark Bioneer (BION)
    Disease:

    Normal

  104. BIONi034-A (H290715 and SAMEA4563391)

    Denmark Bioneer (BION)
    Disease:

    Normal

  105. BIONi035-A (H180815 and SAMEA4563393)

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  108. BIUi001-A (T1A1i-001)

    Israel Bar Ilan University (BIU)
    Disease:

    Obsolete: nuclear cell envelopathy

  109. BIUi002-A (T1A1i-002)

    Israel Bar Ilan University (BIU)
    Disease:

    Obsolete: nuclear cell envelopathy

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

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

    Retinitis pigmentosa

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

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

    Age-related macular degeneration

  115. CBi001-A (XLC-348)

    United States Creative Bioarray (CB)
    Disease:

    Obsolete_schizophrenia

  116. CBIGi001-A (AIW002-02)

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

    Normal

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Normal

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

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

    Myotonic dystrophy type 1

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

    Austria Children's Cancer Research Institute St. Anna Kinderkrebsforschung e. V. (CCRI)
    Disease:

    Normal

  124. CDIi001-A (01279)

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

    Normal

  125. CDIi002-A (01434)

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

    Normal

  126. CDIi004-A (11713)

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

    Normal

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

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

    Normal

  128. CEBe012-A (SA121)

    Sweden Takara Bio Europe AB (former Cellartis) (CEB)

  129. CEBe013-A (SA142)

    Sweden Takara Bio Europe AB (former Cellartis) (CEB)

  130. CEBe033-A (SA001)

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

    Normal

  131. CEBe034-A (SA002)

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

    Patau syndrome

  132. CEBe034-A-1 (SA002.5)

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

    Patau syndrome

  133. CENSOi002-B (FB74R2c4 and CENSOi261)

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

    Duchenne muscular dystrophy

  134. CENSOi003-B (FB79R2c6 and CENSOi258)

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

    Duchenne muscular dystrophy

  135. CENSOi005-A (FB76R2c5 and CENSOi245)

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

    Duchenne muscular dystrophy

  136. CENSOi007-A (FB75R2c5 and CENSOi255)

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

    Duchenne muscular dystrophy

  137. CENSOi008-A (FB77R2c3 and CENSOi260)

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

    Myotonic dystrophy type 1

  138. CHAe002-A (CHA-hES4)

    South Korea Pochon CHA University (CHA)

  139. CHAHESe001-A (CHA-hES NT6 and CHA-NTK6)

    South Korea CHA University (CHAHES)
    Disease:

    Age-related macular degeneration

  140. CHCMUi001-A

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

    Activated pi3k-delta syndrome

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

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

    Transient abnormal myelopoiesis associated with down syndrome

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

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

    Transient abnormal myelopoiesis associated with down syndrome

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

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

    Transient abnormal myelopoiesis associated with down syndrome

  187. CHWi001-A

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

    Intellectual disability

  188. CIPi001-A

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

    Benign familial infantile epilepsy

  189. CIPi002-A

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

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

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

    Facioscapulohumeral muscular dystrophy 2

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

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

    Facioscapulohumeral muscular dystrophy 2

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

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

    Facioscapulohumeral muscular dystrophy 2

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

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

    Facioscapulohumeral muscular dystrophy 2

  194. CMCi001-A (CMC-KIN-hiPSC)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Karyomegalic interstitial nephritis

  195. CMCi002-A (CMC-GIT-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Gitelman syndrome

  196. CMCi006-A (CMC-Fb-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

  197. CMCi009-A (CMC-BHD-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Birt-hogg-dube syndrome

  198. CMFTe001-A (Man-2)

    United Kingdom Central Manchester and Manchester Children's University Hospitals NHS (CMFT)

  199. CMGANTi003-A (SEMD1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  200. CMGANTi004-A (SEMD2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  201. CMGANTi005-A (iPSC_MFS_FBN1_MCE-KB_C8)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Marfan syndrome

  202. CMUi002-A

    China Capital Medical University (CMU)
    Disease:

    Normal

  203. CPGHi004-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal

  204. CPGHi006-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Autosomal dominant polycystic kidney disease

  205. CPGHi007-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal

  206. CRICKi001-A (iFCI001)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Intellectual disability

  207. CRICKi002-A (iFCI027)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Intellectual disability

  208. CRICKi007-A (iFCI009)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    Spinal muscular atrophy with lower extremity predominant

  209. CRICKi008-A (iFCI006 and NH13-0078)

    United Kingdom The Francis Crick Institute Limited (CRICK)
    Disease:

    X-linked centronuclear myopathy

  210. CRMi001-A (NCRM-5 and NL-5)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal

  211. CRMi003-A (NCRM-1 and NL-1)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal

  212. CRMi004-A (CR0000007, NCRM-2 and ND50030)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal

  213. CRMi005-A (CR0000011, ND50021 and ND1.4)

    United States National Institutes of Health - Center for Regenerative Medicine (CRM)
    Disease:

    Normal

  214. CRTDi003-A (CRTD2)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  215. CRTDi003-B (CRTD3)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  216. CRTDi004-A (CRTD1)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  217. CRTDi005-A (CRTD4)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  218. CRTDi005-B (CRTD5)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  219. CRTDi006-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  220. CRTDi006-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  221. CRTDi007-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  222. CRTDi007-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  223. CRTDi008-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  224. CRTDi009-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  225. CRTDi010-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  226. CRTDi011-A (IDP52555 #9)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  227. CRTDi011-B (IDP52555 #13)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  228. CRTDi011-C (IDP52555 #36)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  229. CRTDi011-D (IDP52555 #44)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  230. CSSi013-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Normal

  231. CSSi014-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Mucopolysaccharidosis ii

  232. CSSi016-A

    Italy Fondazione Casa Sollievo della Sofferenza IRCCS (CSS)
    Disease:

    Charcot-marie-tooth disease type 4b3

  233. CSUe004-A (chHES-20)

    China Central South University (CSU)

  234. CSUe005-A (chHES-22)

    China Central South University (CSU)

  235. CSUXHi002-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Spinocerebellar ataxia type 1

  236. CSUXHi004-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Waardenburg syndrome type 1

  237. CSUXHEi001-A

    China Central South University (CSUXHE)
    Disease:

    Normal

  238. CSUXHEi002-A

    China Central South University (CSUXHE)
    Disease:

    Normal

  239. CUIMCi004-A (1514_1)

    United States Columbia University Irving Medical Center (CUIMC)
    Disease:

    Class 3 obesity

  240. CVTTHi001-A

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)
    Disease:

    Activated pi3k-delta syndrome

  241. DANi001-C (iPS-CCD-C3)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Normal

  242. DANi002-C (GBA-002-C3)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson's disease

  243. DANi003-H (GBA-003-C8)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson's disease

  244. DANi004-A (PRKN-004-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson's disease

  245. DANi006-F (GBA-006-C6)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson's disease

  246. DANi008-F (SNCA-008-C6)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson's disease

  247. DANi009-C (SNCA-009-C3)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson's disease

  248. DANi010-A (GBA-010-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson's disease

  249. DANi011-A (LRRK2-011-C1)

    Denmark Danish Research Institute of Translational Neuroscience (DAN)
    Disease:

    Parkinson's disease

  250. DHMi001-A (Control_S)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal

  251. DHMi002-A (HLHS_606)

    Germany German Heart Center Munich (DHM)
    Disease:

    Hypoplastic left heart syndrome

  252. DHMi003-A (HLHS_612)

    Germany German Heart Center Munich (DHM)
    Disease:

    Hypoplastic left heart syndrome

  253. DHMi004-A (HOS_1460)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  254. DHMi005-A (Control_L)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal

  255. DHMi005-A-2 (L_FLAG Clone 5)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal

  256. DMBi001-A-2

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Normal

  257. DRICUi003-A (LC56A10005A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimers disease

  258. DRICUi004-A (LC56A10012A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimers disease

  259. DRICUi005-A (LW44A10001A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimers disease

  260. DRICUi006-A (ADANG10496CA)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimers disease

  261. DRICUi007-A (ADANG10605CA)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimers disease

  262. DRICUi009-A (ADLON44426UC)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Normal

  263. DRICUi010-A (BS38A10004A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimers disease

  264. DRICUi011-A (BS38A10002A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimers disease

  265. DRICUi013-A (SC45A10021A)

    United Kingdom UK Dementia Research Institute, Cardiff University (DRICU)
    Disease:

    Late-onset alzheimers disease

  266. WAe009-A-58 (COL4A5 heterozygote)

    China Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine (DZMH)
    Disease:

    Alport syndrome

  267. EDi001-A (AST22, AST23 and SAMEA3319992)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  268. EDi001-A-1 (AST22-C and AST23-C)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  269. EDi001-A-2 (AST23-1KO-3, AST22-1KO-3, AST-23_SCAKO Clone 3 and AST-22_SNCAKO Clone 3)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  270. EDi001-A-3 (AST23_SNCAKO Clone 1, AST22-1KO-1, AST23-1KO-1 and AST22_SNCAKO Clone 1)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  271. EDi001-A-4 (AST22-2KO-6, AST23_SNCAKO Clone 6, AST22_SNCAKO Clone 6 and AST23-2KO-6)

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  272. EDi008-B (G51D-4, EDINi008-B, EDIi008-B and SAMEA3174606)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  273. EDi010-A (RCi136)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  274. EDi010-B (RCi138)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  275. EDi011-A (RCi139)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  276. EDi011-B (RCi140)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  277. EDi011-C (RCi141)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  278. EDi012-A (RCi163)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  279. EDi012-B (RCi164)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  280. EDi012-C (RCi165)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  281. EDi013-A (RCi192)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  282. EDi013-B (RCi193)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  283. EDi013-C (RCi214)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  284. EDi014-A (RCi175)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Unipolar depression

    Disease:

    Anti-social behavior

  285. EDi015-A (RCi176)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Unipolar depression

  286. EDi015-B (RCi183)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Unipolar depression

  287. EDi015-C (RCi184)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Unipolar depression

  288. EDi016-A (RCi189)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  289. EDi016-C (RCi191)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  290. EDi017-A (RCi174)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  291. EDi017-B (RCi181)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  292. EDi017-C (RCi182)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  293. EDi018-A (RCi211)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  294. EDi018-B (RCi212)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  295. EDi018-C (RCi213)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  296. EDi019-A (RCi166)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  297. EDi019-B (RCi167)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  298. EDi019-C (RCi168)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  299. EDi021-A (CS0395iCTR-LBCn3)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  300. EDi022-A (CS0617iCTR-LBCn1)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  301. EDi023-A (CS0791iCTR-LBCn1)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  302. EDi024-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  303. EDi025-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  304. EDi026-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  305. EDi027-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  306. EDi028-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  307. EDi029-A

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  308. EDi031-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  309. EDi032-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  310. EDi033-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  311. EDi034-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  312. EDi035-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  313. EDi036-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  314. EDi037-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  315. EDi038-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  316. EDi040-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  317. EDi041-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  318. EDi042-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  319. EDi043-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  320. EDi044-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  321. EDi045-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  322. EDe006-A (RH 7)

    United Kingdom University of Edinburgh (ED)

  323. EHTJUi002-A (DF-GMP-ZB11AR-H)

    China East Hospital Affiliated to Tongji University (EHTJU)
    Disease:

    Normal

  324. ESi002-A (SP08#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  325. ESi005-A (cFA404-KiPS4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Fanconi anemia

