hPSCreg®
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Search results

  1. CEBe034-A (SA002)

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

    Patau syndrome

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

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

    Patau syndrome

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

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

    Patau syndrome

  4. MIZMe015-A (Miz-hES13)

    South Korea MizMedi Hospital (MIZM)
    Disease:

    Patau syndrome

  5. AAKIPSi002-A

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

    Aniridia

  6. ABi002-A

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

    Cone dystrophy with supernormal rod response

  7. ABCRIi002-A (#4C1)

    Portugal Algarve Biomedical Center Research Institute (ABC-Ri) (ABCRI)
    Disease:

    Normal (average)

  8. ABCRIi003-A (#8C3)

    Portugal Algarve Biomedical Center Research Institute (ABC-Ri) (ABCRI)
    Disease:

    Complete trisomy 21 syndrome

  9. ABCRIi004-A (#12C2)

    Portugal Algarve Biomedical Center Research Institute (ABC-Ri) (ABCRI)
    Disease:

    Complete trisomy 21 syndrome

  10. ABCRIi005-A (#16C9)

    Portugal Algarve Biomedical Center Research Institute (ABC-Ri) (ABCRI)
    Disease:

    Normal (average)

  11. WIBRe001-A-26 (WIBR3_DJ1_X1-5DEL_2860)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  12. WIBRe001-A-35 (WIBR3_EWT_S4)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  13. WIBRe001-A-36 (WIBR3_EWT_S5)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  14. WIBRe001-A-37 (WIBR3_EWT_S6)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  15. WIBRe001-A-40 (WIBR3_LRRK2_G2019S_2093_Het)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  16. WIBRe001-A-41 (WIBR3_SNCA_A30P_C8-2)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  17. WIBRe001-A-45 (WIBR3_GBA1_IVS2_Het_3C4B)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  18. WIBRe001-A-48 (WIBR3_SYNJ1_R258Q_Homo_A5-1)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  19. WIBRe001-A-54 (WIBR3_VPS13C_FS_Homo_E10-2)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  20. WIBRe001-A-55 (WIBR3_VPS13C_W395C_Homo_C11-3)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  21. WIBRe001-A-56 (WIBR3_VPS13C_W395C_Homo_C6-2)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  22. WIBRe001-A-57 (WIBR3_VPS13C_W395C_Homo_C3-1)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  23. WIBRe001-A-58 (WIBR3_VPS13C_FS_Homo_H3-1)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  24. WIBRe001-A-59 (WIBR3_VPS13C_A444P_Het_E12-1)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  25. WIBRe001-A-60 (WIBR3_VPS13C_A444P_Homo_C8-2)

    United States Albert Einstein College of Medicine (AECM)
    Disease:

    Parkinson disease

  26. AHJNMUi001-A

    China Affiliated Hospital of Jining Medical University(AHJNMU) (AHJNMU)
    Disease:

    Arrhythmogenic right ventricular cardiomyopathy

  27. AHMUCNi002-A (ABCA7-KO-iPSC)

    China Anhui Medical University (AHMUCN)
    Disease:

    Normal (average)

  28. AHMUCNi004-A (AHMUCN-DS3L)

    China Anhui Medical University (AHMUCN)
    Disease:

    Down syndrome

  29. AIBNi020-A (CN-002-300924-MT)

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

    Phenylketonuria

  30. AIBNi023-A (AIBNCASK01)

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

    Cask-related intellectual disability

  31. AIBNi024-A (AIBNCASK02)

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

    Cask-related intellectual disability

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

  39. UCSFi001-A-M (AICS-0109-056)

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

    Cardiomyopathy

  40. AMUFAHi002-A (AY20210813)

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

    Obsolete_polycystic ovary syndrome

  41. WAe009-A-1F (TSC2-/-)

    China Anzhen Hospital Capital Medical university (ANZH)
    Disease:

    Tuberous sclerosis 2

  42. WAe009-A-2K (PDK1 KO)

    China Anzhen Hospital Capital Medical university (ANZH)
    Disease:

    Diabetes mellitus

  43. AOUMEYi002-A

    Italy Meyer Children's Hospital IRCCS (AOUMEY)
    Disease:

    Gm3 synthase deficiency

  44. ASGRCi006-A (0808 CHR)

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Obsolete_proliferative diabetic retinopathy

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

    Taiwan Genomics Research Center (ASGRC)
    Disease:

    Type 2 diabetes mellitus

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

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

    Normal (average)

  47. AUi001-A

    Denmark Aarhus University (AU)
    Disease:

    Herpes simplex encephalitis

  48. AUMCi001-A (LUMC0195iFOXC)

    Netherlands Amsterdam University Medical Centers (AUMC)

  49. AUMCi006-A (LUMC0196iOAT)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Gyrate atrophy of choroid and retina

  50. AUMCi010-C (LF2A_C04 and LUMC0255iHCM04)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  51. AUMCi010-D (LF2A_C01 and LUMC0255iHCM01)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  52. AUMCi011-C (LUMC0258iHCM05 and LF2B_C05)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  53. AUMCi013-A (LUMC0282iHCM02 and LF3B_C02)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  54. AUMCi013-B (LF3B_C04 and LUMC0282iHCM04)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  55. AUMCi013-C (LF3B_C05 and LUMC0282iHCM05)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  56. AUMCi013-D (LF3B_C03 and LUMC0282iHCM03)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  57. AUMCi013-E (LF3B_C09 and LUMC0282iHCM09)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  58. AUMCi013-F (LF3B_C14 and LUMC0282iHCM14)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  59. AUMCi014-A (LF3C_C02 and LUMC0283iHCM02)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  60. AUMCi014-B (LF3C_C05 and LUMC0283iHCM05)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  61. AUMCi014-H (MF3C_C08)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Hypertrophic cardiomyopathy

  62. AUMCi015-A (LMNA-D44)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Dilated cardiomyopathy

  63. AUMCi015-A-1 (LMNA-D44-PE1-A43B)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Dilated cardiomyopathy

  64. AUMCi016-A (LUMC0277iFBN01)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Marfan syndrome

  65. AUMCi017-A (LUMC0278iFBN04)

    Netherlands Amsterdam University Medical Centers (AUMC)
    Disease:

    Marfan syndrome

  66. WAe009-A-1E (TBX20-KO)

    China Anzhen Hospital (ANZHEN) (AZH)
    Disease:

    Dilated cardiomyopathy

  67. BAFYi001-A

    China Shenzhen Baoan Women's and Children's Hospital (BAFY)
    Disease:

    Edwards syndrome

  68. BBANTWi008-A (iPSC_PBMC_LDS_SMAD3_T1_C11)

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Loeys-dietz syndrome 3

  69. BBANTWi011-A

    Belgium Biobank Antwerpen (BBANTW)
    Disease:

    Familial thoracic aortic aneurysm and aortic dissection

  70. BBSSPAi001-A (Ctrl FiPS1-Sv4F-25)

    Spain Biobanco del Sistema Sanitario Público de Andalucía (BBSSPA)
    Disease:

    Normal (average)

  71. BCHi007-A (HNDS0005-01 #B)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  72. BCHi009-A (HNDS0002-01 #D)

    United States Children's Hospital (BCH)
    Disease:

    Succinic semialdehyde dehydrogenase deficiency

  73. BCHi013-A (HNDS0143-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  74. BCHi013-A-1 (HNDS0143-01#A CNC21(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  75. BCHi013-A-2 (HNDS0143-01#A CNC24(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  76. BCHi013-A-3 (HNDS0143-01#A CC12(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  77. BCHi013-A-4 (HNDS0143-01#A CC28(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  78. BCHi017-A (HNDS0164-01#D)

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  79. BCHi018-A-1 (HNDS0176-01#A CNC10(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  80. BCHi019-A-2 (HNDS0179-01#B CNC21(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  81. BCHi019-A-3 (HNDS0179-01#B CC13(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  82. BCHi019-A-4 (HNDS0179-01#B CC15(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Pten hamartoma tumor syndrome

  83. BCHi021-A-4 (HNDS0129-01#A CNC8(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  84. BCHi022-A (HNDS0108-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  85. BCHi024-A (HNDS0142-01#D)

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  86. BCHi024-A-4 (HNDS0142-01#D CC16(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Haploinsufficiency

  87. BCHi026-A-3 (HNDS0136-01#A CNC19(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  88. BCHi026-A-4 (HNDS0136-01#A CC23(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  89. BCHi027-A-2 (HNDS0145-01#A CC32-1(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  90. BCHi029-B (HNDS0121-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Tuberous sclerosis complex

  91. BCHi031-A-4 (HNDS0032-01#A CC31(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  92. BCHi033-A (HNDS0060-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  93. BCHi033-A-3 (HNDS0060-01#B CC9(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  94. BCHi034-A (HNDS0181-01#F)

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  95. BCHi034-A-4 (HNDS0181-01#F CC7(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Foxg1 syndrome

