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  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