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

Search results

Sort by:

Filter by:

  1. ABi001-A

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

    Cone dystrophy with supernormal rod response

  2. ABi002-A

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

    Cone dystrophy with supernormal rod response

  3. AHMUi001-A

    China dongmei ji (AHMU)
    Disease:

    Leber hereditary optic neuropathy

  4. AHQUi001-A (IPS35-2)

    China Affiliated Hospital of Qingdao University (AHQU)
    Disease:

    Non rare in europe: hyperlipoproteinemia type 4

  5. AIBNi015-A (SPG1-AU01C15)

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

    Hereditary spastic paraplegia 56

  6. AIBNi016-A (SPG2-S376C1)

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

    Hereditary spastic paraplegia 56

  7. AIBNi017-A (SPGh1-S075mC2)

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

    Hereditary spastic paraplegia 56

  8. AIBNi018-A (SPGh2-S964pC6)

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

    Hereditary spastic paraplegia 56

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

  59. AMUFAHi002-A (AY20210813)

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

    Polycystic ovary syndrome

  60. AMUFAHi003-A

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

    Normal

  61. WAe009-A-89

    China Anzhen Hospital (ANZHEN)
    Disease:

    Sorsby fundus dystrophy

  62. ATCi002-A

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

    Keipert syndrome

  63. BBANTWi008-A (iPSC_PBMC_LDS_SMAD3_T1_C11)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 3

  64. BBANTWi009-A

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Meester-loeys syndrome

  65. BBANTWi010-A (iPSC_PBMC_LDS_TGFB3_KE2M_C9)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 5

  66. BCHNi001-A (BCHi001-A)

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

    Bardet-biedl syndrome

  67. BCHNCi001-A

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

    Early infantile epileptic encephalopathy

  68. BCRTi006-A

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

    Focal segmental glomerulosclerosis

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

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  70. BIHi004-A (NHDF Epi5 Cl5 iPSC)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  71. BIHi005-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal

  72. BIHi009-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  73. BIHi010-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  74. BIHi015-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  75. BIHi016-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  76. BIHi017-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  77. BIHi018-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  78. BIHi024-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  79. BIHi025-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Focal segmental glomerulosclerosis

  80. BIOi002-A

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Autosomal dominant optic atrophy

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

    China Beijing Institute of Ophthalmology (BIO)
    Disease:

    Hereditary retinal dystrophy

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Huntington disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

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

    Denmark Bioneer (BION)
    Disease:

    Normal

  95. 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

  96. 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

  97. 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

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

    Denmark Bioneer (BION)
    Disease:

    Normal

  99. BJTTHi001-A

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Normal

  100. BJTTHi001-A-3

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  101. BJTTHi001-A-4

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  102. BJTTHi001-A-5

    China Beijing Tiantan Hospital (BJTTH)
    Disease:

    Epilepsy

  103. BRCi021-A (TUH1)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Cardiomyopathy

  104. CBCHi001-A-1

    China Beijing Chest Hospital (CBCH)
    Disease:

    Hypertrophic cardiomyopathy

  105. CBDTi001-A

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

    Normal

  106. CBIGi001-A (AIW002-02)

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

    Normal

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Normal

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

  119. CCMi007-A (SAS1 C5)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  120. CCMi008-A (SAS2 C1)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  121. CCMi009-A (SAS3 C10)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  122. CCMi011-A (SAS7 C6)

    Italy Centro Cardiologico Monzino IRCCS (CCM)
    Disease:

    Covid-19 infection

  123. CHCMUi001-A

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

    Activated pi3k-delta syndrome

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

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

    Transient abnormal myelopoiesis associated with down syndrome

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

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

    Transient abnormal myelopoiesis associated with down syndrome

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

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

    Transient abnormal myelopoiesis associated with down syndrome

  127. CHULAi001-A (GPDi001-A)

    Thailand Chulalongkorn University (CHULA)
    Disease:

    Glucose-6-phosphate dehydrogenase deficiency

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

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

    Catecholaminergic polymorphic ventricular tachycardia 2

  129. 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

  130. CIPi001-A

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

    Benign familial infantile epilepsy

  131. CIPi002-A

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

  132. CMCi006-A-1 (CMC-Fb001(A4GALT-KO))

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

  133. CMFTe004-A (Man-16)

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

    Normal

  134. CMGANTi003-A (SEMD1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  135. CMGANTi004-A (SEMD2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  136. CMGANTi005-A (iPSC_MFS_FBN1_MCE-KB_C8)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Marfan syndrome

  137. CMGANTi006-A (SEDC1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Spondyloepiphyseal dysplasia congenita

  138. CMGANTi007-A (SEDC2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Spondyloepiphyseal dysplasia congenita

  139. CPGHi004-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal

  140. CPGHi006-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Autosomal dominant polycystic kidney disease

  141. CPGHi007-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal

  142. CPGHi008-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Autosomal recessive polycystic kidney disease

  143. CRICKi001-A (iFCI001)

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

    Intellectual disability

  144. CRICKi002-A (iFCI027)

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

    Intellectual disability

  145. CRICKi004-A (iFCI008)

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

    Spinal muscular atrophy with lower extremity predominant

  146. CRICKi005-A (iFCI004)

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

    Spinal muscular atrophy

  147. CRICKi006-A (iFCI005)

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

    Spinal muscular atrophy

  148. CRICKi007-A (iFCI009)

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

    Spinal muscular atrophy with lower extremity predominant

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

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

    X-linked centronuclear myopathy

  150. CRICKi009-A (iFCI012)

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

    Vhl

  151. CRICKi010-A (iFCI013)

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

    Vhl

  152. CRICKi011-A (iFCI016)

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

    Young-onset parkinson disease

  153. CRICKi012-A (iFCI017)

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

    Young-onset parkinson disease

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

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

    Normal

  155. CRTDi006-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  156. CRTDi006-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  157. CRTDi007-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  158. CRTDi007-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 1

  159. CRTDi008-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  160. CRTDi009-A

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  161. CRTDi010-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  162. CRTDi011-A (IDP52555 #9)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  163. CRTDi011-B (IDP52555 #13)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  164. CRTDi011-C (IDP52555 #36)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  165. CRTDi011-D (IDP52555 #44)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal

  166. CSSi013-A

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

    Normal

  167. CSSi014-A

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

    Mucopolysaccharidosis ii

  168. CSSi015-A (FC17)

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

    Normal

  169. CSSi016-A

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

    Charcot-marie-tooth disease type 4b3

  170. CSUXHEi001-A

    China Central South University (CSUXHE)
    Disease:

    Normal

  171. CSUXHEi002-A

    China Central South University (CSUXHE)
    Disease:

    Normal

  172. CTEFe001-A (MUCG01)

    Czech Republic Cell and Tissue Engineering Facility (CTEF)
    Disease:

    Normal

  173. CTEFe002-A (MUCG02)

    Czech Republic Cell and Tissue Engineering Facility (CTEF)
    Disease:

    Normal

  174. CTEFe003-A (MUCG03)

    Czech Republic Cell and Tissue Engineering Facility (CTEF)
    Disease:

    Normal

  175. CTGUi001-A (FD01 and F01)

    China China Three Gorges University (CTGU)
    Disease:

    Fabry disease

  176. WAe001-A-95 (CTU-hES-1)

    China GIBH (CTU)
    Disease:

    Microcephaly-capillary malformation syndrome

  177. CUBi001-A

    Germany Charité - Universitätsmedizin Berlin (CUB)
    Disease:

    Mirage syndrome

  178. CUIMCi005-A (BB#2 and BB9068#2)

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

    Stargardt disease

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

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

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

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

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

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

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

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal

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

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal

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

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal

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

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

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

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

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

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  188. DMBi001-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Normal

  189. DMBi001-A-2

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Normal

  190. DMBi003-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Rheumatoid arthritis

  191. DMBi004-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Rheumatoid arthritis

  192. DPNJMUi001-A

    China Children's Hospital of Nanjing Medical University (DPNJMU)
    Disease:

    Combined oxidative phosphorylation deficiency 23

  193. EDi020-A (SFCi55)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

  194. EDi046-A

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_alzheimer's disease

  196. ESi091-A (HLA91-MiPS4F3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  197. ESi092-A (HLA98-MiPS4F15)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

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

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal

  202. FDCHi007-A

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

    Developmental and epileptic encephalopathy 31

  203. FDCHi008-A (JYIPS0087)

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

    Chronic intestinal pseudoobstruction

  204. FDCHDPe012-A (P4HA2-KO)

    China Fudan University (FDCHDP)
    Disease:

    Normal

  205. FDHPIi001-A

    China (WITHDRAWN) Fudan University (FDHPI)
    Disease:

    Neurodegeneration

  206. 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

  207. FHUSTCi002-A

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

    Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome

  208. FJMUNi001-A

    China Department of Neurology, Fujian Institute of Neurology, the First Affiliated Hospital, Fujian Medical University (FJMUN)
    Disease:

    Duchenne muscular dystrophy

  209. FJMUUHi001-A

    China Fujian Medical University Union Hospital (FJMUUH)
    Disease:

    Parkinson's disease 7

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

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

    Normal

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

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

    Normal

  212. 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

  213. GENYOi007-A (W8)

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

    Meniere disease

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

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

    Parkinson's disease

  215. WAe001-A-77 (H1 RYBP-FLAG-HA KI)

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

    Normal

  216. GWCMCi001-A (iPS-57)

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

    Iga glomerulonephritis

  217. GWCMCi005-A (GWCMCi-TANC2)

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

    Lennox-gastaut syndrome

  218. HADe002-A (HAD 2)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Cystic fibrosis

  219. HEBHMUi008-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Cerebrovascular disease

  220. HEBHMUi012-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Hypertension

  221. HEBHMUi013-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Alzheimer's disease

  222. HHUi003-B (A4_C1)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Maternally-inherited leigh syndrome

  223. HHUi003-C (A4_W1)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Maternally-inherited leigh syndrome

  224. HHUi006-A (11656_H)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Normal

  225. HHUi006-B (11656_K)

    Germany Universitätsklinikum Düsseldorf (HHU)
    Disease:

    Normal

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

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

    Normal

  227. HHUUKDi009-A (TFBJ)

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

    Normal

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

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

    Alpha-1 antitrypsin deficiency

  229. HHUUKDi012-A (AATD iPSC-2 and ISRM-AATD-iPSC-2)

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

    Alpha-1 antitrypsin deficiency

  230. HMSCATi003-A

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

    Parkinson disease

  231. HUJIi001-A (iWSM-F1)

    Israel Hebrew University of Jerusalem (HUJI)
    Disease:

    Developmental and epileptic encephalopathy, 28

  232. HUJIi002-A (iWSM-M2)

    Israel Hebrew University of Jerusalem (HUJI)
    Disease:

    Developmental and epileptic encephalopathy, 28

  233. HUJIi003-A (iWSM-S5)

    Israel Hebrew University of Jerusalem (HUJI)
    Disease:

    Developmental and epileptic encephalopathy, 28

  234. IAIi002-A (IAIi002RSTS1-34-A)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  235. IAIi005-A (AC52)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Normal

  236. IAIi006-A (BC6)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Amyotrophic lateral sclerosis

  237. IAIi007-A (CC5)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Amyotrophic lateral sclerosis

  238. IAIi008-A (DC2)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Amyotrophic lateral sclerosis

  239. IAIi009-A (EC1)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Normal

  240. IAIi010-A (Kif5A 1847 C3)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Autosomal dominant spastic paraplegia type 10

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

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  242. IBBISTi004-B (AS-GB clone 20)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

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

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  244. 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

  245. IBMSi027-A (IBMS-iPSC-073-01)

    Taiwan Institute of Biomedical Sciences, Academia Sinica (IBMS)
    Disease:

    Wolfram syndrome

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

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

    Cystic fibrosis

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

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

    Cystic fibrosis

  248. IBTCMi001-A (NDC1)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Normal

  249. IBTCMi002-A (NDC2)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Normal

  250. IBTCMi003-A (AD1)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Alzheimer's disease

  251. IBTCMi004-A (AD2)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Alzheimer's disease

  252. IBTCMi005-A (AD3)

    China Institute of Basic Theory for Chinese Medicine (IBTCM)
    Disease:

    Alzheimer's disease

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

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

    Normal

  254. ICGi008-A (m55Alz-9L)

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

    Obsolete_alzheimer's disease

  255. ICGi008-B (m55Alz-15L)

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

    Obsolete_alzheimer's disease

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

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

    Hypertrophic cardiomyopathy

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

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

    Hypertrophic cardiomyopathy

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

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

    Hypertrophic cardiomyopathy

  259. ICGi033-A (77Q-17)

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

    Huntington disease

  260. ICGi033-B (77Q-9)

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

    Huntington disease

  261. ICGi033-C (77Q-20)

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

    Huntington disease

  262. ICGi039-A (PD31-6)

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

    Normal

  263. ICGi039-B (PD31-7)

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

    Normal

  264. ICGi039-C (PD31-15)

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

    Normal

  265. ICGi040-A (iTAF16-3)

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

    Infertility

  266. ICGi042-A (PD12-4Lm)

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

    Parkinson's disease

  267. ICGi042-B (PD12-5Lm)

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

    Parkinson's disease

  268. ICGi042-C (PD12-6Lm)

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

    Parkinson's disease

  269. ICGi043-A (LR-21)

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

    Parkinson's disease

  270. ICGi043-B (LR-2)

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

    Parkinson's disease

  271. ICGi043-C (LR-15)

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

    Parkinson's disease

  272. ICGi044-A (PD40-7)

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

    Parkinson's disease

  273. ICGi044-B (PD40-8)

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

    Parkinson's disease

  274. ICGi044-C (PD40-13)

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

    Parkinson's disease

  275. ICSSUi002-A

    China Institute for Cardiovascular Science of Soochow University (ICSSU)
    Disease:

    Aortic dissection

  276. IDIBGIi001-A (GPG1-C23)

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

    Normal

  277. IDIBGIi002-A (RB20234)

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

    Brugada syndrome

  278. IDIBGIi003-A (​RB20235)

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

    Brugada syndrome

  279. IDIBGIi004-A (RB20236)

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

    Brugada syndrome

  280. IDIBGIi005-A (RB20237)

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

    Normal

  281. IIMCBi003-A (K-Pic1)

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

    Normal

  282. IIMCBi004-A (PM-H1)

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

  283. IIMCBi005-A (EM-K3)

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

  284. IIMCBi006-A (M-T1)

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

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

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

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal

  288. INNDSUi001-A (186-Nml-F-24)

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

    Normal

  289. INNDSUi003-A

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

    Becker muscular dystrophy

  290. IOBi001-A (F49B7 and 01F49i-N-B7)

    Switzerland Institute of Molecular and Clinical Ophthalmology Basel (IOB) (IOB)
    Disease:

    Normal

  291. IRFMNi001-A (iPS clone IV)

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

    Normal

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

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

    Normal

  293. IRFMNi002-A (PRM#14)

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

    Focal segmental glomerulosclerosis

  294. IRFMNi002-B (PRM#18)

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

    Focal segmental glomerulosclerosis

  295. IRMBi002-A (AD-APP hiPSC)

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

    Obsolete_alzheimer's disease

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

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

    Normal

  297. 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

  298. ISFi003-A (D2)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Van maldergem syndrome 1

  299. ISFi004-A (F1)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Van maldergem syndrome 1

  300. ITXi001-A (hERG CT Cl9)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  301. ITXi001-A-1 (GPR146KO Cl2)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  302. ITXi002-A (IRX5-Wt and H166Wt C09)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  303. ITXi002-A-1 (CRISPR-2 IRX5 F12 Het and IRX5-Het)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  304. ITXi002-A-2 (CRISPR-2 IRX5 D8 KO and IRX5-KO)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  305. ITXi002-A-3 (IRX5-KI and CRISPR-3 IRX5 F6 KI)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  306. ITXi003-A (MS368)

    France l’institut du thorax (ITX)
    Disease:

    Long qt syndrome

  307. ITXi004-A (MS381)

    France l’institut du thorax (ITX)
    Disease:

    Long qt syndrome

  308. ITXi005-A (MS573)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  309. ITXi006-A (WT8288)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  310. ITXi007-A (202CT)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  311. ITXi008-A (SD378M)

    France l’institut du thorax (ITX)
    Disease:

    Normal

  312. ITXi009-A (CPVT068)

    France l’institut du thorax (ITX)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  313. ITXi010-A (CPVT249)

    France l’institut du thorax (ITX)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  314. ITXi011-A (CPVT033)

    France l’institut du thorax (ITX)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  315. IUFi002-A

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

    Leigh syndrome

  316. JNCSRe002-A-1 (BJNhem20-OCIAD2-CRISPR-33)

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

    Normal

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

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

    Normal

  318. JNCSRe002-A-3 (BJNhem20 OCIAD2-OV)

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

    Normal

  319. JTUi004-A

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

    Otosclerosis

  320. JUCGRMi001-A (VPS35A4)

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

    Parkinson's disease

  321. JUCGRMi001-B (VPS35A5)

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

    Parkinson's disease

  322. JUCGRMi001-C (VPS35A8)

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

    Parkinson's disease

  323. JUCTCi018-A

    Jordan the University of Jordan / Cell Therapy center (JUCTC)
    Disease:

    Charcot-marie-tooth disease

  324. JUCTCi019-A

    Jordan the University of Jordan / Cell Therapy center (JUCTC)
    Disease:

    Charcot-marie-tooth disease type 2

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

  329. WAe001-A-86 (H1.139 and H1.1-39)

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

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

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

    Normal

  338. KEIOi005-A (KAD-0001 and EK-0076)

    Japan Keio University (KEIO)
    Disease:

    Alzheimer's disease

  339. KEIUi002-A (KOMENT-A)

    Japan Keio University (KEIU)
    Disease:

    Normal

  340. KEIUi003-A (KOMENT-B)

    Japan Keio University (KEIU)
    Disease:

    Normal

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

    South Korea Korea Institute of Toxicology (KIT)
    Disease:

    Normal

  342. KLRMMEi001-A

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

    Retinitis pigmentosa

  343. KLRMMEi003-A

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

    Usher syndrome

  344. KMUGMCi003-A (KMUGMCi003ERCC2 and KN610)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Trichothiodystrophy 1, photosensitive