  326. ESi005-B (cFA404-KiPS4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Fanconi anemia

  327. ESi006-A (SP13#4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  328. ESi007-A (CBiPS1sv-4F-40)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  329. ESi028-A (KiPS4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  330. ESi033-A (CBiPS6-2F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  331. ESi038-B (CBiPS32-3F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  332. ESi040-A ([PD] FiPS006-4F-11)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_parkinson's disease

  333. ESi041-A (CBiPS 2F-1c)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  334. ESi041-B (CBiPS 4F-3a)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  335. ESi041-C (CBiPS 4F 10b)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  336. ESi043-A ([ctrl.PD] FiPS005-4F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  337. ESi044-A (FiPS Ctrl1-mR5F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  338. ESi044-B (FiPS Ctrl1-Ep6F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  339. ESi044-C (FiPS Ctrl1-SV4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  340. ESi044-D (FiPS Ctrl1-R4F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  341. ESi045-B (FiPS Ctrl2-Ep6F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  342. ESi046-A ([UCiPS] Ctrl5-R4F-25)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  343. ESi048-A (MS FiPS 1-R4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

  344. ESi049-A (MS FiPS 2 R4F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

  345. ESi050-A (MS FiPS 3-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

  346. ESi051-A (MS FiPS 4-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

  347. ESi052-A (MS FiPS 5-R4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

  348. ESi053-A (MS FiPS 6-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

  349. ESi056-A (AS FiPS 3-Ep6F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Alport syndrome

  350. ESi057-A ([DUP7] FiPS-4F-3-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  351. ESi057-B ([DUPSW] FiPS301-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  352. ESi058-A ([DUP7] FiPS-4F-4-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  353. ESi058-B ([DUP7] FiPS4-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  354. ESi059-A ([SWB] FiPS-4F-1-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  355. ESi059-B ([SWB] FiPS1-R4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  356. ESi060-A ([SWB] FiPS-4F-5-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  357. ESi060-B ([SWB] FiPS5-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  358. ESi065-A ([IDDM1] FiPS 1.13-Ep6F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_type i diabetes mellitus

  359. ESi069-A (SWB FiPS 344-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams-beuren syndrome

  360. ESi070-A (DUPSW FiPS 501-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  361. ESi071-A (DUPSW FiPS 701-R4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  362. ESi072-A (OCD FiPS 1-EP6F-16)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsessive-compulsive disorder

  363. ESi073-A (OCD FiPS 2-EP6F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsessive-compulsive disorder

  364. ESi074-A (CT PBiPS1-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiotoxicity

  365. ESi076-A (BST PBiPS2-Sv4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  366. ESi077-A (CABi001-A and PRPF31-MiPS4F3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Retinitis pigmentosa

  367. ESi078-A (cPRPF31-MiPS4F7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  368. ESi079-A (cAMDdh09-MiPS4F17)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  369. ESi080-A (N1-FiPS4F#7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  370. ESi081-A (SP11#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  371. ESi082-A (CRB1-MiPS4F1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Macular degeneration

  372. ESi085-A (cAMDdh01-MiPS4F8 and DH01 c8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  373. ESi091-A (HLA91-MiPS4F3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  374. ESi092-A (HLA98-MiPS4F15)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  375. ESe009-A (ES-2)

    Spain Spanish Stem Cell Bank (ES)

  376. ESe010-A (ES-3)

    Spain Spanish Stem Cell Bank (ES)

  377. ESe013-A (VAL-5)

    Spain Spanish Stem Cell Bank (ES)

  378. ESe014-A (ES-4 and ES[4])

    Spain Spanish Stem Cell Bank (ES)

  379. ESe015-A (ES-6)

    Spain Spanish Stem Cell Bank (ES)

  380. ESe026-A (ES-11EM)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Hereditary multiple exostoses

  381. ESe028-A (bES[13])

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  382. ESIBIe005-A (HES-5)

    Singapore ES Cell International Pte Ltd. (ESIBI)

  383. WAe009-A-43

    China The First Affiliated Hospital of Guangxi Medical University (FAHGMU)
    Disease:

    Long qt syndrome

  384. WAe001-A-72 (H1-FTO-Knockout-13)

    China The First Affiliated Hospital, School of Medicine (FAHZU)
    Disease:

    Normal

  385. FAMRCi001-A (ARVC2)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  386. FAMRCi001-B (ARVC4)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  387. FAMRCi002-A (OBC7)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Desminopathy

  388. FAMRCi003-A (108-1)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Normal

  389. FAMRCi003-B (108-2)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Normal

  390. FAMRCi004-A (DSPL1)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Sick sinus syndrome

    Disease:

    Atrioventricular block

    Disease:

    Familial progressive cardiac conduction defect

  391. FAMRCi004-B (DSPL10)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Sick sinus syndrome

    Disease:

    Atrioventricular block

    Disease:

    Familial progressive cardiac conduction defect

  392. FAMRCi005-A (LMNA B4)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Paroxysmal ventricular tachycardia

    Disease:

    Atrioventricular block

    Disease:

    Myopathy

  393. FAMRCi005-B (LMNA B5)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Paroxysmal ventricular tachycardia

    Disease:

    Atrioventricular block

    Disease:

    Myopathy

  394. FAMRCi006-A (LMNA T3)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  395. FAMRCi006-B (LMNA T4)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  396. FAMRCi007-A (LMNA #23)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Atrioventricular block

    Disease:

    Paroxysmal atrial fibrillation

  397. FAMRCi007-B (LMNA #19)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Emery-dreifuss muscular dystrophy

    Disease:

    Atrioventricular block

    Disease:

    Paroxysmal atrial fibrillation

  398. FAMRCi008-A (10X-12)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Normal

  399. FAMRCi009-A (RCMP43)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Restrictive cardiomyopathy

  400. FAMRCi010-A (RCMP48)

    Russia Federal Almazov North-West Medical Research Centre (FAMRC)
    Disease:

    Restrictive cardiomyopathy

  401. FDCHDPi001-A (FDCHDP01)

    China Fudan University (FDCHDP)
    Disease:

    Tourette syndrome

  402. FDCHDPe012-A (P4HA2-KO)

    China Fudan University (FDCHDP)
    Disease:

    Normal

  403. FDHPIi001-A

    China (WITHDRAWN) Fudan University (FDHPI)
    Disease:

    Neurodegeneration

  404. FHUSTCi001-A

    China The First Affiliated Hospital of USTC,Division of life Science and Medicine,University of Science and Technology of China (FHUSTC)
    Disease:

    Glomerulopathy

  405. FJMUUHi001-A

    China Fujian Medical University Union Hospital (FJMUUH)
    Disease:

    Parkinson's disease 7

  406. FMCPGHi001-A (301-iPSC-normal-001A)

    China The First Medical Center of PLA General Hospital (FMCPGH)
    Disease:

    Normal

  407. FMCPGHi002-A (301-iPSC-normal-002B)

    China The First Medical Center of PLA General Hospital (FMCPGH)
    Disease:

    Normal

  408. FMUPDCi001-A (ADAT3c.219dupA/c.587C>T)

    China Fetal Medicine unit &Prenatal Diagnosis Center, Shanghai 1st Maternity and Infant Hospital of Tongji University (FMUPDC)
    Disease:

    Mental retardation

  409. FRIMOi001-A (RP1_FiPS4F1.6)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Retinitis pigmentosa

  410. FRIMOi002-A (RP2_FiPS4F2.2)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Retinitis pigmentosa

  411. FRIMOi003-A (STGD1_ FiPS4F1.5)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Stargardt disease

  412. FRIMOi004-A (STGD2_ FiPS4F1.7)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Stargardt disease

  413. FRIMOi005-A (RP3_FiPS4F11)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Retinitis pigmentosa

  414. FRIMOi006-A (BEST1_FiPS4F1)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Bestrophinopathy

  415. FRIMOi007-A (PDE6C_FiPS4F1)

    Spain Fundació de Recerca de l'Institut de Microcirurgia Ocular (FRIMO)
    Disease:

    Achromatopsia

  416. FUHSi001-A

    China Huashan Hospital of Fudan University (FUHS)
    Disease:

    Cervical artery dissection

  417. GENEAe001-A (GENEA001 and SIVF01)

    Australia Genea (GENEA)
    Disease:

    Normal

  418. GENEAe008-A (GENEA009 and SIVF09)

    Australia Genea (GENEA)

  419. GENEAe013-A (GENEA089)

    Australia Genea (GENEA)
    Disease:

    Huntington disease

  420. GENEAe014-A (GENEA029)

    United States Genea (GENEA)
    Disease:

    Normal

  421. GENEAe015-A (GENEA020)

    United States Genea (GENEA)
    Disease:

    Huntington disease

  422. GENEAe016-A (GENEA022)

    Australia Genea (GENEA)
    Disease:

    Normal

  423. GENEAe017-A (GENEA023)

    Australia Genea (GENEA)
    Disease:

    Normal

  424. GENEAe018-A (GENEA090)

    Australia Genea (GENEA)
    Disease:

    Huntington disease

  425. GENEAe019-A (GENEA091)

    Australia Genea (GENEA)
    Disease:

    Huntington disease

  426. GENEAe020-A (GENEA019)

    Australia Genea (GENEA)
    Disease:

    Normal

  427. GENEAe021-A (GENEA021)

    Australia Genea (GENEA)
    Disease:

    Normal

  428. GENYOi001-A (PBMC1-iPS4F1)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal

  429. GENYOi003-A (PBMC2-iPS4F8)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal

  430. GENYOi004-A (ASD-PBMC-iPS4F2)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Adnp syndrome

  431. GENYOi005-A (FPD/AML-PBMC-iPSC4F73)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Familial platelet disorder with associated myeloid malignancy

  432. WAe009-A-7 (H9-mHOXA9)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Normal

  433. WAe009-A-60 (H9 iNK5A)

    Spain Centre for Genomics and Oncological Research (GENYO)
    Disease:

    Childhood acute myeloid leukemia

  434. WAe001-A-73 (H1-GATAD2B-KO-79#)

    China Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences (GIBH)
    Disease:

    Intellectual disability

  435. WAe001-A-76 (H1-RNF1-/-)

    China Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences (GIBH)
    Disease:

    Parkinson's disease

  436. WAe009-A-45

    China gynaecology and obstetrics, Anzhen Hospital (GOAH)
    Disease:

    Holt-oram syndrome

  437. GUCASe001-A (hPES-1)

    China Graduate University of Chinese Academy of Sciences (GUCAS)

  438. GZHMCe001-A (FY-hES-5)

    China The Third Affiliated Hospital of Guangzhou Medical University (GZHMC)
    Disease:

    Patau syndrome

  439. HADe003-A (HAD 3)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Factor viii deficiency

  440. HADe004-A (HAD 4)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Familial dysautonomia

  441. HADe007-A (HAD-C 100)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  442. HADe008-A (HAD-C 102)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  443. HADe009-B (HAD-C 106 Single-cell, Feeder-free (Seed Cell Bank, SCB))

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  444. HADe011-A (HAD-C 104 cGMP-grade, xeno-free Single-cell, Feeder-free Master Cell Bank)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  445. HADe012-A (HAD-C 105 cGMP-grade, xeno-free Single-cell, Feeder-free Master Cell Bank)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  446. HADe013-A (HAD-C 107 cGMP-grade, xeno-free Single-cell, Feeder-free Master Cell Bank)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  447. HEBHMUi010-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal

  448. HEBHMUi013-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Alzheimer's disease

  449. HELPi001-A (BS-TL-1)

    China Help Stem Cell Innovations Co.Ltd. (HELP)
    Disease:

    Congenital contractural arachnodactyly

  450. HHUUKDi001-A (ISRM-UM51 and UM51-iPSC)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Normal

  451. HHUUKDi009-A (TFBJ)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Normal

  452. HHUUKDi011-A (AATD iPSC-1 and ISRM-AATD-iPSC-1)

    Germany Heinrich-Heine-Universität Düsseldorf (HHUUKD)
    Disease:

    Alpha-1 antitrypsin deficiency

  453. HKUi002-A (AYC12 and HKUi002-A-AYC12)

    Hong Kong The University of Hong Kong (HKU)
    Disease:

    Dilated cardiomyopathy

  454. HMGUi001-A (XM001 and BIHi043-A)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Normal

  455. HMGUi002-A (XM002)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Normal

  456. HMSCATi001-A

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Normal

  457. HMSCATi003-A

    China Stem Cell Application and Translation Laboratory (HMSCAT)
    Disease:

    Parkinson disease

  458. HNMUi003-A (iPS-UC1290)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  459. HNMUi009-A (iPS-UC1171)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  460. HNMUi010-A (iPS-AF091)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  461. HUBi001-A (HUB001Ai)

    Netherlands The Hubrecht Institute (HUB)
    Disease:

    Normal

  462. HVRDe001-A (HuES1)

    United States Harvard University (HVRD)

  463. HVRDe003-A (HuES3)

    United States Harvard University (HVRD)

  464. HVRDe005-A (HuES5)

    United States Harvard University (HVRD)

  465. HVRDe006-A (HuES6)

    United States Harvard University (HVRD)
    Disease:

    Normal

  466. HVRDe009-A (HuES9)

    United States Harvard University (HVRD)
    Disease:

    Normal

  467. HVRDe012-A (HuES12)

    United States Harvard University (HVRD)

  468. HVRDe013-A (HuES13)

    United States Harvard University (HVRD)

  469. HVRDe015-A (HuES15)

    United States Harvard University (HVRD)

  470. HVRDe017-A (HuES17)

    United States Harvard University (HVRD)

  471. IAIi001-A (IAIi001RSTS2-65-A)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  472. IAIi005-A (AC52)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Normal

  473. IAIi010-A (Kif5A 1847 C3)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Autosomal dominant spastic paraplegia type 10

  474. IBBISTi004-A (AS-GB clone 12)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  475. IBKMOLi002-A (CACNA1D L271H iPCs)

    Austria University of Innsbruck, Institute of Molecular Biology (IBKMOL)
    Disease:

    Autism spectrum disorder

    Disease:

    Hyperinsulinemic hypoglycemia

    Disease:

    Primary hyperaldosteronism

    Disease:

    Muscle hypotonia

  476. BIONi010-C-65 (BiONI010-C-O16)

    Germany Fraunhofer Institute for Biomedical Engineering IBMT (IBMT)
    Disease:

    Cystic fibrosis

  477. IBPi001-A (HPrF iPSCs 20A)

    Czech Republic Institute of Biophysics of the Czech Academy of Sciences (IBP)
    Disease:

    Normal

  478. ICANi001-A (CDGEN1.16)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Hypertrophic cardiomyopathy

  479. ICANi001-A-1 (CDGEN1.16.40.5)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Hypertrophic cardiomyopathy

  480. ICANi002-A (ICAN-403.3)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal

  481. ICANi002-A-1 (ICAN-FLNC42.1)

    France INSERM U1166-Institute of Cardiometabolism And Nutrition (ICAN)
    Disease:

    Normal

  482. ICGi002-A (DMD1_1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  483. ICGi002-B (DMD1_4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  484. ICGi002-C (DMD1_11)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Duchenne muscular dystrophy

  485. ICGi003-A (f3SMA3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Spinal muscular atrophy type 3

  486. ICGi005-A (iSMA40)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 1

  487. ICGi005-B (iSMA37)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 1

  488. ICGi006-A (m3SMA13)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 2

  489. ICGi006-B (m3SMA20)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Proximal spinal muscular atrophy type 2

  490. ICGi007-A (47Q-3Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  491. ICGi008-A (m55Alz-9L)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_alzheimer's disease

  492. ICGi008-B (m55Alz-15L)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_alzheimer's disease

  493. ICGi009-A (iTAF3-17 and iTAF3del17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  494. ICGi009-B (iTAF3del37 and iTAF3-37)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  495. ICGi013-A (iTAF13-26 and iTAF13del26)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  496. ICGi013-B (iTAF13del27 and iTAF13-27)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Intellectual disability

  497. ICGi014-A (2M_iALS)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  498. ICGi015-A

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  499. ICGi015-B

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  500. ICGi015-B-1 (m6.7pCyto-17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  501. ICGi017-A (TAF14dup10)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal

  502. ICGi018-A (iHD38Q-3)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  503. ICGi018-B (iHD38Q-2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  504. ICGi018-C (iHD38Q-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington's disease

  505. ICGi019-A (HCM1f6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  506. ICGi019-B (HCM1f33)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  507. ICGi020-A (ATP7bIL23f)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Wilson disease

  508. ICGi020-B (ATP7bIL24f)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Wilson disease

  509. ICGi021-A (K6-4f)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal

  510. ICGi021-A-1 (K6-4fpCyto-13)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Healthy

  511. ICGi022-A (K7-4Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal

  512. ICGi022-A-1 (SOD1-G128R_K7-4L-f and SOD1-G128R)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Amyotrophic lateral sclerosis

  513. ICGi022-A-2 (SOD1-D91A and SOD1-D91A_K7-4Lf)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Amyotrophic lateral sclerosis

  514. ICGi022-A-3 (K7-MYBPC3-N515del-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  515. ICGi023-A (PD45-6-1Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  516. ICGi025-A (iTAF11-4)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Developmental delay

  517. ICGi026-A

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Fragile x syndrome

  518. ICGi028-A (HCM4fm5.2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  519. ICGi029-A (HCM14fm6.2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hypertrophic cardiomyopathy