  96. BCHi036-A (HNDS0070-01#B)

    United States Children's Hospital (BCH)
    Disease:

    Developmental and epileptic encephalopathy 7

  97. BCHi040-A-1 (HNDS0130-01#B CNC8(+/-))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  98. BCHi040-A-4 (HNDS0130-01#B CC67(+/+))

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  99. BCHi043-A (HNDS0056-01#A)

    United States Children's Hospital (BCH)
    Disease:

    Phelan-mcdermid syndrome

  100. BCHNi001-A (BCHi001-A)

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

    Bardet-biedl syndrome

  101. BCHNDi001-A

    China 徐超龙 (BCHND)
    Disease:

    Mitochondrial encephalomyopathy

  102. BCMi002-A (LZ02)

    United States Baylor College of Medicine (BCM)
    Disease:

    Normal (average)

  103. BCRTi004-A

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

    Normal (average)

  104. BCRTi010-A

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

    Normal (average)

  105. BFVSBi003-A

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

    Ehlers-danlos syndrome, vascular type

  106. BFVSBi004-A

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

    Ehlers-danlos syndrome, vascular type

  107. BFVSBi005-A

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

    Covid-19

  108. BFVSBi006-A

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

    Varicose veins

  109. BGUi002-A (BGU02iPOR)

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

    P450 oxidoreductase deficiency

  110. BGUi003-A (BGU03iPOR)

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

    P450 oxidoreductase deficiency

  111. BGUi008-A (DCM-C)

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

    Left ventricular noncompaction cardiomyopathy

  112. BGUi011-A (BGU01iGRIN2D)

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

    Developmental and epileptic encephalopathy, 46

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

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

    Normal (average)

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

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

    Normal (average)

  115. BGUi015-A (BGUiBJ)

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

    Normal (average)

  116. BIHi001-B-1

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  117. BIHi001-B-13

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  118. BIHi004-A (NHDF Epi5 Cl5 iPSC)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  119. BIHi005-A-93

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  120. BIHi006-D

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  121. BIHi008-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  122. BIHi009-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  123. BIHi010-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  124. ZIPi013-B-1 (BIHi257-A-1)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  125. ZIPi013-B-2 (BIHi257-A-2)

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  126. BIHi017-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  127. BIHi025-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  128. BIHi028-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  129. BIHi030-C

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  130. BIHi038-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Obsolete_focal segmental glomerulosclerosis

  131. BIHi044-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Allan-herndon-dudley syndrome

  132. BIHi250-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  133. BIHi266-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  134. BIHi267-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

  135. BIHi269-B

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  136. BIHi276-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Leigh disease

  137. BIHi290-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Normal (average)

  138. BIHi300-A

    Germany Berlin Institute of Health (BIH)
    Disease:

    Chemotherapy-related cognitive impairment

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  156. BIONi010-C-48 (BIONi010-C hMDR1)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  157. 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 (average)

  158. 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 (average)

  159. 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 (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  162. BIONi010-C-70 (BIONi010-C with an APOE 2/2 genotype with an additional, homozygous christchurch mutation)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

  163. BIONi010-C-71 (BIONi010-C with an APOE 3/3 genotype with an additional, homozygous christchurch mutation)

    Denmark Bioneer (BION)
    Disease:

    Alzheimer's disease

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

    Denmark Bioneer (BION)
    Disease:

    Alzheimer disease

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

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

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  173. BIONi033-A (H180615 and SAMEA4563389)

    Denmark Bioneer (BION)
    Disease:

    Normal (average)

  174. BIORTCi001-A (BAiPSC 000 and OSTiFGM2)

    Nigeria Biomedical Science Research and Training Centre (BIORTC)
    Disease:

    Normal (average)

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

    Hungary BioTalentum Ltd. (BIOT)
    Disease:

    Obsolete_alzheimer's disease

  176. UMANe002-A-2

    United Kingdom Birket Lab (BIR)
    Disease:

    Normal (average)

  177. BIUi001-A (T1A1i-001)

    Israel Bar Ilan University (BIU)
    Disease:

    Obsolete: nuclear cell envelopathy

  178. BRCi014-A (1383D6 and HPS1006)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Normal (average)

  179. BRCi025-A (HiPS-RTT_CUH02)

    Japan RIKEN BioResource Research Center (BRC)
    Disease:

    Rett syndrome

  180. BTHBIOi001-A (BiPSC-HXL-CNGA1)

    China Beijing Institute of Ophthalmology for BeijingTongren Hospital (BTHBIO)
    Disease:

    Retinitis pigmentosa

  181. BTHBIOi002-A

    China Beijing Institute of Ophthalmology for BeijingTongren Hospital (BTHBIO)
    Disease:

    Usher syndrome

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

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

    Retinitis pigmentosa

  183. WIBRe001-A-5 (WIBR3_PRKN_X3DEL_F2-5)

    United States University of California, Berkeley (CAL)
    Disease:

    Parkinson disease

  184. WIBRe001-A-10 (WIBR3_FBXO7_FS_A3-1)

    United States University of California, Berkeley (CAL)
    Disease:

    Parkinson disease

  185. WIBRe001-A-13 (WIBR3_PINK1_Q129X_E7-1)

    United States University of California, Berkeley (CAL)
    Disease:

    Parkinson disease

  186. CBi001-A (XLC-348)

    United States Creative Bioarray (CB)
    Disease:

    Obsolete_schizophrenia

  187. CBIGi001-A (AIW002-02 and IPSC0063)

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

    Normal (average)

  188. CBIGi001-A-13 (IPSC0078 and SCARB2-KO/AIW002-02)

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

    Parkinson disease

  189. CBIGi001-A-30 (BIN3-KO/AIW002-02 and IPSC0102)

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

    Parkinson disease

  190. CBIGi002-A (2890 (GBA W378G, heterozygous), 2890 and IPSC0001)

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

    Parkinson disease

  191. CBIGi002-A-1 (GBA W378G-correction/2890, 2890-iso and IPSC0002)

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

    Parkinson disease

  192. CBIGi003-A (3026, 3026 (GBA N370S, heterozygous) and IPSC0004)

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

    Parkinson disease

  193. CBIGi003-A-1 (3026-iso, GBA N370S-correction/3026 and IPSC0005)

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

    Parkinson disease

  194. CBIGi005-A (IPSC0003 and LRRK2 G2019S)

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

    Parkinson disease

  195. CBIGi008-A (IPSC0011 and GBA T369M)

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

    Parkinson disease

  196. CBIGi011-A (SOD1 I114T and IPSC0015)

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

    Amyotrophic lateral sclerosis

  197. CBIGi013-A (IPSC0017 and LRRK2 M1646T (heterozygous))

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

    Parkinson disease

  198. CBIGi013-A-1 (LRRK2 M1646T correction and IPSC0018)

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

    Parkinson disease

  199. CBIGi021-A (GBA1 L324I and IPSC0027)

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

    Parkinson disease

  200. CBIGi034-A (IPSC0045)

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

    Normal (average)

  201. CBIGi035-A (IPSC0046)

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

    Normal (average)

  202. CBIGi038-A (IPSC0049)

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

    Amyotrophic lateral sclerosis

  203. CBIGi041-A (IPSC0053 and GBA L444P (CBIGi041-A))

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

    Parkinson disease

  204. CBIGi048-A (IPSC0092)

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

    Amyotrophic lateral sclerosis

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

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

    Normal (average)

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

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

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

    Myotonic dystrophy type 1

  209. CBRCULi010-A (GM00498E-1 and GM00498E clone 1)

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

    Normal (average)

  210. CBRCULi013-A (GM04602-2 and GM04602 clone 2)

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

    Myotonic dystrophy type 1

  211. CBRCULi014-A (AG09393A clone 3 and AG09393A-3)

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

    Normal (average)

  212. CBRCULi017-A (SCN5A p.R219-22B)

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

    Normal (average)

  213. CBRCULi020-A (79-1761-15)

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

    Myotonic dystrophy type 1

  214. WAe009-A-Q

    Austria St. Anna Kinderkrebsforschung GmbH (CCRI)
    Disease:

    Ewing sarcoma

  215. CDIi001-A (01279)

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

    Normal (average)

  216. CDIi002-A (01434)

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

    Normal (average)

  217. CDIi004-A (11713)

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

    Normal (average)

  218. CDIi013-A (PPMI_3409 and FCDI_11287)

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

    Parkinson disease

  219. CDIi023-A (FCDI_11303 and PPMI_3448)

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

    Parkinson disease

  220. CDIi027-A (FCDI_11308 and PPMI_3186)

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

    Parkinson disease

  221. CDIi030-A (FCDI_11311 and PPMI_3668)

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

    Normal (average)

  222. CDIi059-A (PPMI_52828 and FCDI_11363)

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

    Prodromal period

    Disease:

    Parkinson disease

  223. CDIi069-A (PPMI_3666 and FCDI_11449)

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

    Parkinson disease

  224. CDIi082-A (PPMI_4099 and FCDI_11475)

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

    Parkinson disease

  225. CDIi088-A (PPMI_4107 and FCDI_11492)

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

    Parkinson disease

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

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

    Normal (average)

  227. CEBe012-A (SA121)

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

  228. CEBe013-A (SA142)

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

  229. CEGHUi001-A (iPSC_CEGH_C2)

    Brazil Human Genome and Stem Cell Research Center, University of São Paulo (CEGHU)
    Disease:

    Normal (average)

  230. CENSOi002-B (FB74R2c4 and CENSOi261)

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

    Duchenne muscular dystrophy

  231. CENSOi005-A (FB76R2c5 and CENSOi245)

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

    Duchenne muscular dystrophy

  232. CHCMUi002-A

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

    Chronic granulomatous disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Normal (average)

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

    United States CHDI Foundation Inc. (CHDI)
    Disease:

    Huntington disease

  267. CHINTAi001-A (iCON-001)

    India CHINTA (CHINTA)
    Disease:

    Normal (average)

  268. CHINTAi005-A (iMDD-002 and CUPi005-A)

    India CHINTA (CHINTA)
    Disease:

    Unipolar depression

  269. CHOCi005-A

    United States CHOC Children's (CHOC)
    Disease:

    Gm1 gangliosidosis

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

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

    Transient abnormal myelopoiesis associated with down syndrome

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

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

    Transient abnormal myelopoiesis associated with down syndrome

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

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

    Transient abnormal myelopoiesis associated with down syndrome

  273. CHOPi012-A (CHOPACTG2-R257C)

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

    Obsolete_megacystis-microcolon-intestinal hypoperistalsis syndrome 5

  274. CHOPi013-A (CHOPWT17_TPM1KOc28)

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

    Normal (average)

  275. CHOPi014-A (CHOPWT15)

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

    Normal (average)

  276. CHSUi001-A

    China Children’s Hospital Affiliated to Shandong University, (CHSU)
    Disease:

    Severe combined immunodeficiency

  277. CHSUi002-A

    China Children’s Hospital Affiliated to Shandong University, (CHSU)
    Disease:

    Hatipoglu immunodeficiency syndrome

  278. CHUQi002-A (ARSM44081223)

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

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  279. CHUQi007-A (ARSM47280521)

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

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  280. CHUQi008-A (ARSM42081221)

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

    Autosomal recessive spastic ataxia of charlevoix-saguenay

  281. CHWi001-A

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

    Intellectual disability

  282. CHZJUi001-A

    China Children’s Hospital (CHZJU)
    Disease:

    Dilated cardiomyopathy

  283. CIGLi001-A (RPChiPS8023G1, iPSC TBX4 WT, StemRNA™ Human iPSC 802-3G and SYNTHEGO 802-30F)

    United States Center for Infection and Genomics of the Lung (CIGL)
    Disease:

    Normal (average)

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

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

    Facioscapulohumeral muscular dystrophy 2

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

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

    Facioscapulohumeral muscular dystrophy 2

  286. CIRMi005-A (CW13006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  287. CIRMi011-A (CW13020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  288. CIRMi013-A (CW13023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  289. CIRMi019-A (CW13030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  290. CIRMi023-A (CW13034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  291. CIRMi029-A (CW13045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  292. CIRMi031-A (CW13048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  293. CIRMi033-A (CW13052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  294. CIRMi042-A (CW13067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  295. CIRMi043-A (CW13070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  296. CIRMi044-A (CW13072)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  297. CIRMi045-A (CW13073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  298. CIRMi046-A (CW13074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  299. CIRMi047-A (CW13075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  300. CIRMi048-A (CW13076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  301. CIRMi049-A (CW13077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  302. CIRMi050-A (CW13079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  303. CIRMi051-A (CW13088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  304. CIRMi052-A (CW13092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  305. CIRMi053-A (CW13093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  306. CIRMi054-A (CW13094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  307. CIRMi055-A (CW13095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  308. CIRMi056-A (CW13097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  309. CIRMi057-A (CW13098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  310. CIRMi058-A (CW13105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  311. CIRMi059-A (CW13107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  312. CIRMi060-A (CW13108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  313. CIRMi061-A (CW13109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  314. CIRMi069-A (CW50005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  315. CIRMi073-A (CW50017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  316. CIRMi077-A (CW50057)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  317. CIRMi107-A (CW50013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  318. CIRMi109-A (CW50018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  319. CIRMi120-A (CW50032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  320. CIRMi133-A (CW50045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  321. CIRMi137-A (CW50051)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  322. CIRMi141-A (CW50056)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  323. CIRMi146-A (CW50062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  324. CIRMi147-A (CW50063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  325. CIRMi148-A (CW50064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  326. CIRMi149-A (CW50065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  327. CIRMi150-A (CW50066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  328. CIRMi151-A (CW50067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  329. CIRMi167-A (CW50095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  330. CIRMi178-A (CW50112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  331. CIRMi197-A (CW50134)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  332. CIRMi209-A (CW50149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  333. CIRMi215-A (CW50157)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  334. CIRMi220-A (CW50165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  335. CIRMi226-A (CW50173)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  336. CIRMi227-A (CW50174)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Late-onset alzheimer's disease

  337. CIRMi231-A (CW12000)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypoplasia of the optic nerve

  338. CIRMi232-A (CW12001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  339. CIRMi233-A (CW12002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypoplasia of the optic nerve

  340. CIRMi234-A (CW12003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  341. CIRMi235-A (CW12004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  342. CIRMi236-A (CW80003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  343. CIRMi238-A (CW80008)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  344. CIRMi239-A (CW80009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  345. CIRMi242-A (CW80012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  346. CIRMi245-A (CW80054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  347. CIRMi246-A (CW80018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  348. CIRMi247-A (CW80019)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  349. CIRMi248-A (CW80055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  350. CIRMi254-A (CW80027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  351. CIRMi256-A (CW80030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  352. CIRMi257-A (CW80031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  353. CIRMi258-A (CW80038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  354. CIRMi261-A (CW80042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  355. CIRMi265-A (CW80049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dyskinesia with orofacial involvement

  356. CIRMi266-A (CW80050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  357. CIRMi272-A (CW70007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  358. CIRMi277-A (CW70013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  359. CIRMi291-A (CW70034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  360. CIRMi304-A (CW70048)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  361. CIRMi330-A (CW70092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  362. CIRMi336-A (CW70100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  363. CIRMi337-A (CW70101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  364. CIRMi338-A (CW70102)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  365. CIRMi339-A (CW70103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  366. CIRMi340-A (CW70104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  367. CIRMi341-A (CW70105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  368. CIRMi342-A (CW70106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  369. CIRMi343-A (CW70107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  370. CIRMi344-A (CW70108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  371. CIRMi345-A (CW70109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  372. CIRMi346-A (CW70110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  373. CIRMi347-A (CW70111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  374. CIRMi348-A (CW70112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  375. CIRMi349-A (CW70114)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  376. CIRMi350-A (CW70115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  377. CIRMi351-A (CW70116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  378. CIRMi352-A (CW70117)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  379. CIRMi353-A (CW70118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  380. CIRMi354-A (CW70120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  381. CIRMi355-A (CW70122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  382. CIRMi356-A (CW70123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  383. CIRMi357-A (CW70124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  384. CIRMi358-A (CW70125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  385. CIRMi359-A (CW70127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  386. CIRMi360-A (CW70128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  387. CIRMi361-A (CW70129)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  388. CIRMi362-A (CW70130)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  389. CIRMi363-A (CW70131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  390. CIRMi364-A (CW70132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  391. CIRMi365-A (CW70133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  392. CIRMi366-A (CW70134)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  393. CIRMi367-A (CW70135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  394. CIRMi368-A (CW70137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  395. CIRMi369-A (CW70138)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  396. CIRMi370-A (CW70140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  397. CIRMi371-A (CW70141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  398. CIRMi372-A (CW70142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  399. CIRMi373-A (CW70143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  400. CIRMi374-A (CW70144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  401. CIRMi375-A (CW70151)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  402. CIRMi376-A (CW70152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  403. CIRMi377-A (CW70155)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  404. CIRMi378-A (CW70156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  405. CIRMi379-A (CW70158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  406. CIRMi380-A (CW70160)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  407. CIRMi381-A (CW70161)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  408. CIRMi382-A (CW70164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  409. CIRMi383-A (CW70165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  410. CIRMi384-A (CW70167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  411. CIRMi385-A (CW70168)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  412. CIRMi389-A (CW70173)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  413. CIRMi396-A (CW70182)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  414. CIRMi397-A (CW70010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  415. CIRMi405-A (CW70189)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Primary open angle glaucoma

  416. CIRMi411-A (CW70196)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Age-related macular degeneration

  417. CIRMi438-A (CW70239)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  418. CIRMi460-A (CW70263)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Diabetic retinopathy

