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  1. AAKIPSi001-A

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

    Aniridia

  2. AAKIPSi002-A

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

    Aniridia

  3. AAKIPSi003-A

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

    Aniridia

  4. ABi001-A

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

    Cone dystrophy with supernormal rod response

  5. ABi002-A

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

    Cone dystrophy with supernormal rod response

  6. AHQUi001-A (IPS35-2)

    China Affiliated Hospital of Qingdao University (AHQU)
    Disease:

    Non rare in europe: hyperlipoproteinemia type 4

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

    China Affiliated Hospital of Qingdao University (AHQU)
    Disease:

    Non rare in europe: hyperlipoproteinemia type 4

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

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

    Normal

  9. WAe009-A-79

    China Anzhen Hospital (ANZHEN)
    Disease:

    Long qt syndrome 1

  10. HVRDe009-A-2 (HUES9 CTNNB1 3X FLAG)

    United States Arizona State University (ASU)
    Disease:

    Normal

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

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

    Normal

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

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

    Normal

  13. BBANTWi001-C (iPSC_FB_M45-50_C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Normal

  14. BBANTWi006-A (iPSC_BrS9_FB_C7)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome 1

  15. BBANTWi007-A (iPSC_BrS10_FB_C3)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Brugada syndrome 1

  16. BBANTWi008-A (iPSC_PBMC_LDS_SMAD3_T1_C11)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 3

  17. BBANTWi010-A (iPSC_PBMC_LDS_TGFB3_KE2M_C9)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 5

  18. BBANTWi011-A

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Familial thoracic aortic aneurysm and aortic dissection

  19. BCHNi001-A (BCHi001-A)

    China Beijing Childrenâ€Čs HospitalDepartment of Nephrology (BCHN)
    Disease:

    Bardet-biedl syndrome

  20. BCHNCi001-A

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

    Early infantile epileptic encephalopathy

  21. BGUi008-A (DCM-C)

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

    Left ventricular noncompaction cardiomyopathy

  22. BIHi002-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Autosomal recessive osteopetrosis 4

  23. BIHi030-C

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  24. BIOi002-A

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Autosomal dominant optic atrophy

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

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Hereditary retinal dystrophy

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Frontotemporal dementia

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Huntington disease

  30. STBCi006-A-1 (ApoE KO)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Mody

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Inflammatory disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

  59. BIONi010-C-51

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Hungary BioTalentum Ltd. (BIOT)
    Disease:

    Obsolete_alzheimer's disease

  72. BJTTHi001-A

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Normal

  73. BRCi021-A (TUH1)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Cardiomyopathy

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BSC)
    Disease:

    Alzheimer disease

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

    United States Boston University (BUCREM)
    Disease:

    Lethal brain and heart developmental defects

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

    United States Boston University (BUCREM)
    Disease:

    Lethal brain and heart developmental defects

  79. CAMi002-C (FiPS 2c)

    United Kingdom University of Cambridge (CAM)
    Disease:

    Normal

  80. CBCHi001-A-1

    China Beijing Chest Hospital (CBCH)
    Disease:

    Hypertrophic cardiomyopathy

  81. CBIGi001-A (AIW002-02)

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

    Normal

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

  86. CDIi001-A (01279)

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

    Normal

  87. CDIi002-A (01434)

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

    Normal

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

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

    Normal

  89. CENSOi002-B (FB74R2c4 and CENSOi261)

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

    Duchenne muscular dystrophy

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

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

    Transient abnormal myelopoiesis associated with down syndrome

  121. CHULAe001-A (Chula2.hES)

    Thailand Chulalongkorn University (CHULA)
  122. CIAUi002-C (UBC3 M1)

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

    Left bundle branch block

    Disease:

    Nonischemic cardiomyopathy

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

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

    Catecholaminergic polymorphic ventricular tachycardia 2

  124. CIAUi003-A-1 (BFC4-C and BFC4-CRISPR-corrected)

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

    Catecholaminergic polymorphic ventricular tachycardia 2

  125. CIMRi001-A (GM27291)

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

    Vici syndrome

  126. CIPi001-A

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

    Benign familial infantile epilepsy

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

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

    Facioscapulohumeral muscular dystrophy 2

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

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

    Facioscapulohumeral muscular dystrophy 2

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

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

    Facioscapulohumeral muscular dystrophy 2

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

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

  131. CMCi007-A (CMC-Fb-004)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

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

    South Korea Catholic University of Korea (CMC)
    Disease:

    Birt-hogg-dube syndrome

  133. CMCi010-A (CMC-Fb-002)

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

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

    South Korea Catholic University of Korea (CMC)
    Disease:

    Dent disease

  135. CMFTe002-A (Man-12)

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

    Normal

  136. CMFTe003-A (Man-14)

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

    Normal

  137. CMFTe004-A (Man-16)

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

    Normal

  138. CMGANTi003-A (SEMD1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  139. CMGANTi004-A (SEMD2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  140. CMGANTi006-A (SEDC1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Spondyloepiphyseal dysplasia congenita

  141. CPGHi004-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal

  142. CPGHi006-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Autosomal dominant polycystic kidney disease

  143. CPGHi007-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal

  144. CPGHi008-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Autosomal recessive polycystic kidney disease

  145. CRTDi011-C (IDP52555 #36)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  146. CSSi009-A (GDB1307_Z2#1)

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

    Gnb5-related intellectual disability-cardiac arrhythmia syndrome

  147. CSUXHi003-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Waardenburg syndrome type 2

  148. CSUXHi004-A

    China Xiangya Hospital (CSUXH)
    Disease:

    Waardenburg syndrome type 1

  149. CUBi001-A

    Germany Charité - UniversitÀtsmedizin Berlin (CUB)
    Disease:

    Mirage syndrome

  150. CUBi002-B

    Germany Charité - UniversitÀtsmedizin Berlin (CUB)
    Disease:

    Mirage syndrome

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

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

    Normal

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

  162. DHMi001-A (Control_S)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal

  163. DHMi002-A (HLHS_606)

    Germany German Heart Center Munich (DHM)
    Disease:

    Hypoplastic left heart syndrome

  164. DHMi003-A (HLHS_612)

    Germany German Heart Center Munich (DHM)
    Disease:

    Hypoplastic left heart syndrome

  165. DHMi004-A (HOS_1460)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  166. DHMi004-A-1 (HOS_1460corr 127 Clone 31)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  167. DHMi004-A-2 (HOS_1460_FLAG Clone 4)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  168. DHMi004-A-3 (HOS_1460corr 127 Clone 31_FLAG Clone 18)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  169. DHMi005-A (Control_L)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal

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

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal

  171. DHMi005-A-3 (L_FLAG Clone 6)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal

  172. DHMi005-A-4 (L_FLAG Clone 7)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal

  173. DHMi005-A-5 (L_mut_FLAG Clone 4)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  174. DHMi005-A-6 (L_mut_FLAG Clone 14)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  175. DHMi005-A-7 (L_mut_FLAG Clone 15)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  176. DRICUi006-A (ADANG10496CA)

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

    Late-onset alzheimers disease

  177. DRICUi007-A (ADANG10605CA)

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

    Late-onset alzheimers disease

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

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

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

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  180. EDi011-C (RCi141)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  181. EDi012-C (RCi165)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  182. EDi013-C (RCi214)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  183. EDi015-C (RCi184)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Unipolar depression

  184. EDi016-C (RCi191)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  185. EDi017-C (RCi182)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  186. EDi018-C (RCi213)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  187. EDi019-C (RCi168)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

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

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

    Normal

  189. EHTJUi003-A (DF-GMP-ZB12AD-H)

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

    Normal

  190. EHTJUi004-A (DF-GMP-ZB12AN-I)

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

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    X-linked creatine transporter deficiency

  192. ESi004-A ([GD]FiPS-4F-21c)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Gaucher disease

  193. ESi006-A (SP13#4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  194. ESi008-B (KiPS3F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  195. ESi031-A (XFiPS-F44-3F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  196. ESi031-B (FiPS-3F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  197. ESi031-C (FiPS-4F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  198. ESi031-D (FiPS-4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  199. ESi038-A (CBiPS32-2F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  200. ESi038-C (CBiPS32-3F-12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Retinitis pigmentosa

  207. ESi078-A (cPRPF31-MiPS4F7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  208. ESi082-A (CRB1-MiPS4F1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Macular degeneration

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  216. ESe010-A (ES-3)

    Spain Spanish Stem Cell Bank (ES)
  217. ESe013-A (VAL-5)

    Spain Spanish Stem Cell Bank (ES)
  218. ESe021-A (VAL-8)

    Spain Spanish Stem Cell Bank (ES)
  219. ESe027-A (pES12)

    Spain Spanish Stem Cell Bank (ES)
  220. ESe029-A (AND-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  221. FAMRCi001-A (ARVC2)

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

    Arrhythmogenic right ventricular cardiomyopathy

  222. FAMRCi001-B (ARVC4)

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

    Arrhythmogenic right ventricular cardiomyopathy

  223. FAMRCi002-A (OBC7)

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

    Desminopathy

  224. 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

  225. 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

  226. FAMRCi009-A (RCMP43)

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

    Restrictive cardiomyopathy

  227. FDCHi004-A (iPS-39)

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

    Osteogenesis imperfecta

  228. FDCHi010-A (iPSCx-y-AHDC1-m)

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

    Xia-gibbs syndrome

  229. FDHPIi001-A

    China (WITHDRAWN) Fudan University (FDHPI)
    Disease:

    Neurodegeneration

  230. 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

  231. FJMUUHi001-A

    China Fujian Medical University Union Hospital (FJMUUH)
    Disease:

    Parkinson's disease 7

  232. 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

  233. GIBHi003-A (PINK1-I368N-C2)

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

    Parkinson's disease

  234. GWCMCi001-A (iPS-57)

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

    Iga glomerulonephritis

  235. HADe004-A (HAD 4)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Familial dysautonomia

  236. HADe007-A (HAD-C 100)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  237. HADe007-B (HAD-C 100 Single Cell, Feeder-Free Bank (Seed Cell Bank, SCB))

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  238. HADe007-C

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  239. HADe008-A (HAD-C 102)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  240. HADe008-B (HAD-C 102 Single cell, Feeder-free (Seed Cell Bank, SCB))

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  241. HADe009-A (HAD-C 106)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

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

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  243. HADe010-A (HAD-C 103 cGMP-grade, xeno-free, Single-cell, Feeder-free Master-Cell Bank)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

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

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

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

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

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

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal

  247. HHUi003-B (A4_C1)

    Germany UniversitĂ€tsklinikum DĂŒsseldorf (HHU)
    Disease:

    Maternally-inherited leigh syndrome

  248. HHUi003-C (A4_W1)

    Germany UniversitĂ€tsklinikum DĂŒsseldorf (HHU)
    Disease:

    Maternally-inherited leigh syndrome

  249. HHUi006-A (11656_H)

    Germany UniversitĂ€tsklinikum DĂŒsseldorf (HHU)
    Disease:

    Normal

  250. HHUi006-B (11656_K)

    Germany UniversitĂ€tsklinikum DĂŒsseldorf (HHU)
    Disease:

    Normal

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

    Germany Heinrich-Heine-UniversitĂ€t DĂŒsseldorf (HHUUKD)
    Disease:

    Normal

  252. HIHDNDi001-A (A30P-3, SNCA3 and Tue_020_A)

    Germany Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tuebingen (HIHDND)
    Disease:

    Autosomal dominant parkinson disease 1

  253. HIHDNDi001-B (A30P-4, SNCA4 and Tue_020_B)

    Germany Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tuebingen (HIHDND)
    Disease:

    Autosomal dominant parkinson disease 1

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

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

    Dilated cardiomyopathy

  255. HMGUi003-A

    Germany Helmholtz Zentrum MĂŒnchen (HMGU)
  256. HNMUi002-A (iPS-UC1291)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  257. HNMUi003-A (iPS-UC1290)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  258. HNMUi004-A (iPS-AF717)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  259. HNMUi005-A (iPS-UC1056)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  260. HNMUi006-A (iPS-UC1055)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  261. HNMUi007-A (iPS-AF0442)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  262. HNMUi008-A (iPS-UC2419)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  263. HNMUi009-A (iPS-UC1171)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  264. HNMUi010-A (iPS-AF091)