  520. ICGi032-A

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Fragile x syndrome

  521. ICGi033-A (77Q-17)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  522. ICGi033-B (77Q-9)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  523. ICGi033-C (77Q-20)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Huntington disease

  524. ICGi034-A (PD30-4-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  525. ICGi034-B (PD30-5-16)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  526. ICGi034-C (PD30-5-27)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Obsolete_parkinson's disease

  527. ICGi035-A (iCS-MAF1-1)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal

  528. ICGi036-A (FH 1.3.1S)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hyperlipoproteinemia, type iia

  529. ICGi037-A (FH 3.2.8T)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hyperlipoproteinemia, type iia

  530. ICGi038-A (FH 5.1.2Sh)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Hyperlipoproteinemia, type iia

  531. ICGi039-A (PD31-6)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal

  532. ICGi039-B (PD31-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal

  533. ICGi039-C (PD31-15)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Normal

  534. ICGi042-A (PD12-4Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  535. ICGi042-B (PD12-5Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  536. ICGi042-C (PD12-6Lm)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  537. ICGi043-A (LR-21)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  538. ICGi043-B (LR-2)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  539. ICGi043-C (LR-15)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  540. ICGi044-A (PD40-7)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  541. ICGi044-B (PD40-8)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  542. ICGi044-C (PD40-13)

    Russia Institute of Cytology and Genetics, Siberian Branch of Russian Academy of Sciences (ICG)
    Disease:

    Parkinson's disease

  543. ICNDXHi001-A

    China Innovation Center for Neurological Disorders, Xuanwu Hospital, National Clinical Research Center for Geriatric Diseases (ICNDXH)
    Disease:

    Frontotemporal dementia

  544. IDIBGIi001-A (GPG1-C23)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Normal

  545. IDIBGIi002-A (RB20234)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Brugada syndrome

  546. IDIBGIi003-A (​RB20235)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Brugada syndrome

  547. IDIBGIi004-A (RB20236)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Brugada syndrome

  548. IDIBGIi005-A (RB20237)

    Spain Institut d'Investigació Biomèdica de Girona Dr. Josep Trueta (IDIBGI)
    Disease:

    Normal

  549. HMGUi001-A-5 (ΔINK4 T2D risk region hiPSC)

    Germany Institute of Diabetes and Regeneration Research (IDR)
    Disease:

    Normal

  550. IDVi001-A (iPS-NR2E3-86)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinitis pigmentosa

  551. IDVi002-A (iPS-PRPF31-4138)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Normal

  552. IIMCBi003-A (K-Pic1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)
    Disease:

    Normal

  553. IIMCBi006-A (M-T1)

    Poland International Institute of Molecular and Cell Biology in Warsaw (IIMCB)

  554. TECHe001-A (I3)

    Israel Technion - Israel Institute of Technology (IIT)

  555. TECHe002-A (I4)

    Israel Technion - Israel Institute of Technology (IIT)

  556. TECHe003-A (I6)

    Israel Technion - Israel Institute of Technology (IIT)

  557. IMAGINi004-A (IMAGINE004)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal

  558. IMAGINi005-A (IMAGINE005)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal

  559. IMAGINi013-A (IMAGINE013)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal

  560. IMAGINi021-A (IMAGINE021)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal

  561. IMBAi001-A (SCCF-176J clone#1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  562. IMBAi001-B (SCCF-176J clone#2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  563. IMBAi002-A (SCCF-177J clone#8)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  564. IMBAi002-B (SCCF-177J clone#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  565. IMBAi002-C (SCCF-177J clone#6)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  566. IMBAi003-A (SCCF-178J clone#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  567. IMBAi003-B (SCCF-178J clone#6)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  568. IMBPASi001-A (iPSC-WFS1-#1)

    Poland Institute of Medical Biology of Polish Academy of Sciences (IMBPAS)
    Disease:

    Wolfram syndrome 1

  569. IMGTi001-B (iTAF5-32)

    Russia Research Institute of Medical Genetics, TNMRC (IMGT)
    Disease:

    Monosomy 22q13.3

  570. IMGTi003-A (iTAF6-6)

    Russia Research Institute of Medical Genetics, TNMRC (IMGT)
    Disease:

    Ring chromosome 13 syndrome

  571. IMHe009-A (OZ-1)

    Turkey ISTANBUL MEMORIAL HOSPITAL (IMH)
    Disease:

    Chromosomal disease

  572. IMHe012-A (NS-9)

    Turkey ISTANBUL MEMORIAL HOSPITAL (IMH)

  573. IMHe013-A (NS-10)

    Turkey ISTANBUL MEMORIAL HOSPITAL (IMH)

  574. INNDSUi003-A

    China Institute of Neuromuscular and Neurodegenerative Diseases, Shandong University (INNDSU)
    Disease:

    Becker muscular dystrophy

  575. INSAi002-A

    Portugal Instituto Nacional de Saude Ricardo Jorge (INSA)
    Disease:

    Fabry disease

  576. INSRMe013-A (STR-I-301-MFS)

    France INSERM (INSRM)
    Disease:

    Marfan syndrome

  577. IPTi001-A (15M0008)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  578. IPTi002-A (15F0009)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  579. IPTi003-A (15M0010)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  580. IPTi004-A (15M0011)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  581. IPTi005-A (16M0064)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal

  582. IPTi006-A (16M0065)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal

  583. IPTi007-A (16F0066)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal

  584. IRFMNi001-B-2 (CIone M CIITAKO-B2MKO)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Normal

  585. IRFMNi003-A-4 (KO PKD1#5)

    Italy IRCCS - Istituto di Ricerche Farmacologiche Mario Negri (IRFMN)
    Disease:

    Autosomal dominant polycystic kidney disease

  586. IRMBi001-A (AD-PS1 hiPSC)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Obsolete_alzheimer's disease

  587. IRMBi002-A (AD-APP hiPSC)

    France Institute for Regenerative Medecine and Biotherapy (IRMB)
    Disease:

    Obsolete_alzheimer's disease

  588. SNUe003-A-2 (B-mC-KI-SE-3)

    South Korea Institute of Reproductive Medicine and Population, Medical Research Cener, (IRMP)
    Disease:

    Normal

  589. SNUe003-A-3 (A-eG-KI-SE-3)

    South Korea Institute of Reproductive Medicine and Population, Medical Research Cener, (IRMP)
    Disease:

    Normal

  590. SNUe003-A-4 (T-mC-KI-SE-3)

    South Korea Institute of Reproductive Medicine and Population, Medical Research Cener, (IRMP)
    Disease:

    Normal

  591. SNUe004-A-2 (A-eG-KI-SE-4)

    South Korea Institute of Reproductive Medicine and Population, Medical Research Cener, (IRMP)
    Disease:

    Normal

  592. ISFi003-A (D2)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Van maldergem syndrome 1

  593. ISMMSi001-A (SAMEA104275576 and MFS44-E)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  594. ISMMSi001-B (SAMEA104275577 and MFS44-16)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  595. ISMMSi002-A (SAMEA104275578 and MFS60-12)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  596. ISMMSi002-B (MFS60-3-1 and SAMEA104276575)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Marfan syndrome

  597. ISMMSi004-A (MSN01-02S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal

  598. ISMMSi013-A (MSN10-07S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal

  599. ISMMSi023-A (MSN20-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal

  600. ISMMSi027-A (MSN24-06S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal

  601. ISMMSi035-A (MSN32-04S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal

  602. ISMMSi038-A (MSN35-05S)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal

  603. ISMMSi044-A (PLNR14del-1BC1)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  604. ISMMSi046-A (PLN-R14del-3BC7)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  605. ISMMSi048-A (PLN-R14del-5BC4)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Cardiomyopathy

  606. ISMMSi049-A (PLN-1CC1)

    United States Icahn School of Medicine at Mount Sinai (ISMMS)
    Disease:

    Normal

  607. ITXi001-A (hERG CT Cl9)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  608. ITXi003-A (MS368)

    France l’institut du thorax (ITX)
    Disease:

    Long qt syndrome

  609. ITXi007-A (202CT)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  610. ITXi008-A (SD378M)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  611. IUFi002-A

    Germany IUF – Leibniz Research Institute for Environmental Medicine (IUF)
    Disease:

    Leigh syndrome

  612. JNCSRe001-A (BJNhem19)

    India Jawaharlal Nehru Centre for Advanced Scientific Research (JNCSR)

  613. JNCSRe002-A (BJNhem20)

    India Jawaharlal Nehru Centre for Advanced Scientific Research (JNCSR)
    Disease:

    Normal

  614. JNCSRe002-A-2 (BJNhem20-OCIAD2-CRISPR-40)

    India Jawaharlal Nehru Centre for Advanced Scientific Research (JNCSR)
    Disease:

    Normal

  615. JTUi001-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Charge syndrome

  616. JTUi002-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Waardenburg syndrome

  617. JTUi005-A

    China Sixth People's Hospital, Shanghai Jiao Tong University (JTU)
    Disease:

    Neuronal intranuclear inclusion disease

  618. KAUSTi001-A (KS7-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  619. KAUSTi001-B (KS7-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  620. KAUSTi003-A (KS1-iPSC#D)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  621. KAUSTi004-A (HM-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  622. KAUSTi004-B (HM-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  623. KAUSTi005-A (HB-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  624. KAUSTi005-B (HB-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  625. KAUSTi005-C (HB-iPSC#C)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  626. KAUSTi006-A (KS6-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  627. KAUSTi006-B (KS6-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  628. KAUSTi007-A (KS2-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  629. KAUSTi007-B (KS2-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  630. KAUSTi008-A (KS4-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  631. KAUSTi008-B (KS4-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  632. KAUSTi008-C (KS4-iPSC#C)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  633. KAUSTi008-D (KS4-iPSC#D)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  634. KAUSTi008-E (KS4-iPSC#E)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  635. KAUSTi008-F (KS4-iPSC#F)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  636. KAUSTi008-G (KS4-iPSC#G)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  637. KAUSTi009-A (KS3-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  638. KAUSTi009-B (KS3-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  639. KAUSTi010-A (KS5-iPSC#A)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  640. KAUSTi010-B (KS5-iPSC#B)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Klinefelter's syndrome

  641. KAUSTi011-A (iPSC-GLP1R-KO-C1)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Developmental and epileptic encephalopathy

  642. KAUSTi011-B (iPSC-GLP1R-KO-H4)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Developmental and epileptic encephalopathy

  643. WAe001-A-82 (H1X-59 and H1X59)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  644. WAe001-A-83 (H1.0-29 and H1.029)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  645. WAe001-A-84 (H1.117 and H1.1-17)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  646. WAe001-A-85 (H1.0102 and H1.0-102)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  647. WAe001-A-87 (H1.213 and H1.2-13)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  648. WAe001-A-88 (H1.2-124 and H1.2124)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  649. WAe001-A-89 (H1.3-64 and H1.364)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  650. WAe001-A-90 (H1.3-191 and H1.3191)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  651. WAe001-A-91 (H1.4-126 and H1.4126)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  652. WAe001-A-92 (H1.4-143 and H1.4143)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  653. WAe001-A-93 (H1.5-23 and H1.523)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  654. WAe001-A-94 (H1.528 and H1.5-28)

    Saudi Arabia King Abdullah University of Science and Technology (KAUST)
    Disease:

    Normal

  655. KCLe009-A (KCL012_HD3)

    United Kingdom King's College London (KCL)
    Disease:

    Huntington disease

  656. KCLe010-A (KCL013_HD4)

    United Kingdom King's College London (KCL)
    Disease:

    Huntington disease

  657. KCLe011-A (KCL015_VHL2)

    United Kingdom King's College London (KCL)
    Disease:

    Von hippel-lindau disease

  658. KCLe012-A (KCL016_VHL3)

    United Kingdom King's College London (KCL)
    Disease:

    Von hippel-lindau disease

  659. KCLe013-A (KCL017_VHL4)

    United Kingdom King's College London (KCL)
    Disease:

    Von hippel-lindau disease

  660. KCLe014-A (KCL018_MD1)

    United Kingdom King's College London (KCL)
    Disease:

    Myotonic dystrophy type 1

  661. KCLe015-A (KCL011)

    United Kingdom King's College London (KCL)

  662. KGUi001-A (AR1023)

    Germany Department of Psychiatry, Psychotherapy and Psychosomatic Medicine, University Hospital, Goethe University of Frankfurt/Main (KGU)
    Disease:

    Obsolete_bipolar disorder

  663. KIe001-A-1

    Sweden Karolinska Institutet (KI)
    Disease:

    Normal

  664. KIe007-A (HS346)

    Sweden Karolinska Institutet (KI)

  665. KIe013-A (HS364)

    Sweden Karolinska Institutet (KI)

  666. KIe013-A-1

    Sweden Karolinska Institutet (KI)

  667. KIe019-A (HS401)

    Sweden Karolinska Institutet (KI)

  668. KIe022-A (HS420)

    Sweden Karolinska Institutet (KI)

  669. WAe009-A-99 (dCas9-p300 H9 21)

    South Korea Korea Institute of Toxicology (KIT)
    Disease:

    Normal

  670. KLRMMEi001-A

    China Key Laboratory for Regenerative Medicine of Ministry of Education, Jinan University. (KLRMME)
    Disease:

    Retinitis pigmentosa

  671. KMUGMCi002-A (KMUGMCi002NIPBL)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Cornelia de lange syndrome

  672. KMUGMCi004-A (KMUGMCi004APC and KN615)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Familial adenomatous polyposis

  673. KRIBBi005-A (CB-iPS-C7)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    Normal

  674. WAe009-A-95 (hTRF1-KO #3)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    Normal

  675. WAe009-A-96 (hTRF1-KO #6)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    None

  676. WAe009-A-97 (hTRF1-KO #9)

    South Korea Korea Research Institute of Bioscience and Biotechnology (KRIBB)
    Disease:

    None

  677. KSCBi001-A (hUSiPS2)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal

  678. KSCBi003-A (hAdMSiPS1 and hAdMSCiPS1)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal

  679. KSCBi005-A-3 (CMC-003i-Pdx1.EGFP and CMC-hiPSC-003(PDX1-GFP))

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal

  680. KSCBi006-A (KNIH-OI001i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Osteogenesis imperfecta type 1

  681. KSCBi007-A (KNIH-PWS001i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Prader-willi syndrome

  682. KSCBi010-A (DKH005i-A and DKHi005-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Senior-loken syndrome

  683. KSCBi011-A (DKHi090-A and DKH090i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Leber congenital amaurosis

  684. KUe013-A (LRB016)

    Denmark University of Copenhagen (KU)

  685. KUIFMSi004-A (201B1)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  686. KUIFMSi004-B (201B6)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  687. KUIFMSi004-C (201B7)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  688. KUIFMSi004-D (201B2)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  689. KUIFMSi004-E (201B3)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  690. KUIFMSi009-A (243H1)

    Japan Kyoto University (KUIMS)

  691. KUIFMSi009-B (243H7)

    Japan Kyoto University (KUIMS)

  692. KUIFMSi011-A (246G1)

    Japan Kyoto University (KUIMS)

  693. KUIFMSi011-B (246G3)

    Japan Kyoto University (KUIMS)

  694. KUIFMSi011-C (246G4)

    Japan Kyoto University (KUIMS)

  695. KUIFMSi011-D (246G5)

    Japan Kyoto University (KUIMS)

  696. KUIFMSi011-E (246G6)

    Japan Kyoto University (KUIMS)

  697. KUMi002-A (CD34+ CML (Ph-) hiPSCs)

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Chronic myeloid leukemia

  698. KUMi003-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Acute promyelocytic leukemia

  699. KUMi004-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Chronic lymphocytic leukemia

  700. KUMi005-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Multiple myeloma

  701. KUMi006-A

    South Korea Korea University Medical School Hospital (KUM)
    Disease:

    Multiple myeloma

  702. KUMCi001-A (ALLCD34+)

    South Korea KOREA UNIVERSTY COLLEGE OF MEDICINE (KUMC)
    Disease:

    Acute lymphoblastic leukemia

  703. KUMCi002-A (MM_CD34+iPSCs)

    South Korea KOREA UNIVERSTY COLLEGE OF MEDICINE (KUMC)
    Disease:

    Multiple myeloma

  704. CHAHESe001-A-1 (CHA-hES NT6 B2M KO#67)

    South Korea Konkuk University (KUSCRB)
    Disease:

    Age-related macular degeneration

  705. LCPHi001-A

    China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)
    Disease:

    Obsolete_parkinson's disease

  706. LCPHi002-A

    China The Institute for Tissue Engineering and Regenerative Medicine, Liaocheng People's Hospital (LCPH)
    Disease:

    Parkinson's disease

  707. LCSBi002-C (ND40066-clone 8 and ND40066-PINK1/PARK6-ILE368ASN-clone 8)

    United States Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson's disease

  708. LCSBi004-A (ND29369-clone 1 and ND29369-PARKIN/PRKN/PARK2-R275W-clone 1)

    United States Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson's disease

  709. LCSBi004-B (ND29369-PARKIN/PRKN/PARK2-R275W-clone 4, ND29369-clone 4, ND29369-4 and LCSBi004-B)

    United States Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson's disease

  710. LEIi004-A

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  711. LEIi004-A-1