  419. CIRMi466-A (CW70270)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  420. CIRMi485-A (CW70297)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  421. CIRMi528-A (CW70353)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 1 diabetes mellitus

  422. CIRMi533-A (CW70359)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Type 2 diabetes mellitus

  423. CIRMi544-A (CW40002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  424. CIRMi545-A (CW40003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  425. CIRMi546-A (CW40004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  426. CIRMi547-A (CW40005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  427. CIRMi548-A (CW40006)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  428. CIRMi549-A (CW40009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  429. CIRMi550-A (CW40010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  430. CIRMi551-A (CW40011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  431. CIRMi552-A (CW40012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  432. CIRMi553-A (CW40013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  433. CIRMi554-A (CW40014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  434. CIRMi555-A (CW40015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  435. CIRMi556-A (CW40017)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  436. CIRMi557-A (CW40018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  437. CIRMi558-A (CW40020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  438. CIRMi559-A (CW40021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  439. CIRMi560-A (CW40022)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  440. CIRMi561-A (CW40023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  441. CIRMi562-A (CW40024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  442. CIRMi563-A (CW40025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  443. CIRMi564-A (CW40026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  444. CIRMi565-A (CW40027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  445. CIRMi566-A (CW40028)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  446. CIRMi567-A (CW40029)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  447. CIRMi568-A (CW40030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  448. CIRMi569-A (CW40031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  449. CIRMi570-A (CW40032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  450. CIRMi571-A (CW40033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  451. CIRMi572-A (CW40034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  452. CIRMi573-A (CW40035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  453. CIRMi574-A (CW40037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  454. CIRMi575-A (CW40038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  455. CIRMi576-A (CW40039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  456. CIRMi577-A (CW40040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  457. CIRMi578-A (CW40042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  458. CIRMi579-A (CW40043)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  459. CIRMi580-A (CW40044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  460. CIRMi581-A (CW40046)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  461. CIRMi582-A (CW40047)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  462. CIRMi583-A (CW40049)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  463. CIRMi584-A (CW40051)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  464. CIRMi585-A (CW40052)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  465. CIRMi586-A (CW40053)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  466. CIRMi587-A (CW40054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  467. CIRMi588-A (CW40055)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  468. CIRMi589-A (CW40057)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  469. CIRMi590-A (CW40061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  470. CIRMi591-A (CW40062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  471. CIRMi592-A (CW40063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  472. CIRMi593-A (CW40064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  473. CIRMi594-A (CW40065)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  474. CIRMi595-A (CW40066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  475. CIRMi596-A (CW40067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  476. CIRMi597-A (CW40068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  477. CIRMi598-A (CW40070)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  478. CIRMi599-A (CW40071)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  479. CIRMi600-A (CW40073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  480. CIRMi601-A (CW40074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  481. CIRMi602-A (CW40075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  482. CIRMi603-A (CW40077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  483. CIRMi604-A (CW40078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  484. CIRMi605-A (CW40079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  485. CIRMi606-A (CW40080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  486. CIRMi607-A (CW40081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  487. CIRMi608-A (CW40083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  488. CIRMi609-A (CW40084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  489. CIRMi610-A (CW40085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  490. CIRMi611-A (CW40086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  491. CIRMi612-A (CW40087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  492. CIRMi613-A (CW40088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  493. CIRMi614-A (CW40089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  494. CIRMi615-A (CW40090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  495. CIRMi616-A (CW40091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  496. CIRMi617-A (CW40092)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  497. CIRMi618-A (CW40094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  498. CIRMi619-A (CW40096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  499. CIRMi620-A (CW40097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  500. CIRMi621-A (CW40100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  501. CIRMi622-A (CW40101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  502. CIRMi623-A (CW40105)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  503. CIRMi624-A (CW40106)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  504. CIRMi625-A (CW40107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  505. CIRMi626-A (CW40109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  506. CIRMi627-A (CW40110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  507. CIRMi628-A (CW40111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  508. CIRMi629-A (CW40112)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  509. CIRMi630-A (CW40113)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  510. CIRMi631-A (CW40114)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  511. CIRMi632-A (CW40115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  512. CIRMi633-A (CW40116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  513. CIRMi634-A (CW40118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  514. CIRMi635-A (CW40119)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  515. CIRMi636-A (CW40120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  516. CIRMi637-A (CW40121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  517. CIRMi638-A (CW40122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  518. CIRMi639-A (CW40123)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  519. CIRMi640-A (CW40124)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  520. CIRMi641-A (CW40125)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  521. CIRMi642-A (CW40126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  522. CIRMi643-A (CW40127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  523. CIRMi644-A (CW40128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  524. CIRMi645-A (CW40129)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  525. CIRMi646-A (CW40131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  526. CIRMi647-A (CW40132)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  527. CIRMi648-A (CW40135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  528. CIRMi649-A (CW40136)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  529. CIRMi650-A (CW40137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  530. CIRMi651-A (CW40139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  531. CIRMi652-A (CW40142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  532. CIRMi653-A (CW40144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  533. CIRMi654-A (CW40145)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  534. CIRMi655-A (CW40147)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  535. CIRMi656-A (CW40148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  536. CIRMi657-A (CW40149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  537. CIRMi658-A (CW40152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  538. CIRMi659-A (CW40153)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  539. CIRMi660-A (CW40157)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  540. CIRMi661-A (CW40159)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  541. CIRMi662-A (CW40160)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  542. CIRMi663-A (CW40161)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  543. CIRMi664-A (CW40163)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  544. CIRMi665-A (CW40164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  545. CIRMi666-A (CW40165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  546. CIRMi667-A (CW40167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  547. CIRMi668-A (CW40169)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  548. CIRMi669-A (CW40172)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  549. CIRMi670-A (CW40174)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  550. CIRMi671-A (CW40178)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  551. CIRMi672-A (CW40181)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  552. CIRMi673-A (CW40182)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  553. CIRMi674-A (CW40183)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  554. CIRMi675-A (CW40185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  555. CIRMi676-A (CW40187)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  556. CIRMi677-A (CW40190)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  557. CIRMi678-A (CW40191)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  558. CIRMi679-A (CW40192)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  559. CIRMi680-A (CW40193)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  560. CIRMi681-A (CW40194)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  561. CIRMi682-A (CW40195)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  562. CIRMi683-A (CW40196)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  563. CIRMi684-A (CW40197)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  564. CIRMi685-A (CW40198)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  565. CIRMi686-A (CW40199)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  566. CIRMi687-A (CW40200)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  567. CIRMi688-A (CW40201)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  568. CIRMi689-A (CW40206)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  569. CIRMi690-A (CW40207)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  570. CIRMi691-A (CW40208)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  571. CIRMi692-A (CW40209)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  572. CIRMi693-A (CW40211)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  573. CIRMi694-A (CW40212)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  574. CIRMi695-A (CW40213)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  575. CIRMi696-A (CW40214)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  576. CIRMi697-A (CW40217)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  577. CIRMi698-A (CW40218)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  578. CIRMi699-A (CW40219)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  579. CIRMi700-A (CW40220)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  580. CIRMi701-A (CW40221)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  581. CIRMi702-A (CW40222)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  582. CIRMi703-A (CW40224)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  583. CIRMi704-A (CW40225)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  584. CIRMi705-A (CW40226)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  585. CIRMi706-A (CW40227)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  586. CIRMi707-A (CW40228)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  587. CIRMi708-A (CW40229)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  588. CIRMi709-A (CW40230)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  589. CIRMi710-A (CW40231)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  590. CIRMi711-A (CW40232)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  591. CIRMi712-A (CW40233)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  592. CIRMi713-A (CW40234)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  593. CIRMi714-A (CW40235)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  594. CIRMi715-A (CW40236)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  595. CIRMi716-A (CW40237)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  596. CIRMi717-A (CW40239)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  597. CIRMi718-A (CW40243)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  598. CIRMi719-A (CW40244)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  599. CIRMi720-A (CW40245)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  600. CIRMi721-A (CW40246)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  601. CIRMi722-A (CW40247)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  602. CIRMi723-A (CW40249)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  603. CIRMi724-A (CW40250)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  604. CIRMi725-A (CW40251)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Idiopathic pulmonary fibrosis

  605. CIRMi736-A (CW30011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  606. CIRMi737-A (CW30012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  607. CIRMi762-A (CW30045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  608. CIRMi793-A (CW30080)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  609. CIRMi799-A (CW30086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  610. CIRMi817-A (CW30108)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  611. CIRMi836-A (CW30137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  612. CIRMi842-A (CW30143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  613. CIRMi846-A (CW30149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  614. CIRMi855-A (CW30161)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  615. CIRMi860-A (CW30167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  616. CIRMi861-A (CW30168)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  617. CIRMi862-A (CW30169)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  618. CIRMi863-A (CW30170)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  619. CIRMi864-A (CW30171)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  620. CIRMi865-A (CW30172)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  621. CIRMi892-A (CW30204)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  622. CIRMi893-A (CW30205)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  623. CIRMi908-A (CW30223)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  624. CIRMi909-A (CW30224)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  625. CIRMi910-A (CW30225)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Left ventricular non-compaction syndrome

