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  1. AHQUi001-A (IPS35-2)

    China Affiliated Hospital of Qingdao University (AHQU)
    Disease:

    Non rare in europe: hyperlipoproteinemia type 4

  2. AMUFAHi001-A

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

    Normal

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

    China Anzhen Hospital (ANZHEN)
    Disease:

    Hypertrophic cardiomyopathy

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Normal

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 1 diabetes mellitus

  7. ASGRCi004-A (0118 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Proliferative diabetic retinopathy

    Disease:

    Type 2 diabetes mellitus

  8. ASGRCi005-A (0622 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Keratoconjunctivitis sicca

  9. ASGRCi006-A (0808 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Proliferative diabetic retinopathy

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

  11. BCHNi001-A (BCHi001-A)

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

    Bardet-biedl syndrome

  12. BCHNCi001-A

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

    Early infantile epileptic encephalopathy

  13. BFVSBi001-A

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

    Arterial calcification

  14. BGUi002-A (BGU02iPOR)

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

    P450 oxidoreductase deficiency

  15. BGUi003-A (BGU03iPOR)

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

    P450 oxidoreductase deficiency

  16. BGUi004-A (BGU101iCCHS)

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

    Congenital central hypoventilation syndrome

  17. BGUi005-A (BGU102iCCHS)

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

    Congenital central hypoventilation syndrome

  18. BGUi008-A (DCM-C)

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

    Left ventricular noncompaction cardiomyopathy

  19. BGUi009-A (DCM-O)

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

    Left ventricular noncompaction cardiomyopathy

  20. BGUi010-A (DCM-R)

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

    Left ventricular noncompaction cardiomyopathy

  21. BGUi011-A (BGU01iGRIN2D)

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

    Developmental and epileptic encephalopathy, 46

  22. BGUi012-A (BGU02iGRIN2D CTR)

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

    Normal

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  24. BIHi001-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  25. BIHi002-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Autosomal recessive osteopetrosis 4

  26. BIHi004-B (NHDF Epi5 Cl2 iPSC)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  27. BIHi005-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  28. BIHi005-A-5

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_alzheimer's disease

  29. BIHi006-D

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  30. BIHi007-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  31. BIHi008-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  32. BIHi009-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  33. BIHi010-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  34. BIHi011-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  35. BIHi012-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  36. BIHi015-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  37. BIHi016-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  38. BIHi017-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  39. BIHi018-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  40. BIHi019-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  41. BIHi024-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  42. BIHi025-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  43. BIHi028-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  44. BIHi029-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  45. BIHi030-C

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  46. BIHi031-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  47. BIHi032-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  48. BIHi038-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  49. BIHi250-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  50. BIHi266-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  51. BIHi267-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

  52. BIHi269-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  53. BIHi276-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

  54. BIOi002-A

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Autosomal dominant optic atrophy

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

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Hereditary retinal dystrophy

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

    Denmark Bioneer (BION)
    Disease:

    Normal

  57. STBCi006-A-1 (ApoE KO)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

  60. BIONi010-A (K1P53)

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Inflammatory disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

  89. BIONi016-A (H310715 47-1)

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

  105. BIONi033-A (H180615 and SAMEA4563389)

    Denmark Bioneer (BION)
    Disease:

    Normal

  106. BIONi034-A (H290715 and SAMEA4563391)

    Denmark Bioneer (BION)
    Disease:

    Normal

  107. BIONi035-A (H180815 and SAMEA4563393)

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Hungary BioTalentum Ltd. (BIOT)
    Disease:

    Obsolete_alzheimer's disease

  109. BIUi001-A (T1A1i-001)

    Israel Bar Ilan University (BIU)
    Disease:

    Obsolete: nuclear cell envelopathy

  110. BIUi002-A (T1A1i-002)

    Israel Bar Ilan University (BIU)
    Disease:

    Obsolete: nuclear cell envelopathy

  111. BJTTHi001-A

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Normal

  112. BJTTHi001-A-1

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  113. BJTTHi001-A-2

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Dravet syndrome

    Disease:

    Epilepsy

  114. BJTTHi001-A-3

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  115. BJTTHi001-A-4

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  116. BJTTHi001-A-5

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  117. BRCi021-A (TUH1)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Cardiomyopathy

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

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

    Retinitis pigmentosa

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

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

    Age-related macular degeneration

  120. CBi001-A (XLC-348)

    United States Creative Bioarray (CB)
    Disease:

    Obsolete_schizophrenia

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

    United States Creative Bioarray (CB)
    Disease:

    Obsolete_schizophrenia

  122. CBIGi001-A (AIW002-02)

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

    Normal

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Normal

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Normal

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

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

    Myotonic dystrophy type 1

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

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

    Normal

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

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

    Normal

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

    Austria St. Anna Kinderkrebsforschung GmbH (CCRI)
    Disease:

    Normal

  137. CEBe033-A (SA001)

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

    Normal

  138. CENSOi001-B (FB78R2c2 and CENSOi249)

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

    Duchenne muscular dystrophy

  139. CENSOi002-B (FB74R2c4 and CENSOi261)

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

    Duchenne muscular dystrophy

  140. CENSOi003-B (FB79R2c6 and CENSOi258)

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

    Duchenne muscular dystrophy

  141. CENSOi005-A (FB76R2c5 and CENSOi245)

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

    Duchenne muscular dystrophy

  142. CENSOi007-A (FB75R2c5 and CENSOi255)

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

    Duchenne muscular dystrophy

  143. CENSOi008-A (FB77R2c3 and CENSOi260)

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

    Myotonic dystrophy type 1

  144. CHAe002-A (CHA-hES4)

    South Korea Pochon CHA University (CHA)

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

    South Korea CHA University (CHAHES)
    Disease:

    Age-related macular degeneration

  146. CHCMUi001-A

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

    Activated pi3k-delta syndrome

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal

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

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

    Myotonic dystrophy type 1

  193. CIPi001-A

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

    Benign familial infantile epilepsy

  194. CIPi002-A

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

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

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

    Facioscapulohumeral muscular dystrophy 2

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

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

    Facioscapulohumeral muscular dystrophy 2

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

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

    Facioscapulohumeral muscular dystrophy 2

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

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

    Facioscapulohumeral muscular dystrophy 2

  199. CMCi011-A (CMC-DENT-001)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Dent disease

  200. CMGANTi003-A (SEMD1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  201. CMGANTi004-A (SEMD2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  202. CMUi002-A

    China Capital Medical University (CMU)
    Disease:

    Normal

  203. CMUi002-A-1 (NONO-KO-iPSCs)

    China Capital Medical University (CMU)
    Disease:

    Left ventricular noncompaction cardiomyopathy

    Disease:

    Mental retardation

  204. CPGHi004-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal

  205. CPGHi006-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Autosomal dominant polycystic kidney disease

  206. CPGHi007-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal

  207. CPGHi008-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Autosomal recessive polycystic kidney disease

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

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

    X-linked centronuclear myopathy

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

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

    Normal

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

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

    Normal

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

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

    Normal

  212. CRTDi003-A (CRTD2)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  213. CRTDi003-B (CRTD3)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  214. CRTDi004-A (CRTD1)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  215. CRTDi005-A (CRTD4)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  216. CRTDi005-B (CRTD5)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  217. CRTDi006-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  218. CRTDi006-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  219. CRTDi007-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  220. CRTDi007-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  221. CRTDi008-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  222. CRTDi009-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  223. CRTDi010-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  224. CRTDi011-A (IDP52555 #9)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  225. CRTDi011-B (IDP52555 #13)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  226. CRTDi011-C (IDP52555 #36)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  227. CRTDi011-D (IDP52555 #44)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  228. CSSi016-A

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

    Charcot-marie-tooth disease type 4b3

  229. CSUe004-A (chHES-20)

    China Central South University (CSU)

  230. CSUe005-A (chHES-22)

    China Central South University (CSU)

  231. CSUXHi003-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Waardenburg syndrome type 2

  232. CSUXHi004-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Waardenburg syndrome type 1

  233. CUIMCi004-A (1514_1)

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

    Class 3 obesity

  234. CVTTHi001-A

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

    Activated pi3k-delta syndrome

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

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

    Normal

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

  239. DANi005-A (LRRK2-GBA-005-C1)

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

    Parkinson's disease

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

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

    Parkinson's disease

  241. DANi007-A (PINK1-007-C1)

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

  246. DMBi001-A-2

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Normal

  247. DRICUi003-A (LC56A10005A)

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

    Late-onset alzheimers disease

  248. DRICUi004-A (LC56A10012A)

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

    Late-onset alzheimers disease

  249. DRICUi005-A (LW44A10001A)

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

    Late-onset alzheimers disease

  250. DRICUi006-A (ADANG10496CA)

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

    Late-onset alzheimers disease

  251. DRICUi007-A (ADANG10605CA)

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

    Late-onset alzheimers disease

  252. DRICUi009-A (ADLON44426UC)

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

    Normal

  253. DRICUi010-A (BS38A10004A)

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

    Late-onset alzheimers disease

  254. DRICUi011-A (BS38A10002A)

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

    Late-onset alzheimers disease

  255. DRICUi012-A (NT18A10014A)

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

    Late-onset alzheimers disease

  256. DRICUi013-A (SC45A10021A)

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

    Late-onset alzheimers disease

  257. DRICUi014-A (CF00C90323A)

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

    Normal

  258. WAe009-A-58 (COL4A5 heterozygote)

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

    Alport syndrome

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

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

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

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

  261. 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

  262. 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

  263. 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

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

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  265. EDi010-A (RCi136)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  266. EDi010-B (RCi138)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  267. EDi011-A (RCi139)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  268. EDi011-B (RCi140)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  269. EDi011-C (RCi141)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  270. EDi012-A (RCi163)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  271. EDi012-B (RCi164)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  272. EDi012-C (RCi165)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  273. EDi013-A (RCi192)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  274. EDi013-B (RCi193)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  275. EDi013-C (RCi214)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  276. EDi014-A (RCi175)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Unipolar depression