    China Hainan Medical University (HNMU)
    Disease:

    Thalassemia

  265. HVRDi004-B-1 (ENCBS369AAA and iNGN)

    United States Harvard University (HVRD)
    Disease:

    Normal

  266. HVRDe010-A (HuES10)

    United States Harvard University (HVRD)
  267. HVRDe011-A (HuES11)

    United States Harvard University (HVRD)
  268. HVRDe015-A (HuES15)

    United States Harvard University (HVRD)
  269. IAIi010-A (Kif5A 1847 C3)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Autosomal dominant spastic paraplegia type 10

  270. IBBISTi004-C (AS-GB clone 22)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

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

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

    Cystic fibrosis

  272. BIONi010-C-66 (BIONi010-C-N7)

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

    Cystic fibrosis

  273. ICANi001-A (CDGEN1.16)

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

    Hypertrophic cardiomyopathy

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

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

    Hypertrophic cardiomyopathy

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

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

    Normal

  276. ICANi002-A-2 (SCN5A-Clone 5)

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

    Normal

  277. ICGi002-C (DMD1_11)

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

    Duchenne muscular dystrophy

  278. ICGi018-C (iHD38Q-1)

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

    Huntington's disease

  279. ICGi020-A (ATP7bIL23f)

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

    Wilson disease

  280. ICGi020-B (ATP7bIL24f)

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

    Wilson disease

  281. 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

  282. 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

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

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

    Hypertrophic cardiomyopathy

  284. ICGi022-A-4 (K7-MYBPC3-N515del-2)

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

    Hypertrophic cardiomyopathy

  285. ICGi022-A-5 (K7-MYBPC3-N515del-3)

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

    Hypertrophic cardiomyopathy

  286. ICGi030-A (HF2)

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

    Wilson disease

  287. ICGi033-C (77Q-20)

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

    Huntington disease

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

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

    Obsolete_parkinson's disease

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

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

    Obsolete_parkinson's disease

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

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

    Obsolete_parkinson's disease

  291. ICGi036-A (FH 1.3.1S)

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

    Hyperlipoproteinemia, type iia

  292. ICGi037-A (FH 3.2.8T)

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

    Hyperlipoproteinemia, type iia

  293. ICGi038-A (FH 5.1.2Sh)

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

    Hyperlipoproteinemia, type iia

  294. ICGi039-C (PD31-15)

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

    Normal

  295. ICGi042-C (PD12-6Lm)

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

    Parkinson's disease

  296. ICGi043-A (LR-21)

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

    Parkinson's disease

  297. ICGi043-C (LR-15)

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

    Parkinson's disease

  298. ICGi044-A (PD40-7)

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

    Parkinson's disease

  299. ICGi044-B (PD40-8)

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

    Parkinson's disease

  300. ICGi044-C (PD40-13)

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

    Parkinson's disease

  301. HMGUi001-A-8 (C-PEP-mCherry-hiPSC)

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

    Normal

  302. IMAGINi002-A (IMAGINE002)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Epidermolysis bullosa

  303. IMAGINi003-A (IMAGINE003)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Epidermolysis bullosa

  304. IMAGINi020-A (IMAGINE020)

    France Imagine Institute / INSERM U1163 (IMAGIN)
  305. IMAGINi022-A (IMAGINE022)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Waardenburg syndrome

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  310. IMBAi007-C (SCCF-180J clone#21)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  311. IMBAi008-C (SCCF-181J clone#24)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  312. IMGTi001-A (iTAF5-29)

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

    Monosomy 22q13.3

  313. IMGTi001-B (iTAF5-32)

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

    Monosomy 22q13.3

  314. WAe009-A-76

    Austria IMP - Research Institute of Molecular Pathology (IMP)
    Disease:

    Normal

  315. INSRMi002-A (PC117_c2)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  316. INSRMi004-A (PC118_c7)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  317. INSRMi005-A (PC119_c7)

    France INSERM (INSRM)
    Disease:

    Normal

  318. INSRMi006-A (PC131_c8)

    France INSERM (INSRM)
    Disease:

    Epilepsy

  319. INSRMi007-A (pc132-c4)

    France INSERM (INSRM)
    Disease:

    Normal

  320. INSRMe001-A (OSCAR)

    France INSERM (INSRM)
    Disease:

    Normal

  321. 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

  322. ISFi001-A (HMGU1 and #1)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Normal

  323. ISMMSi017-C (MSN14-06S)

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

    Normal

  324. ISMMSi028-C (MSN25-09S)

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

    Normal

  325. ITXi001-A-1 (GPR146KO Cl2)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  326. JNCSRe001-A (BJNhem19)

    India Jawaharlal Nehru Centre for Advanced Scientific Research (JNCSR)
  327. JNCSRe002-A (BJNhem20)

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

    Normal

  328. JUCGRMi001-C (VPS35A8)

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

    Parkinson's disease

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

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

    Normal

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

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

    Normal

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

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

    Klinefelter's syndrome

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

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

    Developmental and epileptic encephalopathy

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

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

    Developmental and epileptic encephalopathy

  334. WAe001-A-C (H1X-10/H1.3-62)

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

    Normal

  335. KCLe015-A (KCL011)

    United Kingdom King's College London (KCL)
  336. KEIOi001-A (SM4-4-5)

    Japan Keio University (KEIO)
    Disease:

    Amyotrophic lateral sclerosis type 10

  337. KIe002-A (HS207)

    Sweden Karolinska Institutet (KI)
    Disease:

    Normal

  338. KIe024-A (HS429)

    Sweden Karolinska Institutet (KI)
  339. KIe024-A-1 (HS429A)

    Sweden Karolinska Institutet (KI)
  340. KIe024-A-2 (HS429B)

    Sweden Karolinska Institutet (KI)
  341. KIe024-A-3 (HS429C)

    Sweden Karolinska Institutet (KI)
  342. KIe024-A-4 (HS429D)