  626. CIRMi911-A (CW30226)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  627. CIRMi912-A (CW30227)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  628. CIRMi913-A (CW30228)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  629. CIRMi914-A (CW30229)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  630. CIRMi915-A (CW30230)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  631. CIRMi916-A (CW30231)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  632. CIRMi917-A (CW30232)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  633. CIRMi918-A (CW30233)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  634. CIRMi919-A (CW30234)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  635. CIRMi920-A (CW30235)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  636. CIRMi921-A (CW30236)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  637. CIRMi922-A (CW30237)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  638. CIRMi923-A (CW30238)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  639. CIRMi924-A (CW30240)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  640. CIRMi925-A (CW30241)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  641. CIRMi926-A (CW30242)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  642. CIRMi927-A (CW30243)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  643. CIRMi928-A (CW30244)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  644. CIRMi929-A (CW30245)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  645. CIRMi930-A (CW30246)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  646. CIRMi931-A (CW30247)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  647. CIRMi932-A (CW30248)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  648. CIRMi933-A (CW30249)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  649. CIRMi934-A (CW30251)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  650. CIRMi935-A (CW30253)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  651. CIRMi936-A (CW30254)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  652. CIRMi937-A (CW30256)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  653. CIRMi938-A (CW30257)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  654. CIRMi939-A (CW30258)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  655. CIRMi940-A (CW30259)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  656. CIRMi941-A (CW30260)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  657. CIRMi942-A (CW30261)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  658. CIRMi943-A (CW30262)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  659. CIRMi944-A (CW30263)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  660. CIRMi945-A (CW30264)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  661. CIRMi947-A (CW30266)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  662. CIRMi956-A (CW30276)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  663. CIRMi969-A (CW30292)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  664. CIRMi970-A (CW30293)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  665. CIRMi971-A (CW30295)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  666. CIRMi972-A (CW30297)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Cardiomyopathy

  667. CIRMi973-A (CW30298)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  668. CIRMi974-A (CW30299)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  669. CIRMi976-A (CW30302)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  670. CIRMi983-A (CW30311)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  671. CIRMi993-A (CW30323)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  672. CIRMi00E-A (CW30335)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  673. CIRMi00K-A (CW30342)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  674. CIRMi01D-A (CW30364)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  675. CIRMi01H-A (CW30374)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  676. CIRMi02K-A (CW30417)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hypertrophic cardiomyopathy

  677. CIRMi02Q-A (CW30423)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  678. CIRMi02Z-A (CW30433)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Arrhythmogenic right ventricular dysplasia

  679. CIRMi03N-A (CW30447)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  680. CIRMi03T-A (CW30454)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  681. CIRMi04K-A (CW30473)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  682. CIRMi04U-A (CW30484)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Restrictive cardiomyopathy

  683. CIRMi05H-A (CW30500)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  684. CIRMi05N-A (CW30509)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Dilated cardiomyopathy

  685. CIRMi06C-A (CW10001)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  686. CIRMi06D-A (CW10002)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  687. CIRMi06E-A (CW10003)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  688. CIRMi06F-A (CW10004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  689. CIRMi06G-A (CW10005)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  690. CIRMi06H-A (CW10007)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  691. CIRMi06I-A (CW10009)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  692. CIRMi06J-A (CW10010)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  693. CIRMi06K-A (CW10011)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  694. CIRMi06L-A (CW10012)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  695. CIRMi06M-A (CW10013)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  696. CIRMi06N-A (CW10014)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  697. CIRMi06O-A (CW10015)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatic steatosis

  698. CIRMi06P-A (CW10018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  699. CIRMi06Q-A (CW10020)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  700. CIRMi06R-A (CW10021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  701. CIRMi06S-A (CW10023)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  702. CIRMi06T-A (CW10024)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  703. CIRMi06U-A (CW10025)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  704. CIRMi06V-A (CW10026)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  705. CIRMi06W-A (CW10027)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  706. CIRMi06X-A (CW10030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  707. CIRMi06Y-A (CW10033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  708. CIRMi06Z-A (CW10034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  709. CIRMi07A-A (CW10035)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  710. CIRMi07B-A (CW10036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  711. CIRMi07C-A (CW10037)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  712. CIRMi07D-A (CW10038)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  713. CIRMi07E-A (CW10039)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  714. CIRMi07F-A (CW10040)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  715. CIRMi07G-A (CW10041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  716. CIRMi07H-A (CW10042)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  717. CIRMi07I-A (CW10044)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  718. CIRMi07J-A (CW10045)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  719. CIRMi07K-A (CW10050)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  720. CIRMi07L-A (CW10054)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  721. CIRMi07M-A (CW10058)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  722. CIRMi07N-A (CW10060)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  723. CIRMi07O-A (CW10061)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  724. CIRMi07P-A (CW10062)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  725. CIRMi07Q-A (CW10063)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  726. CIRMi07R-A (CW10064)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  727. CIRMi07S-A (CW10066)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  728. CIRMi07T-A (CW10067)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  729. CIRMi07U-A (CW10068)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  730. CIRMi07V-A (CW10069)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  731. CIRMi07W-A (CW10073)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  732. CIRMi07X-A (CW10074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  733. CIRMi07Y-A (CW10075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  734. CIRMi07Z-A (CW10076)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  735. CIRMi08A-A (CW10077)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  736. CIRMi08B-A (CW10078)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  737. CIRMi08C-A (CW10079)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  738. CIRMi08D-A (CW10081)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  739. CIRMi08E-A (CW10083)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  740. CIRMi08F-A (CW10084)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  741. CIRMi08G-A (CW10085)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  742. CIRMi08H-A (CW10086)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  743. CIRMi08I-A (CW10087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  744. CIRMi08J-A (CW10088)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  745. CIRMi08K-A (CW10089)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  746. CIRMi08L-A (CW10090)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  747. CIRMi08M-A (CW10091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  748. CIRMi08N-A (CW10093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  749. CIRMi08O-A (CW10094)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  750. CIRMi08P-A (CW10095)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  751. CIRMi08Q-A (CW10096)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  752. CIRMi08R-A (CW10097)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  753. CIRMi08S-A (CW10098)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  754. CIRMi08T-A (CW10100)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  755. CIRMi08U-A (CW10101)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  756. CIRMi08V-A (CW10102)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  757. CIRMi08W-A (CW10103)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  758. CIRMi08X-A (CW10104)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  759. CIRMi08Y-A (CW10107)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  760. CIRMi08Z-A (CW10109)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  761. CIRMi09A-A (CW10110)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  762. CIRMi09B-A (CW10111)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  763. CIRMi09C-A (CW10114)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  764. CIRMi09D-A (CW10115)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  765. CIRMi09E-A (CW10116)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  766. CIRMi09F-A (CW10118)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  767. CIRMi09G-A (CW10120)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  768. CIRMi09H-A (CW10121)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  769. CIRMi09I-A (CW10122)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  770. CIRMi09J-A (CW10126)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  771. CIRMi09K-A (CW10127)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  772. CIRMi09L-A (CW10128)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  773. CIRMi09M-A (CW10130)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  774. CIRMi09N-A (CW10131)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  775. CIRMi09O-A (CW10133)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  776. CIRMi09P-A (CW10135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  777. CIRMi09Q-A (CW10136)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  778. CIRMi09R-A (CW10137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  779. CIRMi09S-A (CW10139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  780. CIRMi09T-A (CW10141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  781. CIRMi09U-A (CW10142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  782. CIRMi09V-A (CW10143)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  783. CIRMi09W-A (CW10144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  784. CIRMi09X-A (CW10146)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  785. CIRMi09Y-A (CW10147)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  786. CIRMi09Z-A (CW10148)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  787. CIRMi10A-A (CW10149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  788. CIRMi10B-A (CW10150)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  789. CIRMi10C-A (CW10152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  790. CIRMi10D-A (CW10153)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  791. CIRMi10E-A (CW10154)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  792. CIRMi10F-A (CW10155)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  793. CIRMi10G-A (CW10156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  794. CIRMi10H-A (CW10157)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  795. CIRMi10I-A (CW10158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  796. CIRMi10J-A (CW10159)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  797. CIRMi10K-A (CW10160)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  798. CIRMi10L-A (CW10162)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  799. CIRMi10M-A (CW10163)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  800. CIRMi10N-A (CW10165)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  801. CIRMi10O-A (CW10166)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  802. CIRMi10P-A (CW10167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  803. CIRMi10Q-A (CW10168)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  804. CIRMi10R-A (CW10169)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  805. CIRMi10S-A (CW10171)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  806. CIRMi10T-A (CW10172)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  807. CIRMi10U-A (CW10173)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  808. CIRMi10V-A (CW10175)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  809. CIRMi10W-A (CW10176)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  810. CIRMi10X-A (CW10177)