    Disease:

    Anti-social behavior

  277. EDi014-B (RCi185)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Unipolar depression

    Disease:

    Anti-social behavior

  278. EDi015-A (RCi176)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Unipolar depression

  279. EDi015-B (RCi183)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Unipolar depression

  280. EDi015-C (RCi184)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Unipolar depression

  281. EDi016-A (RCi189)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  282. EDi016-C (RCi191)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  283. EDi017-A (RCi174)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  284. EDi017-B (RCi181)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  285. EDi017-C (RCi182)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  286. EDi018-A (RCi211)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  287. EDi018-B (RCi212)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  288. EDi018-C (RCi213)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  289. EDi019-A (RCi166)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  290. EDi019-B (RCi167)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  291. EDi019-C (RCi168)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  292. EDi022-A (CS0617iCTR-LBCn1)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  293. EDi023-A (CS0791iCTR-LBCn1)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  294. EDi037-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  295. EDi038-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  296. EDi040-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  297. EDi041-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  298. EDi042-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  299. EDi043-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  300. EDi044-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

  301. EDi045-A

    United States University of Edinburgh (ED)
    Disease:

    Normal

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

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

    Normal

  303. ESi001-A (SPO2#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  304. ESi002-A (SP08#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  305. ESi003-A ([CRTRd]FiPS3819-4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    X-linked creatine transporter deficiency

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Fanconi anemia

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Fanconi anemia

  308. ESi006-A (SP13#4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  310. ESi008-B (KiPS3F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  312. ESi035-A (AD]FiPSAG07645-4F-17)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_alzheimer's disease

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_parkinson's disease

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  322. ESi045-A (FiPS Ctrl2-mR5F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  324. ESi045-C (FiPS Ctrl2-SV4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  325. ESi045-D (FiPS Ctrl2-R4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_multiple sclerosis

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

  333. ESi054-A (AS FiPS 1-Ep6F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Alport syndrome

  334. ESi055-A (AS FiPS 2-Ep6F-28)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Alport syndrome

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Alport syndrome

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_type i diabetes mellitus

  345. ESi068-A (SWB FiPS 159-R4F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams-beuren syndrome

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams-beuren syndrome

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsessive-compulsive disorder

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsessive-compulsive disorder

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiotoxicity

  352. ESi075-A (BST PBiPS1-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Retinitis pigmentosa

  355. ESi078-A (cPRPF31-MiPS4F7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  356. ESi079-A (cAMDdh09-MiPS4F17)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  358. ESi081-A (SP11#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  359. ESi082-A (CRB1-MiPS4F1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Macular degeneration

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  361. ESi091-A (HLA91-MiPS4F3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  362. ESi092-A (HLA98-MiPS4F15)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  363. ESi093-A (CD34 iPS1-Sv4F-B8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  364. ESi094-A (Hz 1-8-3 CBiPS4 Sv4F F6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  365. ESi095-A (Hz 3-7-15 CBiPS3- Sv4F E9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  366. ESi096-A (Hz 11-27-1 CBiPS8-Sv4F-J1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  367. ESi097-A (Hz 24-7-15 CBiPS7 Sv4F-I12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  368. ESi098-A (Hz 30-18-3 CBiPS2-Sv4F-D10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  369. ESi099-A (Hz 33-14-1 CBiPS6-Sv4F H6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  370. ESi100-A (NW FiPS 10II.3-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  371. ESe009-A (ES-2)

    Spain Spanish Stem Cell Bank (ES)

  372. ESe010-A (ES-3)

    Spain Spanish Stem Cell Bank (ES)

  373. ESIBIe002-A (HES-2)

    Singapore ES Cell International Pte Ltd. (ESIBI)
    Disease:

    Normal

  374. ESIBIe003-A (HES-3 and hES 3)

    Singapore ES Cell International Pte Ltd. (ESIBI)
    Disease:

    Normal

  375. WAe009-A-43

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

    Long qt syndrome

  376. 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

  377. 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

  378. FAMRCi005-A (LMNA B4)

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

    Paroxysmal ventricular tachycardia

    Disease:

    Atrioventricular block

    Disease:

    Myopathy

  379. FAMRCi005-B (LMNA B5)

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

    Paroxysmal ventricular tachycardia

    Disease:

    Atrioventricular block

    Disease:

    Myopathy

  380. FAMRCi006-A (LMNA T3)

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

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  381. FAMRCi006-B (LMNA T4)

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

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  382. 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

  383. 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

  384. FAMRCi009-A (RCMP43)

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

    Restrictive cardiomyopathy

  385. FAMRCi010-A (RCMP48)

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

    Restrictive cardiomyopathy

  386. FDCHi004-A (iPS-39)

    China Children’s Hospital of Fudan University (FDCH)
    Disease:

    Osteogenesis imperfecta

  387. FDCHDPi001-A (FDCHDP01)

    China Fudan University (FDCHDP)
    Disease:

    Tourette syndrome

  388. FDHPIi001-A

    China (WITHDRAWN) Fudan University (FDHPI)
    Disease:

    Neurodegeneration

  389. FINi002-A (FI.CPLT.PRKN.R275W+del_e8.PK006)

    Australia The Florey Institute of Neuroscience and Mental Health (FIN)
    Disease:

    Parkinson's disease

  390. FJMUUHi001-A

    China Fujian Medical University Union Hospital (FJMUUH)
    Disease:

    Parkinson's disease 7

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

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

    Normal

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

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

    Normal

  393. 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

  394. FRIMOi001-A (RP1_FiPS4F1.6)

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

    Retinitis pigmentosa

  395. FRIMOi002-A (RP2_FiPS4F2.2)

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

    Retinitis pigmentosa

  396. FRIMOi003-A (STGD1_ FiPS4F1.5)

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

    Stargardt disease

  397. FRIMOi004-A (STGD2_ FiPS4F1.7)

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

    Stargardt disease

  398. FRIMOi005-A (RP3_FiPS4F11)

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

    Retinitis pigmentosa

  399. FRIMOi006-A (BEST1_FiPS4F1)

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

    Bestrophinopathy

  400. FRIMOi007-A (PDE6C_FiPS4F1)

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

    Achromatopsia

  401. GENEAe016-A (GENEA022)

    Australia Genea (GENEA)
    Disease:

    Normal

  402. GENEAe017-A (GENEA023)

    Australia Genea (GENEA)
    Disease:

    Normal

  403. GENEAe021-A (GENEA021)

    Australia Genea (GENEA)
    Disease:

    Normal

  404. GENYOi001-A (PBMC1-iPS4F1)

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

    Normal

  405. GENYOi003-A (PBMC2-iPS4F8)

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

    Normal

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

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

    Adnp syndrome

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

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

    Familial platelet disorder with associated myeloid malignancy

  408. GENYOi006-A (GRX-MCiPS4F-A2)

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

    Normal

  409. GENYOi006-A-1 (GRX-MCiPS4F-A2-ETO2-GLIS2)

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

    Acute myeloid leukemia

  410. GENYOi006-A-2 (GRX-MCiPS4F-A2-NEO)

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

    Normal

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

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

    Normal

  412. WAe009-A-60 (H9 iNK5A)

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

    Childhood acute myeloid leukemia

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

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

    Intellectual disability

  414. WAe009-A-84

    China Guangxi Institute of Cardiovascular Diseases (GICD)
    Disease:

    Congenital heart disease

  415. WAe009-A-45

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

    Holt-oram syndrome

  416. GUCASe001-A (hPES-1)

    China Graduate University of Chinese Academy of Sciences (GUCAS)

  417. GWCMCi001-A (iPS-57)

    China Guangzhou Women and Children's Medical Center (GWCMC)
    Disease:

    Iga glomerulonephritis

  418. HADe005-A (HAD 5)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Fragile x syndrome

  419. HDZi001-A (hiPSC NP0039)

    Germany Heart and Diabetes Center North Rhine Westphalia (HDZ)
    Disease:

    Arrhythmogenic right ventricular dysplasia 5

  420. HEBHMUi009-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Obsolete_alzheimer's disease

  421. HEBHMUi011-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Obsolete_alzheimer's disease

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

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

    Congenital contractural arachnodactyly

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

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

    Dilated cardiomyopathy

  424. HMSCATi002-A

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

    Normal

  425. HMSCATi003-A

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

    Parkinson disease

  426. WAe009-A-N

    China Henan Provincial Chest Hospital (HPCH)
    Disease:

    Inflammatory bowel disease

  427. HUBi001-A (HUB001Ai)

    Netherlands The Hubrecht Institute (HUB)
    Disease:

    Normal

  428. HUJIe001-A (HEFX1)

    Israel Hebrew University of Jerusalem (HUJI)
    Disease:

    Fragile x syndrome

  429. HVRDe001-A (HuES1)

    United States Harvard University (HVRD)

  430. HVRDe003-A (HuES3)

    United States Harvard University (HVRD)