  345. KMUGMCi004-A (KMUGMCi004APC and KN615)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Familial adenomatous polyposis

  346. KMUGMCi005-A (KMUGMCi005TMC8 and KN627)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Epidermodysplasia verruciformis

  347. KMUGMCi007-A (KMUGMCi007PEPD and KN649)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Prolidase deficiency

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

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

    Normal

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

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

    Normal

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

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

    None

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

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

    None

  352. KSCBi012-A (NU01-EiPS07)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal

  353. KUCFRi005-A

    South Korea Korea University Cell Function Regulation Lab (KUCFR)
    Disease:

    Normal

  354. KUCFRi005-A-1

    South Korea Korea University Cell Function Regulation Lab (KUCFR)
    Disease:

    African swine fever virus

  355. KUIMSe001-A (KhES-1)

    Japan Kyoto University (KUIMS)
    Disease:

    Normal

  356. SIGi001-A-21 (SIGi001-AAVS1-FRT)

    Belgium KU Leuven (KUL)
    Disease:

    Normal

  357. SIGi001-A-22 (SIGi001-ICAM1-GFP)

    Belgium KU Leuven (KUL)
    Disease:

    Normal

  358. SIGi001-A-23 (SIGi001-HC3x)

    Belgium KU Leuven (KUL)
    Disease:

    Normal

  359. SIGi001-A-24 (SIGi001-HC3x-ICAM1-GFP)

    Belgium KU Leuven (KUL)
    Disease:

    Normal

  360. KULi003-A

    Belgium KU Leuven (KUL)
    Disease:

    Normal

  361. KUMi004-A

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

    Chronic lymphocytic leukemia

  362. KUMi005-A

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

    Multiple myeloma

  363. KUMi006-A

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

    Multiple myeloma

  364. LCPHi001-A

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

    Obsolete_parkinson's disease

  365. LCPHi002-A

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

    Parkinson's disease

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

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

    Parkinson's disease

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

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

    Parkinson's disease

  368. 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

  369. 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

  370. LCSBi008-A (delP and DJ-1-delP)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson's disease

  371. LCSBi008-A-1 (delP GC13 and DJ-1-delP GC13)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson's disease

  372. LSCTRi006-A (LSCTR-LiPSC-4 and i4)

    South Korea Laboratory of Stem Cells and Tissue Regeneration (LSCTR)
    Disease:

    Normal

  373. LSCTRi007-A (LSCTR-LiPSC-5 and i5)

    South Korea Laboratory of Stem Cells and Tissue Regeneration (LSCTR)
    Disease:

    Normal

  374. LUMCi002-A (113-6 and LUMC0113iATAX06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

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

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

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

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

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

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal

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

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

    Normal

  379. LZUSHi002-A

    China Lanzhou University Second Hospital (LZUSH)
    Disease:

    Madd

  380. MCRIi004-A (PB004)

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

    Normal

  381. MCRIi005-A (PB005)

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

    Normal

  382. MCRIi006-A (PB006)

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

    Normal

  383. MCRIi010-A (PB010)

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

    Normal

  384. MCRIi025-A (CANVAS1-2)

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

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  385. MCRIi025-B (CANVAS1-2 Het GC)

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

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  386. MCRIi026-A (CANVAS3-2)

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

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  387. MCRIi026-B (CANVAS3-2 Het GC)

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

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  388. MCRIi027-A (CANVAS4-6)

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

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  389. MCRIi027-B (CANVAS4-6 Het GC)

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

    Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome

  390. MDCi007-A (8993-A12)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  391. MDCi008-A (8993-B12)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  392. MDCi009-A (8993-C11)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  393. MDCi010-A (8993-D7)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

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

    Taiwan Mackay Medical College (MMC)
    Disease:

    Hearing loss

  395. MPIPi057-A (UL1)

    Germany Max Planck Institute of Psychiatry (MPIP)
    Disease:

    Progressive myoclonic epilepsy type 1

  396. MPIPi058-A (UL4)

    Germany Max Planck Institute of Psychiatry (MPIP)
    Disease:

    Progressive myoclonic epilepsy type 1

  397. MRIi001-A-1 (C6-AAVS1-iCasRx)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal

  398. MRIi003-A-7 (HK-AAVS1-iCasRx)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal

  399. MRIi003-A-8 (HK-AAVS1-CAG-eGFP-homo)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal

  400. MRIi003-A-9 (HK-AAVS1-CAG-FRT-stop-FRT-mKate2-hetero)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal

  401. MRIi005-A

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Long qt syndrome 1

  402. MRIi027-A (DMD 01)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Duchenne muscular dystrophy

  403. MUi026-A (MU012.C4)

    Thailand Mahidol University (MU)
    Disease:

    Autosomal dominant polycystic kidney disease

  404. MUi027-A (MU013.C2)

    Thailand Mahidol University (MU)

  405. MUi031-A (Gaucher iPSC3)

    Thailand Mahidol University (MU)
    Disease:

    Gaucher disease type 3

  406. MUi032-A

    Thailand Mahidol University (MU)
    Disease:

    Choroideremia

  407. MUi034-A (homoHbCS iPSC and MU018)

    Thailand Mahidol University (MU)
    Disease:

    Alpha thalassemia

  408. MUNIi018-A (HUVEC-iPSC)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal

  409. MUNIi018-B (HUVEC-hiPSC-macroH2A1.1)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal

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

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal

  411. MUSIi009-A (HDF-iPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal

  412. MUSIi016-A (TyO)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal

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

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Distal renal tubular acidosis

  414. NCBSi003-A (Park14-R741Q-2022)

    India National Center for Biological Sciences (NCBS)
    Disease:

    Autosomal recessive parkinson disease 14

  415. NCBSi004-A (Park14-control-2022)

    India National Center for Biological Sciences (NCBS)
    Disease:

    Normal

  416. WAe009-A-91

    China National Center for Cardiovascular Diseases & Fuwai Hospital (NCCDFW)
    Disease:

    Barth syndrome

  417. WAe009-A-92

    China National Center for Cardiovascular Diseases & Fuwai Hospital (NCCDFW)
    Disease:

    Normal

  418. WAe009-A-93 (NIS-EGFP-Fluc H9)

    China National Center for Cardiovascular Diseases & Fuwai Hospital (NCCDFW)
    Disease:

    Normal

  419. NCHi001-A (LCL-iPSC4802)

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

    Congenital heart disease

  420. NCHi003-A (NCH005)

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

    Pulmonary valve atresia with intact ventricular septum

  421. NCHi006-A (NCH023)

    United States Nationwide Children's Hospital (NCH)

  422. NCHi009-A (NCH78)

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

    Hypoplastic left heart syndrome

  423. NFHHMUi001-A

    China Department of Neurosurgery of The First Affiliated Hospital of Harbin Medical University (NFHHMU)
    Disease:

    Cerebral cavernous malformation

  424. NIHTVBi016-A (HT876D)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  425. NIHTVBi017-A (HT939A)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  426. NIHTVBi018-A (HT940B)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  427. NIHTVBi019-A (HT852)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Leukodystrophy

  428. NIHTVBi019-A-1 (HT852-DC)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Leukodystrophy

  429. NIHTVBi020-A (HT853)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Normal

  430. NIHTVBi021-A (HT854)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Normal

  431. NIHTVBi022-A (HT964)

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Leukodystrophy

  432. NIHTVBi024-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)

  433. NIHTVBi025-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Sting-associated vasculopathy with onset in infancy

  434. NIHTVBi026-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Sting-associated vasculopathy with onset in infancy

  435. NIHTVBi027-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Sting-associated vasculopathy with onset in infancy

  436. NIHTVBi028-A

    United States National Institutes of Health-National Heart, Lung, and Blood Institute (NIHTVB)
    Disease:

    Lyn gene mutation

  437. NIMHi004-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal

  438. NIMHi005-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal

  439. NIMHi006-A

    India National Institute of Mental Health and Neurosciences (NIMH)
    Disease:

    Normal

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

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

    Normal

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

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

    Normal

  442. NMIi011-A (B1.4)

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

    Breast carcinoma

  443. NMIi011-B (B1.6)

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

    Breast carcinoma

  444. NMIi011-C (B1.7)

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

    Breast carcinoma

  445. NMIi011-D (B1.10)

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

    Breast carcinoma

  446. NMIi012-A (DG1)

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

    Breast carcinoma

  447. NMIi012-B (DG2)

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

    Breast carcinoma

  448. NMIi012-D (DG4)

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

    Breast carcinoma

  449. NMIi012-E (DG5)

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

    Breast carcinoma

  450. NSi003-A (NSi-DS)

    India Stem Cell and Neurobiology Lab (NS)
    Disease:

    Down syndrome

  451. NSi003-B (NSi-isoEu)

    India Stem Cell and Neurobiology Lab (NS)
    Disease:

    Down syndrome

  452. NTUHi002-A

    Taiwan National Taiwan University Hospital (NTUH)
    Disease:

    Aceruloplasminemia

  453. NUIGi063-A (EP2003 C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Kcnq2-related epileptic encephalopathy

  454. NUIGi063-B (EP2003 C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Kcnq2-related epileptic encephalopathy

  455. NUIGi063-C (EP2003 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Kcnq2-related epileptic encephalopathy

  456. NUIGi064-A (EP2C003 C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal

  457. NUIGi064-B (EP2C003 C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal

  458. NUIGi064-C (EP2C003 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal

  459. ORIONi002-A (iALS-2)

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

    Sporadic amyotrophic lateral sclerosis

  460. PFIZi013-A (RCi215 and RCFB59 C9)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Amyotrophic lateral sclerosis

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

    Austria Paracelsus Medical University (PMU)
    Disease:

    Severe combined immunodeficiency

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

    Austria Paracelsus Medical University (PMU)
    Disease:

    Severe combined immunodeficiency

  463. PNUSCRi001-A (GBA PD iPSC7)

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

    Parkinson's disease

  464. PNUSCRi002-A (GBA PD iPSC9)

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

    Parkinson's disease

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

    China Peking University First Hospital (PUFH)
    Disease:

    Leukodystrophy

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

    China Peking Union Medical College (PUMC)
    Disease:

    Normal

  467. PUMCHi019-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Autosomal dominant optic atrophy plus syndrome

  468. QBRIi014-A (NDD01 and hiPSC_11080401_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  469. QBRIi015-A (NDD04 and hiPSC_11080404_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  470. QBRIi016-A (NDD05 and hiPSC_11080405_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Autism spectrum disorder

  471. QBRIi017-A (CtrlM and hiPSC_11080402_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal

  472. QBRIi018-A (hiPSC_11080403_c1 and CtrlF)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Normal

  473. RCi007-A (FB70c1 and RCi170)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  474. RCi009-A (Rci201 and FB73c6)

    United Kingdom Roslin Cells (RC)
    Disease:

    Facioscapulohumeral dystrophy

  475. RCMGi002-A (P7L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  476. RCMGi004-A (P6L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  477. RCMGi004-B (P6L8)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  478. RCMGi005-A (P5L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  479. RCMGi005-B (P5L5)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  480. RCMGi008-A (P9L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  481. RCPCMi009-A (IPSRG4S and UEF-3B)

    Finland Federal State Budgetary Institution Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency (RCPCM)
    Disease:

    Normal

  482. SCIKFi001-A (D3-iR-2)

    Indonesia Stem Cell and Cancer Institute, PT. Kalbe Farma Tbk. (SCIKF)
    Disease:

    Normal

  483. SCMCi001-A

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

    Normal

  484. SCTi003-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal

  485. SCTCi017-A (IPS15-00006)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Stargardt disease

  486. SCTCi018-A (IPS15-00007)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Stargardt disease

  487. SCVIi030-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  488. SCVIi031-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  489. SCVIi036-A (SCVI248)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  490. SCVIi037-A (SCVI672)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  491. SCVIi049-A (SCVI104)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  492. SCVIi050-A (SCVI2486)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  493. SCVIi055-A (SCVI868 and SCVI-868)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal

  494. SCVIi056-A (SCVI956 and SCVI-956)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal

  495. SCVIi057-A (SCVI-975 and SCVI975)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal

  496. SCVIi059-A (SCVIi2413)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  497. SCVIi060-A (SCVi2506)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  498. SCVIi061-A (SCVI2149C1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome

  499. SCVIi062-A (SCVI2150c1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome

  500. SCVIi066-A (SCVI2047)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Transthyretin amyloid cardiomyopathy

  501. SCVIi073-A (SCVIi574C2)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  502. SCVIi074-A (SCVIi599C1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  503. SDZFYi001-A

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

    Normal

  504. SFMUi001-A

    China Shandong First Medical University (SFMU)
    Disease:

    Usher syndrome type 2

  505. SHCDNi006-A (SHCDN006)

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Epilepsy

  506. SHCDNi007-A

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Pyruvate carboxylase deficiency

  507. SHCDNRi001-A (IPS-51)

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

    Alport syndrome

  508. SHETi003-A

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

    Catecholaminergic polymorphic ventricular tachycardia

  509. SIAISi011-A (NZM)

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

    Normal

  510. SIAISi016-A

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

    Alzheimer's disease

  511. SIAISi019-A

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

    Normal

  512. SIAISi020-A

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

    Mild cognitive impairment

  513. SIAISi021-A

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

    Obsolete_alzheimer's disease

  514. SIGi001-A-12 (iPSC0028 - BiAllelic MAPT_Ex10+16T/Clone 1F5-D12 and SAMEA104237570)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  515. SKLRMi001-A

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

    Androgen insensitivity syndrome

  516. SKLRMe005-A

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

  517. SMBCi010-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Multiple osteochondromas

  518. SMBCi011-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Prader-willi syndrome

  519. SMBCi013-A (WD-iPSC)

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Hepatolenticular degeneration

  520. SMBCi014-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Osteogenesis imperfecta

  521. SMBCi018-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Clubfoot

  522. SMUDHe001-A

    China Southern Medical University (SMUDH)
    Disease:

    Normal

  523. WAe009-A-82

    China Southern Medical University (SMUDH)
    Disease:

    Primary cutaneous amyloidosis

  524. WAe009-A-86

    China Shenzhen People's Hospital (SPH)
    Disease:

    Long qt syndrome 2

  525. WAe009-A-88

    China Shenzhen People's Hospital (SPH)
    Disease:

    Long qt syndrome 2

  526. SPPHIi003-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)

  527. SPPHIi004-A

    China Sichuan Academy of Medical Science & Sichuan Provincial People’s Hospital (SPPHI)
    Disease:

    Alzheimer disease

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

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

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

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

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

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

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

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  532. STBCi009-A (SFC801-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  533. STBCi015-A (SFC809-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  534. STBCi015-B (SFC809-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

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

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  536. STBCi026-A-1 (SFC840-03-03 LRRK2-/-D10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

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

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

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

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  539. STBCi061-A (SFC850-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  540. STBCi065-A (SFC853-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

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

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  542. STBCi076-A (SFC134-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  543. STBCi107-A (SFC104-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  544. STJUDEi004-A (INS3)

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

    Diamond-blackfan anemia

  545. STJUDEi004-A-1 (INS3 Isogenic)

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

    Diamond-blackfan anemia

  546. STJUDEi005-A (INS14)

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

    Diamond-blackfan anemia

  547. STJUDEi005-A-1 (INS14 Isogenic)

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

    Diamond-blackfan anemia

  548. UCSFi001-A-64 (P633L RBM20 iPSCs)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Dilated cardiomyopathy

  549. UCSFi001-A-65

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Dilated cardiomyopathy

  550. SUSMi005-A

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  551. SUSMi005-A-1 (SNCA3X 0KO C1 and SNCA3X 0KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  552. SUSMi005-A-2 (SNCA3X 1KO C2 and SNCA3X 1KO C1)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  553. SUSMi005-A-3 (SNCA3X 2KO C1 and SNCA3X 2KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  554. SUSMi005-A-4 (SNCA3X 3KO C1 and SNCA3X 3KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  555. SUSMi005-A-5 (SNCA3X 4KO C1 and SNCA3X 4KO C2)

    United States Stanford University School of Medicine (SUSM)
    Disease:

    Obsolete_parkinson's disease

  556. SUTCMi001-A

    China Shandong University of Traditional Chinese Medicine (SUTCM)
    Disease:

    Normal

  557. SYSUi005-A

    China Sun Yat-sen University (SYSU)
    Disease:

    Hypertrophic cardiomyopathy

  558. WAe009-A-81 (H9-MSX1-/- cell line)

    China Sun Yat-Sen University, center for stem cell biology and tissue engineering (SYSUSC)
    Disease:

    Tooth agenesis

  559. WAe001-A-81

    China The Seventh Affiliated Hospital (SYSUSH)
    Disease:

    Normal

  560. SYSUTFi001-A

    China The First Affiliated Hospital (SYSUTF)
    Disease:

    Hepatocellular carcinoma

  561. SZGJMSi001-A (ZLP-2)

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

    Schizophrenia

  562. SZGJMSi002-A (TSQ-1)

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

    Obsessive-compulsive disorder

  563. SZGJMSi003-A (TSH-2)

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

    Normal

  564. SZGJMSi004-A (WJM-1)

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

    Depression

  565. TAUi008-A (TAU2106C1.MS)

    Finland Tampere University (TAU)
    Disease:

    Multiple sclerosis

  566. TIGETi001-A (ND1.2)

    Italy San Raffaele Telethon Institute for Gene Therapy (SR-Tiget) (TIGET)
    Disease:

    Normal

  567. TISSUi003-A (HUMIMIC103, StemUse103, SU103)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal

  568. TMOi001-A (Gibco Episomal iPSC Line; A18945)

    United States Thermo Fisher Scientific (TMO)
    Disease:

    Normal

  569. TUSMi001-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Normal

  570. TUSMi002-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Normal

  571. TUSMi003-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  572. TUSMi004-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsessive-compulsive disorder

  573. TUSMi005-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsolete_bipolar disorder

  574. TUSMi006-A (15M0014)

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsolete_alzheimer's disease

  575. TUSMi007-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  576. TUSMi008-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  577. UAMi001-A (PCCA23-FiPS4F8)

    Spain Universidad Autonoma de Madrid (UAM)
    Disease:

    Propionic acidemia

  578. UAMi005-A

    Spain Universidad Autonoma de Madrid (UAM)
    Disease:

    Nonketotic hyperglycinemia

  579. UAZTi009-A (MKAZ1)

    United States University of Arizona (UAZT)
    Disease:

    Normal

  580. UAZTi011-A (MKAZ3)

    United States University of Arizona (UAZT)
    Disease:

    Pontocerebellar hypoplasia type 1b

  581. UBi005-A (BJ_iPSC_SV4F_9)

    Spain University of Barcelona (UB)
    Disease:

    Normal

  582. UCLi004-B (RCFB60c7 and RCi177)

    United Kingdom University College London (UCL)
    Disease:

    Amyotrophic lateral sclerosis

    Disease:

    Frontotemporal dementia

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

    United Kingdom University College London (UCL)
    Disease:

    Cln5

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

    United Kingdom University College London (UCL)
    Disease:

    Cln5

  585. UCSFi001-A (wtc11, Wtc11, WTC, WTC11 and GM25256)

    United States Conklin Lab, Gladstone/UCSF (UCSF)
    Disease:

    Normal

  586. UGENTi001-A (UGENT-MFS003)

    Belgium Ghent University (UGENT)
    Disease:

    Marfan syndrome

  587. UGOTSAi002-B (N1-001iC2)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  588. UGOTSAi003-A (N1-002iC3A)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  589. UGOTSAi003-B (N1-002iC4)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  590. UGOTSAi004-A (N1-003iC3)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  591. UGOTSAi004-B (N1-003iC4)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  592. UGOTSAi005-A (N1-004iC2)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Normal

  593. UGOTSAi005-B (N1-004iC6)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Normal

  594. UGOTSAi006-A (N1-005iC1)

    Sweden The Sahlgrenska Academy at University of Gothenburg (UGOTSA)
    Disease:

    Alzheimer's disease

  595. UHi002-A (HEL13.1 and ALS50)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  596. UHi003-A (ALS75 and HEL15.14)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_amyotrophic lateral sclerosis

  597. UHi004-A (HEL157.1)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  598. UHi004-B (HEL157.3)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  599. UHi005-A (HEL158.1)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  600. UHi005-B (HEL158.2)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  601. WAe009-A-90 (H9_LCCS1)

    Finland University of Helsinki (UH)
    Disease:

    Lethal congenital contracture syndrome 1

  602. WAe001-A-79 (H1_CTR1-mEos4b)

    United States University of Houston - Main Campus (UHMC)
    Disease:

    Normal

  603. UHOMi007-A (SMOK1)

    France University Hospital of Montpellier (UHOM)
    Disease:

    Normal

  604. UIOi002-A (iPSC APOE3/3: Unaffected (Coriell #AG09173, female, Age 75))

    United States University of Oslo (UIO)

  605. UIOi006-A (iPSC APOE4/4: Sporadic AD (Coriell #AG10788, female, Age 87))

    Norway University of Oslo (UIO)

  606. UKAi009-A (BM 102-2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Normal

  607. UKAi010-A (BM 104-12)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Normal

  608. UKAi011-A (BM 106-3)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Normal

  609. UKBi013-A (iLB-C-133bm-s4)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal

  610. UKBi015-B (iLB-C16bm-s16)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal

  611. UKBi016-A (iLB-C107bm-s9)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal

  612. UKBi018-A (iLB-C-106bf-s8)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal

  613. UKERi006-B (UKERi82A-S1-017)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal

  614. UKERi009-A (UKERi33Q-R2-006)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal

  615. UKERi010-A (UKERi7MN-S1-010)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal

  616. UKERi010-A-1 (UKERi7MN-010-1)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal

  617. UKERi010-A-2 (UKERi7MN-010-2)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Normal

  618. UKKi018-A (NP0080-2B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Familial long qt syndrome

  619. UKKi031-A (NP0138-8B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Hypertrophic cardiomyopathy

  620. UKWNLi006-A (GLA-D170N-iPSC-1, FD1089/20 and GLA-508G>A-1)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  621. UKWNLi006-B (GLA-D170N-iPSC-2, GLA-508G>A-2 and FD1089/21)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  622. UKWNLi007-A (GLA-515G>A-1, GLA-C172Y-iPSC-1 and FD1210/1)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  623. UKWNLi007-B (GLA-515-G>A-2, FD1210/2 and GLA-C172Y-iPSC-2)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  624. UMi036-A (ND34263)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Parkinson's disease

  625. UMi038-A

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer disease

  626. UMi038-A-1

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer disease

  627. UMi039-A

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Alzheimer's disease

  628. UMi040-A (SB162-284 cl.1)

    United States University of Miami - Miller School of Medicine (UM)
    Disease:

    Auditory neuropathy spectrum disorder

  629. UMCGi011-A (CTP2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  630. UMCGi011-B (CTP2-C5)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  631. UMCGi011-C (CTP2-C4)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  632. UMICHe001-A (UM134-1 PGD)

    United States University of Michigan (UMICH)

  633. UMILi027-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  634. UMILi028-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  635. UNAMi001-A (IFC-UNAM iPD01-S)

    Mexico Instituto de Fisiología Celular, Universidad Nacional Autónoma de México (UNAM)
    Disease:

    Parkinson's disease

  636. UNIBSi017-A (EDS-iPSC)

    Italy University of Brescia (UNIBS)

  637. UNIPDi005-A

    Italy University of Padova (UNIPD)
    Disease:

    Normal

  638. UNIPVi001-A (COR248 and NG2409)

    Italy Units of Biology and Genetics - University of Pavia (UNIPV)
    Disease:

    Joubert syndrome

  639. UNIZARi001-A (FiPSTK2-2)

    Spain University of Zaragoza (UNIZAR)
    Disease:

    Mitochondrial dna depletion syndrome, myopathic form

  640. UOCi001-A (CIM001.4)

    Australia University of Calgary (UOC)

  641. UOCi002-A (CIM008.6)

    Australia University of Calgary (UOC)

  642. UOHi002-A (UOHi002 with its alternative name as UOHi002SHANK3)

    Israel University of Haifa (UOH)
    Disease:

    Normal

  643. UOHi003-A (UOHi001 with its alternative name as UOHi001SHANK3)

    Israel University of Haifa (UOH)
    Disease:

    Phelan-mcdermid syndrome

  644. UOMi008-A (ACS-hiPSC-HPP2)

    Canada University of Manitoba (UOM)
    Disease:

    Hypophosphatasia

  645. UOMi009-A (ACS-hiPSC-HPP3)

    Canada University of Manitoba (UOM)
    Disease:

    Hypophosphatasia

  646. UOSe001-A (MasterShef1, MShef1 and MstrShef1)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  647. UOSe006-A (Shef-6)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  648. UOSe007-A (MstrShef2, MShef2 and MasterShef2)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  649. UOSe008-A (MstrShef3, MShef3 and MasterShef3)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  650. UOSe009-A (MstrShef4, MShef4 and MasterShef4)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  651. UOSe012-A (MstrShef7, MShef7 and MasterShef7)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  652. UOSe013-A (MstrShef8, MasterShef8 and MShef8)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  653. UOSe014-A (MasterShef10, MShef10 and MstrShef10)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  654. UOSe015-A (MasterShef11, MstrShef11 and MShef11)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  655. UOSe016-A (MasterShef12, MShef12 and MstrShef12)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  656. UOSe017-A (MasterShef13, MstrShef13 and MShef13)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  657. UOSe018-A (MasterShef14, MShef14 and MstrShef14)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal

  658. UOXFi005-B (JR053-6)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal

  659. URi001-A

    Japan University of the Ryukyus (UR)
    Disease:

    Major depressive disorder

  660. URi002-A

    Japan University of the Ryukyus (UR)
    Disease:

    Bipolar disorder

  661. URi004-A

    Japan University of the Ryukyus (UR)
    Disease:

    Normal

  662. URi005-A

    Japan University of the Ryukyus (UR)
    Disease:

    Bipolar disorder

  663. USPi001-A (iPS_LGH_AHDC1_P1)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Xia-gibbs syndrome

  664. USPi002-A (iPS_LGH_AHDC1_P2)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Xia-gibbs syndrome

  665. USPi003-A (iPS_LGH_AHDC1_P3)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Xia-gibbs syndrome

  666. VRFi001-A (VRF-RBiPSC01)

    India VISION RESEARCH FOUNDATION (VRF)
    Disease:

    Retinoblastoma

  667. VRISGi002-A

    Vietnam Vinmec Research Insitute of Stem Cell and Gene Technology (VRISG)
    Disease:

    Normal

  668. VUi013-A (804.3)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  669. VUBe012-A (VUB12)

    Belgium Vrije Universiteit Brussel (VUB)

  670. VUBe021-A

    Belgium Vrije Universiteit Brussel (VUB)

  671. WCHi001-A

    China West China Hospital (WCH)
    Disease:

    Normal

  672. WCHi002-A

    China West China Hospital (WCH)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  673. WCHi003-A

    China West China Hospital (WCH)
    Disease:

    Schizophrenia

  674. WCHi004-A

    China West China Hospital (WCH)
    Disease:

    Normal

  675. WCHi005-A

    China West China Hospital (WCH)
    Disease:

    Bipolar disorder

  676. WCHi006-A

    China West China Hospital (WCH)
    Disease:

    Schizophrenia

  677. WTSIi017-A (HPSI0114i-lexy_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal

  678. WTSIi178-B (HPSI0215i-fawm_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal

  679. WTSIi296-A (HPSI0214i-giju_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal

  680. WTSIi362-A (HPSI0513i-oarz_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal

  681. WTSIi362-B (HPSI0513i-oarz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal

  682. WYUi001-A

    China Wuyi University (WYU)
    Disease:

    Normal

  683. XACHi004-A

    China Xi'an children's hospital (XACH)
    Disease:

    Atrial fibrillation

  684. XWHNi001-A

    China Department of Neurology, Xuan Wu Hospital (XWHN)
    Disease:

    Alzheimer's disease

  685. YCMi006-A

    South Korea College of Medicine (YCM)
    Disease:

    Hypertrophic cardiomyopathy

  686. YCMi007-A

    South Korea College of Medicine (YCM)
    Disease:

    Dilated cardiomyopathy

  687. ZJUi009-A (ZJULLi001-A)

    China Zhejiang University (ZJU)
    Disease:

    Marfan syndrome

  688. ZJUi010-A (ZJULLi002-A and 161103SPYLQTFSDC12)

    China Zhejiang University (ZJU)
    Disease:

    Long qt syndrome

  689. ZJUi011-A (ZJULLi003-A and LSYMYH7iPS)

    China Zhejiang University (ZJU)
    Disease:

    Hypertrophic cardiomyopathy

  690. ZJUi012-A (ZJULLi004-A and ZYLMYBPC3iPS)

    China Zhejiang University (ZJU)
    Disease:

    Hypertrophic cardiomyopathy

  691. WAe009-A-38

    China Zhongshan Ophthalmic Center (ZOC)
    Disease:

    Retinitis pigmentosa

  692. WAe009-A-39

    China Zhongshan Ophthalmic Center (ZOC)
    Disease:

    Retinitis pigmentosa

  693. WAe009-A-B

    China Zhengzhou Central Hospital Affiliated (ZZCH)
    Disease:

    Heart failure

  694. ZZUi010-A (ZZU-iPS-AD-APP-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_alzheimer's disease

  695. ZZUi024-A (ZZU-iPS-AD-APP-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Alzheimer's disease

  696. ZZUi036-A (ZZU-iPS-NIID-NOTCH2NLC-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal

  697. ZZUNEUi010-A (CMF001-A)

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Juvenile amyotrophic lateral sclerosis

  698. ZZUNEUi026-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Hypertrophic cardiomyopathy

  699. ZZUNEUi027-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Long qt syndrome 2

  700. ZZUNEUi028-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Hypertrophic cardiomyopathy

  701. WAe009-A-A

    China ZhengZhou University- The first affiliated hospital(ZZU) (ZZUNEU)
    Disease:

    Dry eye syndrome

  702. WAe009-A-C

    China The Second Affiliated Hospital (ZZUSA)
    Disease:

    Heart failure

  703. ZZUSAHi004-A

    China The Second Affiliated Hospital of Zhengzhou University (ZZUSAH)
    Disease:

    Familial long qt syndrome