    United States California Institute for Regenerative Medicine (CIRM)

  811. CIRMi10Y-A (CW10178)

    United States California Institute for Regenerative Medicine (CIRM)

  812. CIRMi10Z-A (CW10181)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  813. CIRMi11A-A (CW10182)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  814. CIRMi11B-A (CW10183)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  815. CIRMi11C-A (CW10184)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatic steatosis

  816. CIRMi11D-A (CW10185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  817. CIRMi11E-A (CW10186)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  818. CIRMi11F-A (CW10187)

    United States California Institute for Regenerative Medicine (CIRM)

  819. CIRMi11G-A (CW10188)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  820. CIRMi11H-A (CW10189)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  821. CIRMi11I-A (CW10190)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  822. CIRMi11J-A (CW10191)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  823. CIRMi11K-A (CW10192)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  824. CIRMi11L-A (CW10201)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  825. CIRMi11M-A (CW10202)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  826. CIRMi11N-A (CW10203)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  827. CIRMi11O-A (CW10205)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Hepatitis c infection

  828. CIRMi11P-A (CW10206)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  829. CIRMi11Q-A (CW10208)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Metabolic dysfunction-associated steatohepatitis

  830. CIRMi11W-A (CW11004)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  831. CIRMi12E-A (CW11018)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  832. CIRMi12G-A (CW11030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Generalized anxiety disorder - 7 questionnaire

  833. CIRMi12H-A (CW11031)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  834. CIRMi12I-A (CW11032)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  835. CIRMi12J-A (CW11033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  836. CIRMi12K-A (CW11034)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  837. CIRMi12L-A (CW11036)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  838. CIRMi12N-A (CW11041)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  839. CIRMi12T-A (CW11075)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  840. CIRMi12Z-A (CW11093)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  841. CIRMi13R-A (CW11140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Unipolar depression

  842. CIRMi14G-A (CW20021)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  843. CIRMi14M-A (CW20030)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  844. CIRMi14P-A (CW20033)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  845. CIRMi15S-A (CW20074)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  846. CIRMi16D-A (CW20087)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  847. CIRMi16F-A (CW20091)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  848. CIRMi17L-A (CW20135)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  849. CIRMi17N-A (CW20137)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  850. CIRMi17O-A (CW20139)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  851. CIRMi17P-A (CW20140)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  852. CIRMi17Q-A (CW20141)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  853. CIRMi17R-A (CW20142)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  854. CIRMi17S-A (CW20144)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  855. CIRMi17T-A (CW20146)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  856. CIRMi17U-A (CW20149)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  857. CIRMi17V-A (CW20150)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  858. CIRMi17W-A (CW20151)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  859. CIRMi17X-A (CW20152)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  860. CIRMi17Y-A (CW20153)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  861. CIRMi17Z-A (CW20156)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  862. CIRMi18A-A (CW20158)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  863. CIRMi18B-A (CW20164)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  864. CIRMi18C-A (CW20166)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  865. CIRMi18D-A (CW20167)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  866. CIRMi18E-A (CW20170)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  867. CIRMi18F-A (CW20178)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  868. CIRMi18G-A (CW20179)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  869. CIRMi18H-A (CW20181)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  870. CIRMi18I-A (CW20183)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  871. CIRMi18J-A (CW20184)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  872. CIRMi18K-A (CW20185)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  873. CIRMi18L-A (CW20186)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  874. CIRMi18M-A (CW20188)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  875. CIRMi18N-A (CW20192)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  876. CIRMi18O-A (CW20193)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  877. CIRMi18P-A (CW20195)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  878. CIRMi18Q-A (CW20196)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  879. CIRMi18R-A (CW20200)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  880. CIRMi18S-A (CW20201)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  881. CIRMi18T-A (CW20202)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  882. CIRMi18U-A (CW20203)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  883. CIRMi18V-A (CW20204)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  884. CIRMi18W-A (CW20206)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  885. CIRMi18X-A (CW20207)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  886. CIRMi18Y-A (CW20209)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  887. CIRMi18Z-A (CW20210)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  888. CIRMi19A-A (CW20212)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  889. CIRMi19B-A (CW20213)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  890. CIRMi19C-A (CW20214)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  891. CIRMi19D-A (CW20222)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  892. CIRMi19E-A (CW20225)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  893. CIRMi19F-A (CW20226)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

  894. CIRMi19P-A (CW20252)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Normal (average)

  895. CIRMi20D-A (CW20323)

    United States California Institute for Regenerative Medicine (CIRM)
    Disease:

    Autism spectrum disorder

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

    South Korea Catholic University of Korea (CMC)
    Disease:

    Karyomegalic interstitial nephritis

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

    South Korea Catholic University of Korea (CMC)
    Disease:

    Gitelman syndrome

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

    South Korea Catholic University of Korea (CMC)
    Disease:

    Fabry disease

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

    South Korea Catholic University of Korea (CMC)
    Disease:

    Birt-hogg-dube syndrome

  900. CMDi001-A (01016)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  901. CMDi002-A (01173)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  902. CMDi004-A (01175)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  903. CMDi005-A (01176)

    United States CureCMD (CMD)
    Disease:

    Congenital muscular dystrophy

  904. CMFTe001-A (Man-2)

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

  905. CMGANTi003-A (SEMD1)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  906. CMGANTi004-A (SEMD2)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    X-linked spondyloepimetaphyseal dysplasia

  907. CMGANTi005-A (iPSC_MFS_FBN1_MCE-KB_C8)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Marfan syndrome

  908. CMGANTi008-A (iPSC_MFS_FBN1_Fi930129_C8)

    Belgium Center of Medical Genetics Antwerp (CMGANT)
    Disease:

    Marfan syndrome

  909. CPGHi004-A

    China Chinese PLA General Hospital (CPGH)
    Disease:

    Normal (average)

  910. CRICKi001-A (iFCI001)

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

    Intellectual disability

  911. CRICKi002-A (iFCI027)

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

    Intellectual disability

  912. CRICKi007-A (iFCI009)

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

    Spinal muscular atrophy with lower extremity predominant

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

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

    X-linked centronuclear myopathy

  914. CRICKi011-A (iFCI016)

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

    Young-onset parkinson disease

  915. CRICKi012-A (iFCI017)

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

    Young-onset parkinson disease

  916. CRICKi013-A (iFCI018 Clone 6)

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

    Von hippel-lindau disease tumor suppressor

  917. CRICKi015-A (iFCI020 Clone 1)

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

    Von hippel-lindau disease tumor suppressor

  918. CRICKi016-A (iFCI021 Clone 7)

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

    Lung cancer

  919. CRICKi020-A (iFCI025 and iKER 10)

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

    Normal (average)

  920. CRICKi021-A (iFCI007)

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

    Ullrich congenital muscular dystrophy

  921. CRICKi022-A (iFCI031)

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

    Lung cancer

  922. CRICKi024-A (XXY-A4)

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

    Obsolete_klinefelter's syndrome

  923. CRICKi024-C (XXY-3A9)

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

    Obsolete_klinefelter's syndrome

  924. CRICKi024-E (2A6 C11)

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

    Obsolete_klinefelter's syndrome

  925. CRICKi024-I-1 (3A43_XO)

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

    Obsolete_klinefelter's syndrome

  926. CRICKi025-A (iFCI033 CL7)

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

    Normal (average)

  927. CRICKi026-A (iFCI035 CL1)

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

    Normal (average)

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

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

    Normal (average)

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

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

    Normal (average)

  930. CRTDi003-A (CRTD2)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  931. CRTDi004-A (CRTD1)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  932. CRTDi005-B (CRTD5)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  933. CRTDi008-B

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Aicardi-goutieres syndrome 5

  934. CRTDi011-B (IDP52555 #13)

    Germany Center for Regenerative Therapies Dresden (CRTD)
    Disease:

    Normal (average)

  935. CSBZZUi002-A

    China The first affiliated Hospital of Zhengzhou University (CSBZZU)
    Disease:

    Normal (average)

  936. CSBZZUi003-A

    China The first affiliated Hospital of Zhengzhou University (CSBZZU)
    Disease:

    Normal (average)

  937. CSCIi002-A (niPSC HDF75 and niPSC-75.1c2)

    United Kingdom Wellcome Trust - MRC Stem Cell Institute (CSCI)
    Disease:

    Normal (average)

  938. CSIRi001-A (CSIR-SA-001-J4)

    South Africa Council for Scientific and Industrial Research South Africa (CSIR)
    Disease:

    Normal (average)

  939. CSIRi001-B (CSIR-SA-001-J3)

    South Africa Council for Scientific and Industrial Research South Africa (CSIR)
    Disease:

    Normal (average)

  940. CSMCi001-A-2 (2. CS011MEN1-n4.Corrected1)

    United States Cedars Sinai Medical Center, (CSMC)
    Disease:

    Multiple endocrine neoplasia type 1

  941. CSSi013-A

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

    Normal (average)

  942. CSSi014-A

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

    Mucopolysaccharidosis ii

  943. CSSi023-A

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

    Autosomal dominant optic atrophy

  944. CSUe005-A (chHES-22)

    China Central South University (CSU)

  945. CSUASOi013-A

    China Aier School of Ophthalmology (CSUASO)
    Disease:

    Retinitis pigmentosa

  946. CSUXHEi001-A

    China Central South University (CSUXHE)
    Disease:

    Normal (average)

  947. CUIMCi004-B

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

    Class 3 obesity

  948. CVTTHi001-A

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

    Activated pi3k-delta syndrome

  949. CVTTHi001-A-1

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

    Activated pi3k-delta syndrome

  950. CVTTHi002-A

    Spain Centro Vasco de Transfusión y Tejidos Humanos (CVTTH)

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

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

    Normal (average)

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

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

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

    Parkinson disease

  956. DHMi001-A (Control_S)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  957. DHMi002-A (HLHS_606)

    Germany German Heart Center Munich (DHM)
    Disease:

    Hypoplastic left heart syndrome

  958. DHMi003-A (HLHS_612)

    Germany German Heart Center Munich (DHM)
    Disease:

    Hypoplastic left heart syndrome

  959. DHMi004-A (HOS_1460)

    Germany German Heart Center Munich (DHM)
    Disease:

    Holt-oram syndrome

  960. DHMi005-A (Control_L)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

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

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  962. DHMi005-A-9 (L Delta B2M Clone 11)

    Germany German Heart Center Munich (DHM)
    Disease:

    Normal (average)

  963. DHMCi010-A (Neph021C)

    Germany Dietmar Hopp Metabolic Center (DHMC)
    Disease:

    Congenital nephrotic syndrome, finnish type

  964. DHMCi019-A (Neph018C)

    Germany Dietmar Hopp Metabolic Center (DHMC)
    Disease:

    Familial nephrotic syndrome

  965. DMBi007-A

    Poland Department of Medical Biotechnology (DMB)
    Disease:

    Psoriasis

  966. DMSCi001-A

    Thailand Department of Medical Sciences (DMSC)
    Disease:

    Normal (average)

  967. DMSCi002-A

    Thailand Department of Medical Sciences (DMSC)
    Disease:

    Normal (average)

  968. DPNJMUi002-A

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

    Progressive familial intrahepatic cholestasis type 3

  969. DRICUi002-A (ADANG10242CA)

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

    Late-onset alzheimer's disease

  970. DRICUi003-A (LC56A10005A)

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

    Late-onset alzheimer's disease

  971. DRICUi004-A (LC56A10012A)

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

    Late-onset alzheimer's disease

  972. DRICUi006-A (ADANG10496CA)

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

    Late-onset alzheimer's disease

  973. DRICUi007-A (ADANG10605CA)

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

    Late-onset alzheimer's disease

  974. DRICUi010-A (BS38A10004A)

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

    Late-onset alzheimer's disease

  975. DRICUi011-A (BS38A10002A)

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

    Late-onset alzheimer's disease

  976. DRICUi013-A (SC45A10021A)

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

    Late-onset alzheimer's disease

  977. DRICUi016-A (GU66A10008a)

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

    Late-onset alzheimer's disease

  978. DRICUi017-A (FB12A10007a)

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

    Late-onset alzheimer's disease

  979. DRICUi018-A (BH09A10003A)

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

    Late-onset alzheimer's disease

  980. DRICUi019-A (NE37A10024a)

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

    Late-onset alzheimer's disease

  981. DRICUi022-A (CF00C90161A)

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

    Normal (average)

  982. DRICUi023-A (NF35A00021A)

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

    Late-onset alzheimer's disease

  983. DRICUi026-A (ADCAR24745UC)

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

    Normal (average)

  984. DRICUi027-A (ADCAR20186CA)

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

    Late-onset alzheimer's disease

  985. DRICUi028-A (NE37A10025A)

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

    Late-onset alzheimer's disease

  986. DRICUi029-A (MW14A10014A)

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

    Late-onset alzheimer's disease

  987. DRICUi030-A (CF00C90028A)

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

    Normal (average)

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

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

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

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

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

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

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

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

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

    United States University of Edinburgh (ED)
    Disease:

    Parkinson disease

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

    United Kingdom University of Edinburgh (ED)
    Disease:

    Parkinson disease

  994. EDi011-C (RCi141)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  995. EDi012-A (RCi163)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  996. EDi012-B (RCi164)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  997. EDi012-C (RCi165)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  998. EDi013-A (RCi192)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  999. EDi013-B (RCi193)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  1000. EDi013-C (RCi214)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  1001. EDi014-A (RCi175)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Obsolete_unipolar depression

    Disease:

    Anti-social behavior

  1002. EDi017-A (RCi174)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  1003. EDi017-B (RCi181)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  1004. EDi018-B (RCi212)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Bipolar disorder

  1005. EDi019-A (RCi166)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  1006. EDi021-A (CS0395iCTR-LBCn3)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  1007. EDi022-A (CS0617iCTR-LBCn1)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  1008. EDi023-A (CS0791iCTR-LBCn1)

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  1009. EDi024-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1010. EDi025-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1011. EDi027-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1012. EDi028-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1013. EDi029-A

    United Kingdom University of Edinburgh (ED)
    Disease:

    Normal (average)

  1014. EDi031-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1015. EDi034-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1016. EDi035-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1017. EDi036-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1018. EDi038-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1019. EDi040-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1020. EDi043-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1021. EDi044-A

    United States University of Edinburgh (ED)
    Disease:

    Normal (average)

  1022. EDe006-A (RH 7)

    United Kingdom University of Edinburgh (ED)

  1023. EHTJUi002-A (DF-GMP-ZB11AR-H)

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

    Normal (average)

  1024. EMCi169-B (Clone_3)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  1025. EMCi169-C (Clone_9)

    Netherlands Erasmus MC (EMC)
    Disease:

    Tuberous sclerosis complex

  1026. EMCi225-D (Clone_8)

    Netherlands Erasmus MC (EMC)
    Disease:

    Obsolete_neurodevelopmental disorder

  1027. ERPLi004-A (A1AT iPSC C1)

    India Eyestem Research Private Limited (ERPL)
    Disease:

    Alpha 1-antitrypsin deficiency

  1028. ESi002-A (SP08#1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  1029. ESi005-A (cFA404-KiPS4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Fanconi anemia

  1030. ESi005-B (cFA404-KiPS4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Fanconi anemia

  1031. ESi006-A (SP13#4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Parkinson disease

  1032. ESi007-A (CBiPS1sv-4F-40)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1033. ESi008-B (KiPS3F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1034. ESi028-A (KiPS4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1035. ESi038-B (CBiPS32-3F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1036. ESi040-A ([PD] FiPS006-4F-11)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_parkinson's disease

  1037. ESi043-A ([ctrl.PD] FiPS005-4F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1038. ESi044-A (FiPS Ctrl1-mR5F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1039. ESi044-D (FiPS Ctrl1-R4F-4)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1040. ESi045-B (FiPS Ctrl2-Ep6F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1041. ESi052-A (MS FiPS 5-R4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Multiple sclerosis

  1042. ESi057-A ([DUP7] FiPS-4F-3-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  1043. ESi058-A ([DUP7] FiPS-4F-4-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  1044. ESi060-A ([SWB] FiPS-4F-5-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  1045. ESi065-A ([IDDM1] FiPS 1.13-Ep6F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_type i diabetes mellitus

  1046. ESi069-A (SWB FiPS 344-R4F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams-beuren syndrome

  1047. ESi071-A (DUPSW FiPS 701-R4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Autism

  1048. ESi072-A (OCD FiPS 1-EP6F-16)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_obsessive-compulsive disorder

  1049. ESi073-A (OCD FiPS 2-EP6F-10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Obsolete_obsessive-compulsive disorder

  1050. ESi074-A (CT PBiPS1-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiotoxicity

  1051. ESi077-A (CABi001-A and PRPF31-MiPS4F3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Retinitis pigmentosa

  1052. ESi078-A (cPRPF31-MiPS4F7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1053. ESi079-A (cAMDdh09-MiPS4F17)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1054. ESi085-A (cAMDdh01-MiPS4F8 and DH01 c8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1055. ESi087-A (BT1-UCiPS4F1 and BT-iPSCs 1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Low grade glioma