  431. HVRDe005-A (HuES5)

    United States Harvard University (HVRD)

  432. HVRDe006-A (HuES6)

    United States Harvard University (HVRD)
    Disease:

    Normal

  433. HVRDe009-A (HuES9)

    United States Harvard University (HVRD)
    Disease:

    Normal

  434. HVRDe012-A (HuES12)

    United States Harvard University (HVRD)

  435. HVRDe015-A (HuES15)

    United States Harvard University (HVRD)

  436. HVRDe017-A (HuES17)

    United States Harvard University (HVRD)

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

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  438. 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

  439. IBPi001-A (HPrF iPSCs 20A)

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

    Normal

  440. IBPi002-A (P71 iPSCs 1)

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

    Prostate adenocarcinoma

  441. ICANi001-A (CDGEN1.16)

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

    Hypertrophic cardiomyopathy

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

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

    Hypertrophic cardiomyopathy

  443. ICANi002-A (ICAN-403.3)

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

    Normal

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

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

    Normal

  445. ICGi002-A (DMD1_1)

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

    Duchenne muscular dystrophy

  446. ICGi002-B (DMD1_4)

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

    Duchenne muscular dystrophy

  447. ICGi002-C (DMD1_11)

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

    Duchenne muscular dystrophy

  448. ICGi003-A (f3SMA3)

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

    Spinal muscular atrophy type 3

  449. ICGi005-A (iSMA40)

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

    Proximal spinal muscular atrophy type 1

  450. ICGi005-B (iSMA37)

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

    Proximal spinal muscular atrophy type 1

  451. ICGi006-A (m3SMA13)

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

    Proximal spinal muscular atrophy type 2

  452. ICGi006-B (m3SMA20)

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

    Proximal spinal muscular atrophy type 2

  453. ICGi008-A (m55Alz-9L)

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

    Obsolete_alzheimer's disease

  454. ICGi008-B (m55Alz-15L)

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

    Obsolete_alzheimer's disease

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

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

    Intellectual disability

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

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

    Intellectual disability

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

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

    Intellectual disability

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

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

    Intellectual disability

  459. ICGi014-A (2M_iALS)

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

    Obsolete_amyotrophic lateral sclerosis

  460. ICGi015-A

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

    Parkinson's disease

  461. ICGi015-B

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

    Parkinson's disease

  462. ICGi016-A (iTaf9-11)

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

    Mental retardation, autosomal dominant 39

  463. ICGi018-A (iHD38Q-3)

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

    Huntington's disease

  464. ICGi018-B (iHD38Q-2)

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

    Huntington's disease

  465. ICGi018-C (iHD38Q-1)

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

    Huntington's disease

  466. ICGi019-A (HCM1f6)

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

    Hypertrophic cardiomyopathy

  467. ICGi019-B (HCM1f33)

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

    Hypertrophic cardiomyopathy

  468. ICGi021-A (K6-4f)

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

    Normal

  469. ICGi022-A (K7-4Lf)

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

    Normal

  470. 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

  471. 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

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

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

    Parkinson's disease

  473. ICGi024-A

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

    Ring chromosome 18 syndrome

  474. ICGi026-A

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

    Fragile x syndrome

  475. ICGi028-A (HCM4fm5.2)

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

    Hypertrophic cardiomyopathy

  476. ICGi029-A (HCM14fm6.2)

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

    Hypertrophic cardiomyopathy

  477. ICGi032-A

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

    Fragile x syndrome

  478. ICGi033-A (77Q-17)

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

    Huntington disease

  479. ICGi033-B (77Q-9)

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

    Huntington disease

  480. ICGi033-C (77Q-20)

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

    Huntington disease

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

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

    Obsolete_parkinson's disease

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

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

    Obsolete_parkinson's disease

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

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

    Obsolete_parkinson's disease

  484. ICGi036-A (FH 1.3.1S)

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

    Hyperlipoproteinemia, type iia

  485. ICGi037-A (FH 3.2.8T)

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

    Hyperlipoproteinemia, type iia

  486. ICGi038-A (FH 5.1.2Sh)

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

    Hyperlipoproteinemia, type iia

  487. ICGi039-A (PD31-6)

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

    Normal

  488. ICGi039-B (PD31-7)

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

    Normal

  489. ICGi039-C (PD31-15)

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

    Normal

  490. ICGi040-A (iTAF16-3)

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

    Infertility

  491. ICGi042-A (PD12-4Lm)

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

    Parkinson's disease

  492. ICGi042-B (PD12-5Lm)

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

    Parkinson's disease

  493. ICGi042-C (PD12-6Lm)