    Sweden Karolinska Institutet (KI)
  343. KIe026-A (HS480)

    Sweden Karolinska Institutet (KI)
  344. KLRMMEi001-A

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

    Retinitis pigmentosa

  345. KLRMMEi003-A

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

    Usher syndrome

  346. KMUGMCi006-C (TS271 #21 WT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

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

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal

  348. KSCBi005-A-1 (CMC-hiPSC-003(Nestin-GFP) and CMC-003i-Nestin.EGFP)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal

  349. KSCBi005-A-2 (CMC-hiPSC-003(Sox1-GFP) and CMC-003i-Sox1.EGFP)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal

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

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal

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

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Osteogenesis imperfecta type 1

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

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Senior-loken syndrome

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

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Leber congenital amaurosis

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

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

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

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

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

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

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

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

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

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

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

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

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

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

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

    Denmark University of Copenhagen (KU)
    Disease:

    Epilepsy

  362. KUe008-A (LRB08)

    Denmark University of Copenhagen (KU)
  363. KUe012-A (LRB014)

    Denmark University of Copenhagen (KU)
  364. KUe013-A (LRB016)

    Denmark University of Copenhagen (KU)
  365. KUIFMSi004-B (201B6)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  366. KUIFMSi004-C (201B7)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  367. KUIFMSi004-D (201B2)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  368. KUIFMSi004-E (201B3)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  369. KUIFMSi011-C (246G4)

    Japan Kyoto University (KUIMS)
  370. LCPHi001-A

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

    Obsolete_parkinson's disease

  371. LCPHi002-A

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

    Parkinson's disease

  372. LCPHi003-A

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

    Parkinson's disease

  373. LCSBi002-B (ND40066-clone 7 and ND40066-PINK1/PARK6-ILE368ASN-clone 7)

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

    Parkinson's disease

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

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

    Parkinson's disease

  375. LEIi004-A-1

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

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

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

    Amyotrophic lateral sclerosis

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

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

    Amyotrophic lateral sclerosis

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

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

    Amyotrophic lateral sclerosis

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

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

    Amyotrophic lateral sclerosis

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

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

    Frontotemporal dementia

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

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

    Frontotemporal dementia

  382. LUMCi002-C (113-8 and LUMC0113iATAX08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  383. LUMCi003-A (114-1 and LUMC0114iCTRL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  384. LUMCi003-B (114-2 and LUMC0114iCTRL02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  385. LUMCi004-C (LUMC0031iCTRL08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  386. LUMCi008-C (152-4 and LUMC0152iHD04)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

  387. LUMCi022-C (115-7 and LUMC0115iATAX07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  388. LUMCi027-A (LUMC0153iPKP03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Arrhythmogenic right ventricular dysplasia 9

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

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Arrhythmogenic right ventricular dysplasia 9

  390. LUMCi039-A (LQT1-1781G/A hiPSC and LUMC0021iKCNQ-30)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Long qt syndrome 1

  391. LUMCi045-A-1 (iso01LUMC0145iKLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  392. LUMCi046-A-1 (iso2LUMC0146iKLHL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  393. MCRIi001-A (PB001)

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

    Normal

  394. MCRIi001-A-1 (PB001-OI26)

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

    Osteogenesis imperfecta

  395. MDCi008-A (8993-B12)

    Germany Max DelbrĂŒck Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  396. MDCi233-A

    Germany Max DelbrĂŒck Center Berlin Buch (MDC)
    Disease:

    Limb-girdle muscular dystrophy type 2b

  397. MDCi233-B

    Germany Max DelbrĂŒck Center Berlin Buch (MDC)
    Disease:

    Limb-girdle muscular dystrophy type 2b

  398. MICCNi001-A (ADHD Stem Cell Study_subject 6, hiPSC_03 family control sibling and clone C1)

    Australia ​Monash Institute of Cognitive and Clinical Neurosciences (MICCN)
    Disease:

    Normal

  399. MICCNi001-B (ADHD Stem Cell Study_subject 6, hiPSC_03 family control sibling and clone C2)

    Australia ​Monash Institute of Cognitive and Clinical Neurosciences (MICCN)
    Disease:

    Normal

  400. MICCNi002-A (ADHD Stem Cell Study_subject 5, clone A1 and hiPSC_03 affected sibling)

    Australia ​Monash Institute of Cognitive and Clinical Neurosciences (MICCN)
    Disease:

    Attention deficit hyperactivity disorder

  401. MICCNi002-B (ADHD Stem Cell Study_subject 5, hiPSC_03 affected sibling and clone A16)

    Australia ​Monash Institute of Cognitive and Clinical Neurosciences (MICCN)
    Disease:

    Attention deficit hyperactivity disorder

  402. MILi001-C (F10)

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

    Normal

  403. MLUi007-J

    Germany Medical Faculty of the Martin Luther University Halle-Wittenberg (MLU)
    Disease:

    Alzheimer disease

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

    Taiwan Mackay Medical College (MMC)
    Disease:

    Hearing loss

  405. MRIi001-A (C6)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal

  406. MRIi003-A (HK)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal

  407. MRIi018-A (HLHS_375)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Hypoplastic left heart syndrome

  408. MUNIi002-A (MDMD02)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  409. MUNIi005-A (fAD1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer disease 3

  410. MUNIi006-A (fAD2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer disease 3

  411. MUNIi007-A (fAD3 and ADF81)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer disease 4

  412. MUNIi018-C (HUVEC-hiPSC-macroH2A1.2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal

  413. MUSIi005-A (SUiPSC02)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal

  414. MUSIi006-A (SKiPSC02)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal

  415. MUSIi011-A (STiPSC01.1)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal

  416. MUSIi011-B (STiPSC01.8)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal

  417. MUSIi019-A (SLC4A1-21-C1)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Distal renal tubular acidosis

  418. NCHi001-A (LCL-iPSC4802)

    United States Nationwide Children's Hospital (NCH)
    Disease:

    Congenital heart disease

  419. NERCi001-A

    China National Engineering and Research Center of Human Stem Cell (NERC)
    Disease:

    Dyskeratosis congenita

  420. TMOi001-A-5 (DISC1 Ex2 D5)

    Germany NMI Natural and Medical Sciences Institute at the University of TĂŒbingen (NMI)
    Disease:

    Normal

  421. TMOi001-A-6 (DISC1 Ex2 C4)

    Germany NMI Natural and Medical Sciences Institute at the University of TĂŒbingen (NMI)
    Disease:

    Normal

  422. NMIi011-C (B1.7)

    Germany NMI Natural and Medical Sciences Institute at the University of TĂŒbingen (NMI)
    Disease:

    Breast carcinoma

  423. NTUHi002-A

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Aceruloplasminemia

  424. NUIGi003-A (LQT002C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  425. NUIGi003-B (LQT002C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  426. NUIGi004-A (LQT003C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  427. NUIGi005-A (LQTS004C7 and LQT004C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  428. NUIGi005-B (LQTS004C9 and LQT004C9)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  429. NUIGi005-C (LQTS004Cx and LQT004Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  430. NUIGi006-A (LQTS005C2 and LQT005C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  431. NUIGi006-B (LQTS005C4 and LQT005C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  432. NUIGi006-C (LQTS005Cx and LQT005Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  433. NUIGi007-A (LQTS006C6 and LQT006C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  434. NUIGi007-B (LQTS006C8 and LQT006C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  435. NUIGi008-A (LQTS007C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  436. NUIGi008-B (LQTS007C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  437. NUIGi008-C (LQTS007Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  438. NUIGi009-A (LQTS008C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  439. NUIGi009-B (LQTS008C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  440. NUIGi009-C (LQTS008Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  441. NUIGi010-A (LQTS009C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  442. NUIGi010-B (LQTS009C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  443. NUIGi010-C (LQTS009Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  444. NUIGi011-A (LQTS010C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  445. NUIGi011-B (LQTS010C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  446. NUIGi011-C (LQTS010Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  447. NUIGi012-A (LQT011C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  448. NUIGi015-A (LQT014C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  449. NUIGi015-B (LQT014C9)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  450. NUIGi015-C (LQT014C12)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  451. NUIGi018-C (LQT017Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal

  452. NUIGi020-A (LQT019C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  453. NUIGi020-B (LQT019C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  454. NUIGi020-C (LQT019Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  455. NUIGi038-B-1 (CR.LQTH002Cx-A17)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  456. NUIGi038-B-2 (CR.LQTH002Cx-A21)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  457. NUIGi038-B-3 (CR.LQTH002Cx-3A15)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  458. NUIGi038-B-4 (CR.LQTH002Cx-3A18)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  459. NUIGi038-C (LQTH002C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal

  460. NUIGi043-C (ALS52C10)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  461. NUIGi044-C (ALS69C6)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  462. NUIGi046-C (LQTH001C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal

  463. NUIGi047-C (LQTH003Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal

  464. NUIGi048-C (ALSH84C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  465. NUIGi049-C (ALSH47C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  466. NUIGi050-C (ALS53C7)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  467. NUIGi051-C (ALS57C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  468. NUIGi052-A

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Non-specific early-onset epileptic encephalopathy

  469. NUIGi052-B

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Non-specific early-onset epileptic encephalopathy

  470. NUIGi052-C

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Non-specific early-onset epileptic encephalopathy

  471. NUIGi055-C (iPSC C1-17)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal

  472. NUIGi063-C (EP2003 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Kcnq2-related epileptic encephalopathy

  473. NUIGi064-C (EP2C003 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal

  474. NYSCFi001-C (AL0002-01-SV-008)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal

  475. NYSCFe003-A (NY0003-01-ES-001)

    United States New York Stem Cell Foundation Research Institute (NYSCF)
    Disease:

    Normal

  476. ORIONi001-A (iALS-1)

    Slovakia Biomedical center Martin, Jessenius Faculty of Medicine in Martin, COMENIUS UNIVERSITY IN BRATISLAVA (ORION)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  477. ORIONi002-A (iALS-2)

    Slovakia Biomedical center Martin, Jessenius Faculty of Medicine in Martin, COMENIUS UNIVERSITY IN BRATISLAVA (ORION)
    Disease:

    Sporadic amyotrophic lateral sclerosis

  478. RCi002-A (FP5C-14 and RCi92)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  479. PFIZi009-A (RCi188)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  480. PFIZi010-C (FB65c20)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome

  481. PFIZi013-A (RCi215 and RCFB59 C9)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Amyotrophic lateral sclerosis

  482. PFIZi014-A (OD002-s7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  483. PFIZi015-A (OD003-s5)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  484. PFIZi017-A (BC142c7 and RCi209)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  485. PFIZi018-A (BC143c8 and RCi207)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  486. PFIZi021-A (OD001-s7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  487. PFIZi022-A (B219c2)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epileptic encephalopathy

  488. PFIZi023-A (B217c8)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Bilateral frontoparietal polymicrogyria

  489. PFIZi024-A (B218c6)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epilepsy

  490. PFIZi025-A (B220c16)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epilepsy

  491. PFIZi028-A (B212c7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Neurodevelopmental disorder

  492. PFIZi029-A (B222c4)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Myoclonic epilepsy

  493. PFIZi030-A (B216c13)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Acromesomelic dysplasia

  494. PFIZi031-A (B213c1)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epileptic encephalopathy

  495. PHAi003-A (PIDi003-A)

    Sweden Pan-Hammarström laboratory (PHA)
    Disease:

    Primary immunodeficiency

  496. PHAi003-B (PIDi003-B)

    Sweden Pan-Hammarström laboratory (PHA)
    Disease:

    Primary immunodeficiency

  497. PMUi001-C (Chantal and BMACA-CT2-C)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal

  498. PMUi002-A (Cornelius and UCB144-CT2-C)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Normal

  499. PMUi002-A-1 (UCB144-CT2-C DOCK2KO clone 19 and Cornelius DOCK2KO clone 19)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Severe combined immunodeficiency

  500. PMUi002-A-2 (UCB144-CT2-C DOCK2KO clone 20 and Cornelius DOCK2KO clone 20)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Severe combined immunodeficiency