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

    Parkinson's disease

  494. ICGi043-A (LR-21)

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

    Parkinson's disease

  495. ICGi043-B (LR-2)

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

    Parkinson's disease

  496. ICGi043-C (LR-15)

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

    Parkinson's disease

  497. ICGi044-A (PD40-7)

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

    Parkinson's disease

  498. ICGi044-B (PD40-8)

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

    Parkinson's disease

  499. ICGi044-C (PD40-13)

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

    Parkinson's disease

  500. ICNDXHi001-A

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

    Frontotemporal dementia

  501. IDIBGIi001-A (GPG1-C23)

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

    Normal

  502. IDIBGIi002-A (RB20234)

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

    Brugada syndrome

  503. IDIBGIi003-A (​RB20235)

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

    Brugada syndrome

  504. IDIBGIi004-A (RB20236)

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

    Brugada syndrome

  505. IDIBGIi005-A (RB20237)

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

    Normal

  506. IDISi001-A

    Spain Health Research Institute of Santiago de Compostela (IDIS)
    Disease:

    Cerebral autosomal dominant arteriopathy-subcortical infarcts-leukoencephalopathy

  507. IIMCBi004-A (PM-H1)

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

  508. TECHe001-A (I3)

    Israel Technion - Israel Institute of Technology (IIT)

  509. TECHe002-A (I4)

    Israel Technion - Israel Institute of Technology (IIT)

  510. IMAGINi005-A (IMAGINE005)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal

  511. IMAGINi020-A (IMAGINE020)

    France Imagine Institute / INSERM U1163 (IMAGIN)

  512. IMAGINi021-A (IMAGINE021)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal

  513. IMAGINi022-A (IMAGINE022)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Waardenburg syndrome

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  521. IMBAi004-A (SCCF-733J clone#1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  522. IMBAi004-B (SCCF-733J clone#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  523. IMBAi004-C (SCCF-733J clone#17)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  524. IMBAi005-A (SCCF-734J clone#2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  525. IMBAi005-B (SCCF-734J clone#3)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  526. IMBAi005-C (SCCF-734J clone#10)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  527. IMBAi006-A (SCCF-735J clone#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  528. IMBAi006-B (SCCF-735J clone#17)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  529. IMBAi006-C (SCCF-735J clone#20)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

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

    Wolfram syndrome 1

  531. IMGTi001-B (iTAF5-32)

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

    Monosomy 22q13.3

  532. IMGTi003-A (iTAF6-6)

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

    Ring chromosome 13 syndrome

  533. INSRMi002-A (PC117_c2)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  534. INSRMi004-A (PC118_c7)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  535. INSRMi006-A (PC131_c8)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  536. INSRMe002-A (STR-I-233-FRAXA)

    France INSERM (INSRM)
    Disease:

    Fragile x syndrome

  537. INSRMe005-A (STR-I-189-FRAXA)

    France INSERM (INSRM)
    Disease:

    Fragile x syndrome

  538. INSRMe011-A (STR-I-229-MTMX)

    France INSERM (INSRM)
    Disease:

    X-linked myopathy with excessive autophagy

  539. INSRMe012-A (STR-I-231-MTMX)

    France INSERM (INSRM)
    Disease:

    X-linked myopathy with excessive autophagy

  540. INSRMe016-A (STR-I-347-FRAXA)

    France INSERM (INSRM)
    Disease:

    Fragile x syndrome

  541. IPTi001-A (15M0008)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  542. IPTi002-A (15F0009)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  543. IPTi003-A (15M0010)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  544. IPTi004-A (15M0011)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Obsolete_alzheimer's disease

  545. IPTi005-A (16M0064)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal

  546. IPTi006-A (16M0065)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal

  547. IPTi007-A (16F0066)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal

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

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

    Normal

  549. IRMBi001-A (AD-PS1 hiPSC)

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

    Obsolete_alzheimer's disease

  550. IRMBi002-A (AD-APP hiPSC)

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

    Obsolete_alzheimer's disease

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

  555. ISCRMi001-A (3-0062 and DSP Leu462fs)

    United States University of Washington Institute for Stem Cell and Regenerative Medicine (ISCRM)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

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

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

    Marfan syndrome

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

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

    Marfan syndrome

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

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

    Marfan syndrome

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

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

    Marfan syndrome

  560. ISMMSi044-A (PLNR14del-1BC1)

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

    Cardiomyopathy

  561. ISMMSi045-A (PLNR14del-2BC4)

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

    Cardiomyopathy

  562. ISMMSi047-A (PLN-R14del-4AC4)

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

    Cardiomyopathy

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

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

    Cardiomyopathy

  564. ISMMSi049-A (PLN-1CC1)

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

    Normal

  565. ISMMSi050-A (PLN-4CC4)

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

    Normal

  566. ISMMSi051-A (PLN-5AC2)

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

    Normal

  567. ISTEMi001-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease type iii

  568. ISTEMi002-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease type iii

  569. ISTEMi003-A

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Glycogen storage disease type iii

  570. CEBe033-A-8 (SA001_KO_HGPRT_1)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Lesch-nyhan syndrome

  571. CEBe033-A-9 (SA001_KO_HGPRT_2)

    France Institut from Stem cell Therapy and Exploration of Monogenic diseases (ISTEM)
    Disease:

    Lesch-nyhan syndrome

  572. ITXi012-A (Lp(a) Cl23)

    France l’institut du thorax (ITX)
    Disease:

    Hyperlipoproteinemia

  573. JTUi001-A

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

    Charge syndrome

  574. JTUi002-A

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

    Waardenburg syndrome

  575. JTUi007-A

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

    Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

  576. JUCGRMi001-A (VPS35A4)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson's disease

  577. JUCGRMi001-B (VPS35A5)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson's disease

  578. JUCGRMi001-C (VPS35A8)

    Japan Center for Genomic and Regenerative Medicine, Juntendo University (JUCGRM)
    Disease:

    Parkinson's disease

  579. JUFMDOi007-A

    Japan Juntendo University Faculty of Medicine, Department of Otorhinolaryngology (JUFMDO)
    Disease:

    Ush2a

  580. WAe001-A-1S (MB-/-#1)

    Saudi Arabia King Abdullah International Medical Research Center (KAIMRC)
    Disease:

    Normal

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Klinefelter's syndrome

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

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

    Developmental and epileptic encephalopathy

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

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

    Developmental and epileptic encephalopathy

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

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

    Normal

  607. KGUi001-A (AR1023)

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

    Obsolete_bipolar disorder

  608. KGUi002-A (AR1034)

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

    Obsolete_bipolar disorder

  609. KLRMMEi001-A

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

    Retinitis pigmentosa

  610. KLRMMEi003-A

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

    Usher syndrome

  611. KMUGMCi003-A (KMUGMCi003ERCC2 and KN610)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Trichothiodystrophy 1, photosensitive

  612. KMUGMCi005-A (KMUGMCi005TMC8 and KN627)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Epidermodysplasia verruciformis

  613. KMUGMCi006-A (TS271 #12 WT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  614. KMUGMCi006-B (TS271 #5 MT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  615. KMUGMCi006-C (TS271 #21 WT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  616. KMUGMCi006-D (TS271 #23 WT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  617. KMUGMCi006-E (TS271 #4 MT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  618. KMUGMCi006-F (TS271 #20 MT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  619. KMUGMCi007-A (KMUGMCi007PEPD and KN649)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Prolidase deficiency

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

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

    Normal

  621. KSCBi005-A (CMC-hiPSC-003)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal

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

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Osteogenesis imperfecta type 1

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

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Prader-willi syndrome

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

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Senior-loken syndrome

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

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Leber congenital amaurosis

  626. KSCBi017-A (PB01-EiPS21)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal

  627. BIONi010-C-56 (BIONi010-C-A713T-C25)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  628. BIONi010-C-57 (BIONi010-C-A713T-C42)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  629. BIONi010-C-58 (BIONi010-C-A713T-C1)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  630. BIONi010-C-59 (BIONi010-C-A713T-C33)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  631. BIONi010-C-60 (BIONi010-C-R589C-C7)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  632. BIONi010-C-61 (BIONi010-C-R589C-C16)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  633. BIONi010-C-62 (BIONi010-C-R589C-C5)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  634. BIONi010-C-63 (BIONi010-C-R589C-C9)

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  635. KUIFMSi004-A (201B1)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  636. KUIFMSi004-B (201B6)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  637. KUIFMSi004-C (201B7)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  638. KUIFMSi004-D (201B2)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  639. KUIFMSi004-E (201B3)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  640. KUIFMSi009-A (243H1)

    Japan Kyoto University (KUIMS)

  641. KUIFMSi009-B (243H7)

    Japan Kyoto University (KUIMS)

  642. KUIFMSi011-A (246G1)

    Japan Kyoto University (KUIMS)

  643. KUIFMSi011-B (246G3)

    Japan Kyoto University (KUIMS)

  644. KUIFMSi011-C (246G4)

    Japan Kyoto University (KUIMS)

  645. KUIFMSi011-D (246G5)

    Japan Kyoto University (KUIMS)

  646. KUIFMSi011-E (246G6)

    Japan Kyoto University (KUIMS)

  647. KUMi001-A (KUMi001-A_CML(Ph+))

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

    Philadelphia-positive myelogenous leukemia

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

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

    Chronic myeloid leukemia

  649. KUMi003-A

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

    Acute promyelocytic leukemia

  650. KUMi004-A

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

    Chronic lymphocytic leukemia

  651. KUMi005-A

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

    Multiple myeloma

  652. KUMi006-A

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

    Multiple myeloma

  653. KUMCi001-A (ALLCD34+)

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

    Acute lymphoblastic leukemia

  654. KUMCi002-A (MM_CD34+iPSCs)

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

    Multiple myeloma

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

    South Korea Konkuk University (KUSCRB)
    Disease:

    Age-related macular degeneration

  656. LCPHi001-A

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

    Obsolete_parkinson's disease

  657. LCPHi002-A

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

    Parkinson's disease

  658. LCPHi003-A

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

    Parkinson's disease

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

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

    Parkinson's disease

  660. 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

  661. 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

  662. LCSBi011-A (RHOT1_T351A_clone1_PD)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson's disease

  663. LCSBi012-A (RHOT1_T610A_clone6_PD)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson's disease

  664. LEIi006-A

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  665. UCSFi001-A-72 (FUS-R521G HET 2B10 and LSUHSi004-A-72)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  666. UCSFi001-A-73 (FUS-R521G HOM 1D9)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  667. UCSFi001-A-74 (FUS-P525L HET 2D1)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  668. UCSFi001-A-75 (FUS-P525L HOM 2D2)

    United States LSU Health Sciences Center in Shreveport (LSUHS)
    Disease:

    Amyotrophic lateral sclerosis

  669. LUBi001-A (PGRN-8310, PGRN8310, RCi195 and RCFB58 c12.5)

    Denmark H. Lundbeck A/S (LUB)
    Disease:

    Frontotemporal dementia

  670. LUBi001-B (PGRN-8310, RCFB58 c4.4, PGRN8310 and RCi194)

    Denmark H. Lundbeck A/S (LUB)
    Disease:

    Frontotemporal dementia

  671. LUBi001-C (PGRN-8310, RCFB58 c3.7, RCi200 and PGRN8310)

    Denmark H. Lundbeck A/S (LUB)
    Disease:

    Frontotemporal dementia

  672. CRMi003-A-2

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  673. CRMi003-A-3 (Proliving and GMNN-mScarletI Reporter)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  674. LUMCi004-A-1 (LU99_AAVS1-bxb-v2)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  675. LUMCi004-A-2 (LU99_CLYBL-bxb-v2)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  676. LUMCi013-A (LUMC0133iCTRL06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  677. LUMCi014-A (LUMC0134iCTRL29)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  678. LUMCi015-A (LUMC0135iCTRL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  679. LUMCi016-A (LUMC0136iCTRL09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  680. LUMCi027-A (LUMC0153iPKP03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Arrhythmogenic right ventricular dysplasia 9

  681. LUMCi027-A-1 (iso01LUMC0153iPKP03 and LUMC0153iPKP03corr#22)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Arrhythmogenic right ventricular dysplasia 9

  682. LUMCi028-A (LUMC0020iCTRL06 and FLB6)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  683. LUMCi045-A (LUMC0145iKLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  684. LUMCi045-A-1 (iso01LUMC0145iKLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  685. LUMCi046-A (LUMC0146iKLHL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  686. LUMCi046-A-1 (iso2LUMC0146iKLHL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  687. LVPEIi001-A (hiPSC-F2-3F1)

    India L.V. Prasad Eye Institute (LVPEI)
    Disease:

    Normal

  688. LZUSHi002-A

    China Lanzhou University Second Hospital (LZUSH)
    Disease:

    Madd

  689. MCRIi004-A (PB004)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal

  690. MCRIi005-A (PB005)

    Australia Murdoch Children's Research Institute (MCRI)
    Disease:

    Normal

  691. MDCi007-A (8993-A12)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  692. MDCi008-A (8993-B12)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  693. MDCi009-A (8993-C11)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  694. MDCi010-A (8993-D7)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  695. MDCi011-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal

  696. MDCi011-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal

  697. MDCi012-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal

  698. MDCi012-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal

  699. MDCi013-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal

  700. MDCi013-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal

  701. MDCi014-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal

  702. MDCi014-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal

  703. MHRCCGi001-A (P1SH)

    Russia Laboratory Clinical Genetics (MHRCCG)
    Disease:

    Schizophrenia

  704. MHRCCGi004-A (A1SH)

    Russia Laboratory Clinical Genetics (MHRCCG)
    Disease:

    Normal

  705. MHRCCGi005-A (A2SH)

    Russia Laboratory Clinical Genetics (MHRCCG)
    Disease:

    Normal

  706. MILi001-A (K10 and hFF-iPSCs)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal

  707. MILi001-B (F5)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal

  708. MILi001-C (F10)

    Germany Miltenyi Biotec B.V. & Co. KG (MIL)
    Disease:

    Normal

  709. MMCi002-A (MMC-iPSC-002-A)

    Taiwan Mackay Medical College (MMC)
    Disease:

    Hearing loss

  710. MUi028-A

    Thailand Mahi