  501. PMUi002-A-3 (Cornelius DOCK2KO clone 22 and UCB144-CT2-C DOCK2KO clone 22)

    Austria Paracelsus Medical University (PMU)
    Disease:

    Severe combined immunodeficiency

  502. PNUSCRi001-A (GBA PD iPSC7)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Parkinson's disease

  503. PNUSCRi003-A (GBA Gaucher iPSC1)

    South Korea Pusan National University: Convergence Stem Cell Research Center (PNUSCR)
    Disease:

    Gaucher disease

  504. PUFHi004-A (TMEM163 c.227T>C p.(Leu76Pro) iPSC)

    China Peking University First Hospital (PUFH)
    Disease:

    Leukodystrophy

  505. WAe009-A-47

    China Peking University Third Hospital Department of Cardiology (PUHT)
    Disease:

    Cytochrome-c oxidase deficiency disease

  506. PUMCi002-A (AF-iPSCs and C1)

    China Peking Union Medical College (PUMC)
    Disease:

    Normal

  507. PUMCHi001-A (IPS-34)

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Familial partial lipodystrophy type 2

  508. PUMCHi001-A-1 (IPS34-R-17)

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Familial partial lipodystrophy type 2

  509. PUMCHi004-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Transthyretin amyloidosis

  510. PUMCHi005-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Transthyretin cardiac amyloidosis

  511. QBRIi001-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal

  512. QBRIi002-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal

  513. QBRIi005-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  514. QBRIi006-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  515. RAUi001-C

    Armenia Russian-Armenian University (RAU)
    Disease:

    Normal

  516. RCi004-A (PDSC-10 and RCi150)

    United Kingdom Roslin Cells (RC)
    Disease:

    Huntington disease

  517. RCi004-B (RCi68 and PDSC-3)

    United Kingdom Roslin Cells (RC)
    Disease:

    Huntington disease

  518. RCi005-A (FB71c4 and RCi171)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  519. RCi006-A (FB69c4 and RCi169)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  520. RCi007-A (FB70c1 and RCi170)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  521. RCi007-C

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  522. RCi009-A (Rci201 and FB73c6)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  523. RCMGi012-A (P11L3)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Maroteaux-lamy syndrome

  524. REGUi009-A (myasthenic syndrome due to mutation in ColQ and hiPS 5-9016)

    France Institute for Regenerative Medecine & Biotherapy U1183 (REGU)
    Disease:

    Congenital myasthenic syndrome

  525. SBWCHi001-A

    China Shenzhen Baoan Women's and Children's Hospital, Jinan University (SBWCH)
    Disease:

    Ctnnb1 gene mutation

  526. SCHi001-A-1 (AMN5-Corrected iPSC)

    South Korea Severance Children’s Hospital (SCH)
    Disease:

    Adrenoleukodystrophy

  527. SCMCi001-A

    China Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine (SCMC)
    Disease:

    Normal

  528. SCTi003-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal

  529. SCTCi014-A-1 (IPS17-00056 Crispr clone O5)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  530. SCVIi036-A (SCVI248)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  531. SCVIi037-A (SCVI672)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  532. SCVIi049-A (SCVI104)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  533. SCVIi050-A (SCVI2486)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  534. SCVIi066-A (SCVI2047)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Transthyretin amyloid cardiomyopathy

  535. SCVIi073-A (SCVIi574C2)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  536. SCVIi074-A (SCVIi599C1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  537. SCVIi081-A (SCVI2535)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  538. SCVIi082-A (SCVI2838)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  539. SCVIi083-A (SCVI2655)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  540. SCVIi084-A (SCVI2591)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  541. SDPHi003-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Normal

  542. SDPHi004-A

    China Shandong Provincial Hospital Affiliated to Shandong First Medical University (SDPH)
    Disease:

    Normal

  543. SDUe004-A (KMEB4)

    Denmark University of Southern Denmark (SDU)
  544. SDZFYi001-A

    China Shandong Academy of Occupational Health and Occupational Medicine (SDZFY)
    Disease:

    Normal

  545. SHCDNi001-A (SHCDN001)

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Mitochondrial dna depletion syndrome

  546. SHCDNi002-A (SHCDN002)

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Fg syndrome

    Disease:

    Lujan-fryns syndrome

  547. SHCDNi003-A

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Allan-herndon-dudley syndrome

  548. SHCDNi006-A (SHCDN006)

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Epilepsy

  549. SHCDNRi001-A (IPS-51)

    China Shanghai Children's Hospital, Department of Nephrology and Rheumatology (SHCDNR)
    Disease:

    Alport syndrome

  550. SHEHi002-A (iPS36)

    China Shanghai East Hospital (SHEH)
    Disease:

    Long qt syndrome 8

  551. SHEHDNi002-A (KY03AP)

    China Department of Neurology (SHEHDN)
    Disease:

    Parkinson's disease

  552. SHETi002-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Arrhythmia

  553. SHETi003-A

    China Department of Cardiology, Shanghai Children's Hospital (SHET)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  554. SIAISi011-A (NZM)

    China Shanghai Institute for Advanced Immunochemical Studies (SIAIS) (SIAIS)
    Disease:

    Normal

  555. SIGi001-A-3 (iPSC0028 MAPT P301L C4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  556. SIGi001-A-4 (iPSC0028 MAPT P301L D4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  557. SIGi001-A-5 (iPSC0028 MAPT P301S 1C9C4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  558. SIGi001-A-6 (iPSC0028 MAPT P301S 1B9C9)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  559. SIGi001-A-7 (iPSC0028 MAPT P301S 2G2B7)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  560. SIGi001-A-8 (iPSC0028 MAPT P301S+Ex10+16/Clone 7D11A7)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  561. SIGi001-A-9 (iPSC0028 MAPT P301S+Ex10+16/Clone 7H6A1)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  562. SIGi001-A-10 (iPSC0028 MAPT P301S+Ex10+16/Clone 7G4A8)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  563. SIGi001-A-11 (iPSC0028 MAPT P301S+Ex10+16/Clone 7C6A4 and SAMEA4451118)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  564. SIPDi001-A (Li-Campeau syndrome)

    China Shaanxi Institute of Pediatric Diseases (SIPD)
    Disease:

    Li-campeau syndrome

  565. SJTUXHi001-A

    China Shanghai Xinhua Hospital (SJTUXH)
    Disease:

    Autism

  566. SJTUXHi002-A

    China Shanghai Xinhua Hospital (SJTUXH)
    Disease:

    Autism

  567. SKLRMi001-A

    China State Key Laboratory of Reproductive Medicine, Nanjing Medical University (SKLRM)
    Disease:

    Androgen insensitivity syndrome

  568. SKLRMi001-A-1 (AR repaired iPSCs)

    China State Key Laboratory of Reproductive Medicine, Nanjing Medical University (SKLRM)
    Disease:

    Androgen insensitivity syndrome

  569. SKLRMe001-A

    China State Key Laboratory of Reproductive Medicine, Nanjing Medical University (SKLRM)
  570. SMBCi009-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Familial hypercholesterolemia

  571. SMBCi013-A (WD-iPSC)

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Hepatolenticular degeneration

  572. SMCPGHi001-A (SMCPGHi-ABCA3)

    China The Seven Medical Center of PLA General Hospital (SMCPGH)
    Disease:

    Pulmonary surfactant metabolism dysfunction-3

  573. WAe009-A-74

    China Shenzhen People's Hospital (SPH)
    Disease:

    Long qt syndrome 2

  574. WAe009-A-86

    China Shenzhen People's Hospital (SPH)
    Disease:

    Long qt syndrome 2

  575. WAe009-A-88

    China Shenzhen People's Hospital (SPH)
    Disease:

    Long qt syndrome 2

  576. STBCi004-A (SFC832-03-19)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  577. STBCi004-B (SFC832-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  578. STBCi004-B-1 (SFC832-03-06 LRRK2WT/WT C47)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  579. STBCi004-C (SFC832-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  580. STBCi005-A (SFC833-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  581. STBCi005-B (SFC833-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  582. STBCi005-C (SFC833-03-14)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  583. STBCi006-A (SFC140-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  584. STBCi007-A (SFC855-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  585. STBCi007-B (SFC855-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  586. STBCi007-C (SFC855-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  587. STBCi009-C (SFC801-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  588. STBCi011-C (SFC803-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  589. STBCi012-C (SFC805-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  590. STBCi014-C (SFC808-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  591. STBCi015-C (SFC809-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  592. STBCi016-C (SFC810-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  593. STBCi017-A (SFC811-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  594. STBCi017-B (SFC811-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  595. STBCi017-C (SFC811-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  596. STBCi018-C (SFC815-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  597. STBCi019-C (SFC828-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  598. STBCi023-C (SFC829-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  599. STBCi024-C (SFC831-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  600. STBCi025-C (SFC834-03-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  601. STBCi026-A-3 (SFC840-03-03 LRRK2 WT/R1441C H3)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  602. STBCi026-C (SFC840-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal

  603. STBCi028-C (SFC018-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  604. STBCi031-C (SFC024-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  605. STBCi033-C (SFC084-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal

  606. STBCi035-A (SFC813-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  607. STBCi035-B (SFC813-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  608. STBCi035-C (SFC813-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  609. STBCi037-C (SFC816-03-13)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  610. STBCi038-C (SFC011-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  611. STBCi039-C (SFC062-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal

  612. STBCi040-C (SFC029-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  613. STBCi041-C (SFC081-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  614. STBCi042-C (SFC848-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  615. STBCi043-C (SFC120-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  616. STBCi045-C (SFC039-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  617. STBCi048-C (SFC014-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  618. STBCi049-C (SFC040-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  619. STBCi050-C (SFC041-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  620. STBCi051-C (SFC056-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  621. STBCi052-C (SFC086-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal

  622. STBCi053-C (SFC089-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal

  623. STBCi055-C (SFC026-04-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  624. STBCi056-C (SFC064-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal

  625. STBCi057-C (SFC065-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal

  626. STBCi058-C (SFC012-04-31)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  627. STBCi059-C (SFC015-01-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  628. STBCi060-C (SFC038-07-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  629. STBCi063-C (SFC856-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal

  630. STBCi068-C (SFC035-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  631. STBCi069-C (SFC050-03-20)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  632. STBCi071-C (SFC057-07-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  633. STBCi072-C (SFC058-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  634. STBCi074-C (SFC109-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  635. STBCi075-C (SFC129-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  636. STBCi077-C (SFC136-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  637. STBCi078-C (SFC013-07-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  638. STBCi079-C (SFC045-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  639. STBCi080-C (SFC047-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  640. STBCi081-C (SFC170-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  641. STBCi082-C (SFC888-07-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  642. STBCi084-C (SFC871-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  643. STBCi085-C (SFC866-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  644. STBCi087-C (SFC845-03-11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  645. STBCi088-C (SFC872-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  646. STBCi089-C (SFC868-03-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  647. STBCi091-C (SFC126-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  648. STBCi092-C (SFC049-03-13)

    United Kingdom StemBANCC (STBC)
    Disease:

    Diabetes mellitus

  649. STBCi094-C (BPC321-01-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Drug-induced liver injury

  650. STBCi097-C (SFC055-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  651. STBCi098-C (SFC048-07-17)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  652. STBCi110-A (SFC116-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Age-related macular degeneration

  653. STJUDEi004-A (INS3)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  654. STJUDEi004-A-1 (INS3 Isogenic)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  655. STJUDEi005-A (INS14)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  656. STJUDEi005-A-1 (INS14 Isogenic)

    United States St. Jude Children's Research Hospital (STJUDE)
    Disease:

    Diamond-blackfan anemia

  657. SXMUi001-A (SXMUi002-A-1 and HB-iPSCs)

    China Shanxi Medical University (SXMU)
    Disease:

    Hemophilia b

  658. SXMUi002-A (SXMUi001-A-1 and F8-iPSC)

    China Shanxi Medical University (SXMU)
    Disease:

    Hemophilia a

  659. SZGJMSi001-A (ZLP-2)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Schizophrenia

  660. SZGJMSi002-A (TSQ-1)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Obsessive-compulsive disorder

  661. SZGJMSi003-A (TSH-2)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Normal

  662. SZGJMSi004-A (WJM-1)

    China Research Center of Biological Psychiatry, Suzhou Guangji hospital (SZGJMS)
    Disease:

    Depression

  663. TAUi001-A (UTA.09703.HCMJp)

    Finland Tampere University (TAU)
    Disease:

    Hypertrophic cardiomyopathy

  664. TAUi001-A-1 (JPH2)

    Finland Tampere University (TAU)
    Disease:

    Hypertrophic cardiomyopathy

  665. TAUi003-A (UTA.11505.WTsb)

    Finland Tampere University (TAU)
    Disease:

    Normal

  666. TAUi004-A (UTA.05208.CPVT)

    Finland Tampere University (TAU)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  667. TAUi005-A (UTA.14511.CPVT)

    Finland Tampere University (TAU)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  668. TISSUi001-A (HUMIMIC101, StemUse101 and SU101)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal

  669. TUSMi001-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Normal

  670. TUSMi002-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Normal

  671. TUSMi003-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  672. TUSMi004-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsessive-compulsive disorder

  673. TUSMi005-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsolete_bipolar disorder

  674. TUSMi006-A (15M0014)

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsolete_alzheimer's disease

  675. TUSMi007-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  676. TUSMi008-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  677. UAZTi011-A (MKAZ3)

    United States University of Arizona (UAZT)
    Disease:

    Pontocerebellar hypoplasia type 1b

  678. UBi001-A-1

    Spain University of Barcelona (UB)
    Disease:

    Sanfilippo syndrome type c

  679. UBi001-A-2

    Spain University of Barcelona (UB)
    Disease:

    Sanfilippo syndrome type c

  680. UBCi002-A

    Canada University of British Columbia (UBC)
    Disease:

    Leukodystrophy, hypomyelinating, 22

  681. UCLi003-A (TSM(exon10+16)V97)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  682. UCLi004-C (RCi172 and RCFB60c2)

    United Kingdom University College London (UCL)
    Disease:

    Amyotrophic lateral sclerosis

    Disease:

    Frontotemporal dementia

  683. UCLi005-A (LGMD2D Pt. 4 and LGMD2D #4)

    United Kingdom University College London (UCL)
    Disease:

    Limb-girdle muscular dystrophy

  684. UCLi006-A (LCMD-L302P-UCL01C2)

    United Kingdom University College London (UCL)
    Disease:

    Congenital muscular dystrophy due to lmna mutation

  685. UCLi021-A (CLN5c.335G>A;619T>C and 484Pb)

    United Kingdom University College London (UCL)
    Disease:

    Cln5

  686. UCLi022-A (546Pa and CLN5c.1072-1073delTT)

    United Kingdom University College London (UCL)
    Disease:

    Cln5

  687. UCSCi001-A (SII-1802)

    Italy UniversitĂ  Cattolica del Sacro Cuore- Fondazione Policlinico Universitario "A. Gemelli" IRCCS (UCSC)
    Disease:

    Amyotrophic lateral sclerosis

  688. UCSCi002-A (LIF-1989)

    Italy UniversitĂ  Cattolica del Sacro Cuore- Fondazione Policlinico Universitario "A. Gemelli" IRCCS (UCSC)
    Disease:

    Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia

  689. WAe001-A-10 (H1_RB1ex3_G3)

    Germany UniversitÀt Duisburg-Essen (UDE)
    Disease:

    Retinoblastoma

  690. UGENTi001-A (UGENT-MFS003)

    Belgium Ghent University (UGENT)
    Disease:

    Marfan syndrome

  691. UGENTi001-A-1 (UGENT-MFS003-CRISPR)

    Belgium Ghent University (UGENT)
    Disease:

    Marfan syndrome

  692. UHOMi001-A (iPCD02.30)

    France University Hospital of Montpellier (UHOM)
    Disease:

    Primary ciliary dyskinesia

  693. UKAi001-C (hsc3_hiPS_40 and iPS3)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  694. UKAi001-C-1 (hsc3_hiPS_40_16_6 and IRF8-/- iPS3)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  695. UKAi002-A (PBMNC2_hiPS_007 and PV1 JAK2)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  696. UKAi002-A-1 (PV1 JAK2 : CXCL4 KO)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  697. UKAi002-B (PBMNC2_hiPS_009 and PV1 JAK2 V617F het)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  698. UKAi002-B-1 (PV1 JAK2 V617F het : CXCL4 KO)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  699. UKAi003-A (hsc4_hiPS_021 and PV2 JAK2 V617F hom)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  700. UKAi003-A-1 (PV2 JAK2 V617F het)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  701. UKAi003-A-2 (PV2 JAK2)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  702. UKAi004-A (P4_wt4 and patient 1 control 1)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  703. UKAi004-B (patient 1 control 2 and P4_wt8)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  704. UKAi004-C (P4_mut13 and patient 1 D816V 1)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  705. UKAi004-D (P4_mut28 and patient 1 D816V 2)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  706. UKAi004-E (P4_mut30 and patient 1 D816V 3)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  707. UKAi007-A (P13_wt5 and Patient 2 control 1)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  708. UKAi007-B (P13_mut1 and Patient 2 D816V 1)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  709. UKAi008-A (Patient 3 control 1 and P15_wt37)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  710. UKAi008-B (Patient 3 control 2 and P15_wt108)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  711. UKAi008-C (Patient 3 D816V 1 and P15_mut131)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  712. ESIBIe003-A-8 (KIT D816V ESC 1)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  713. ESIBIe003-A-9 (KIT D816V ESC 2)

    Germany UniversitÀtsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  714. UKBi001-B

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Spinocerebellar ataxia type 3

  715. UKBi003-A (iLB-MJD1-32m-r9 and LB-32-r9)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Spinocerebellar ataxia type 3

  716. UKBi005-A (iLB-C-31f-r1 and LB-31-1)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal

  717. UKBi006-A (iLB-C-35m-r1 and LB-35-1)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal

  718. UKBi007-A (LB-33-5 and iLB-MJD3-33f-r5)