  1056. ESi088-A (BT2-UCiPS4F1 and BT-iPSCs 2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Brain cancer

  1057. ESi090-A (Ctrl2-UCiPS4F1 and nonT-iPSCs 2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cryptorchidism

  1058. ESi091-A (HLA91-MiPS4F3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1059. ESi094-A (Hz 1-8-3 CBiPS4 Sv4F F6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1060. ESi095-A (Hz 3-7-15 CBiPS3- Sv4F E9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1061. ESi099-A (Hz 33-14-1 CBiPS6-Sv4F H6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1062. ESi100-A (NW FiPS 10II.3-R4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Williams syndrome

  1063. ESi104-A (PMM2-CDG FiPS48-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Pmm2-cdg

  1064. ESi106-A (MD FiPS3304-Sv4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Mitochondrial disease

  1065. ESi107-A (TAC PBiPS1-Sv4F-3 and ATTR-CM PBiPS1-Sv4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  1066. ESi110-A (HLA89-MiPS4F8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1067. ESi111-A (Ctrl EiPS J9 mR6F-8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1068. ESi112-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1069. ESi114-A

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1070. ESi118-A (MD FiPS3236-Sv4F-9)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Mitochondrial disease

  1071. ESi120-A (RRMS PBiPS11-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  1072. ESi121-A (RRMS PBiPS12-Sv4F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  1073. ESi122-A (PPMS PBiPS7-Sv4F-5)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  1074. ESi123-A (PPMS PBiPS8-Sv4F-13)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  1075. ESi124-A (PPMS PBiPS9-Sv4F-12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  1076. ESi128-A (PPMS PBiPS10-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Primary progressive multiple sclerosis

  1077. ESi129-A (RRMS PBiPS13-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  1078. ESi130-A (RRMS PBiPS14-Sv4F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Relapsing-remitting multiple sclerosis

  1079. ESi133-A (CT PBiPS2-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Chemically induced cardiotoxicity

  1080. ESi136-A (NDD PBiPS1-Sv4F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Neurodevelopmental disorders

  1081. ESi139-A (ATTR CM PBiPS4-Sv4F-13)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Cardiac attr amyloidosis

  1082. ESi140-A (CT PBiPS3-Sv4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Chemically induced cardiotoxicity

  1083. ESi146-A (NEDCASB FiPS319-Ep6F-7)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities

  1084. ESi147-A (HLD18 FiPS4379-Ep6F-2)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Leukodystrophy, hypomyelinating, 18

  1085. ESi149-A (GNB1 FiPS1-Ep6F-1)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Encephalopathy

  1086. ESi150-A (GNB1 FiPS2-Ep6F-6)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Encephalopathy

  1087. ESi152-A (GNB1 FiPS4-Ep6F-12)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Encephalopathy

  1088. ESi155-A (PMM2 CDG FiPS01-Sv4F-11)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Pmm2-cdg

  1089. ESi156-A (ALD FiPS1-Ep6F-11)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Adrenoleukodystrophy

  1090. ESi157-A (STGD90-MiPS4F10)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Stargardt disease

  1091. ESi158-A (STGD73-MiPS4F8)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Stargardt disease

  1092. ESi159-A (ALD FiPS2-Ep6F-11)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Adrenoleukodystrophy

  1093. ESi162-A (WFS1 FiPS 34-Ep6F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Wolfram syndrome

  1094. ESi162-B (WFS1 FiPS 34-Ep6F-13)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Wolfram syndrome

  1095. ESi168-A (S PBiPS 1580-Sv4F-3)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Schizophrenia

  1096. ESe009-A (ES-2)

    Spain Spanish Stem Cell Bank (ES)

  1097. ESe013-A (VAL-5)

    Spain Spanish Stem Cell Bank (ES)

  1098. ESe014-A (ES-4 and ES[4])

    Spain Spanish Stem Cell Bank (ES)

  1099. ESe015-A (ES-6)

    Spain Spanish Stem Cell Bank (ES)

  1100. ESe026-A (ES-11EM)

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Hereditary multiple exostoses

  1101. ESe028-A (bES[13])

    Spain Spanish Stem Cell Bank (ES)
    Disease:

    Normal (average)

  1102. ESIBIe005-A (HES-5)

    Singapore ES Cell International Pte Ltd. (ESIBI)

  1103. EUSOMi001-A (3-1 and LQTS003-1)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Long qt syndrome 2

  1104. EUSOMi005-A (LQTS005-1, 5-1)

    United States Emory University School of Medicine (EUSOM)
    Disease:

    Long qt syndrome 1

  1105. WAe009-A-43

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

    Long qt syndrome

  1106. WAe001-A-72 (H1-FTO-Knockout-13)

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

    Normal (average)

  1107. FAMRCi001-A (ARVC2)

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

    Inherited arrhythmogenic cardiomyopathy

  1108. FAMRCi001-B (ARVC4)

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

    Inherited arrhythmogenic cardiomyopathy

  1109. FAMRCi002-A (OBC7)

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

    Desminopathy

  1110. FAMRCi003-A (108-1)

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

    Normal (average)

  1111. FAMRCi003-B (108-2)

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

    Normal (average)

  1112. FAMRCi004-A (DSPL1)

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

    Sick sinus syndrome

    Disease:

    Atrioventricular block

    Disease:

    Hereditary progressive cardiac conduction defect

  1113. FAMRCi004-B (DSPL10)

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

    Sick sinus syndrome

    Disease:

    Atrioventricular block

    Disease:

    Hereditary progressive cardiac conduction defect

  1114. FAMRCi005-A (LMNA B4)

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

    Paroxysmal ventricular tachycardia

    Disease:

    Atrioventricular block

    Disease:

    Obsolete_myopathy

  1115. FAMRCi005-B (LMNA B5)

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

    Paroxysmal ventricular tachycardia

    Disease:

    Atrioventricular block

    Disease:

    Obsolete_myopathy

  1116. FAMRCi006-A (LMNA T3)

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

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  1117. FAMRCi006-B (LMNA T4)

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

    Emery-dreifuss muscular dystrophy

    Disease:

    Dilated cardiomyopathy

  1118. FAMRCi007-A (LMNA #23)

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

    Emery-dreifuss muscular dystrophy

    Disease:

    Atrioventricular block

    Disease:

    Paroxysmal atrial fibrillation

  1119. FAMRCi007-B (LMNA #19)

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

    Emery-dreifuss muscular dystrophy

    Disease:

    Atrioventricular block

    Disease:

    Paroxysmal atrial fibrillation

  1120. FAMRCi008-A (10X-12)

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

    Normal (average)

  1121. FAMRCi009-A (RCMP43)

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

    Restrictive cardiomyopathy

  1122. FAMRCi010-A (RCMP48)

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

    Restrictive cardiomyopathy

  1123. FAMRCi011-A (ARVC51)

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

    Inherited arrhythmogenic cardiomyopathy

  1124. FAMRCi011-B (ARVC51b)

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

    Inherited arrhythmogenic cardiomyopathy

  1125. FAMRCi012-A (Brug/VT-83)

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

    Ventricular fibrillation

  1126. FAMRCi013-A (ARVC300-14)

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

    Arrhythmogenic right ventricular cardiomyopathy

  1127. FAMRCi013-B (ARVC300-21)

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

    Arrhythmogenic right ventricular cardiomyopathy

  1128. FAMRCi013-C (ARVC300-25)

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

    Arrhythmogenic right ventricular cardiomyopathy

  1129. FAMRCi016-A (RCMP41-2)

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

    Restrictive cardiomyopathy

  1130. FCBRNi001-A

    Russia Federal Center of Brain Research and Neurotechnologies (FCBRN)
    Disease:

    Normal (average)

  1131. FDCHDPi001-A (FDCHDP01)

    China Fudan University (FDCHDP)
    Disease:

    Tourette syndrome

  1132. FDHPIi001-A

    China (WITHDRAWN) Fudan University (FDHPI)
    Disease:

    Neurodegeneration

  1133. FDIBSi001-A (iPSCx-x-ADNP-F)

    China Institutes of Brain Science,Fudan University (FDIBS)
    Disease:

    Adnp-related multiple congenital anomalies - intellectual disability - autism spectrum disorder

  1134. FDIBSi002-A (iPSCx-x-DYRK1A-G/A)

    China Institutes of Brain Science,Fudan University (FDIBS)
    Disease:

    Intellectual developmental disorder, autosomal dominant 7

  1135. 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

  1136. FINi001-A (FI.SPSM.SCN2A.R1882Q.009)

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

    Developmental and epileptic encephalopathy

  1137. FINCBi005-A (mt1072 clone #103 and mt1072 #103)

    Italy Fondazione IRCCS Istituto Neurologico C. Besta (FINCB)
    Disease:

    Leber hereditary optic neuropathy

  1138. FJMUUHi001-A

    China Fujian Medical University Union Hospital (FJMUUH)
    Disease:

    Parkinson's disease 7

  1139. FLENIi004-A (FBAD1)

    Argentina Fundación para la Lucha contra las Enfermedades Neurológicas de la Infancia (FLENI)
    Disease:

    Familial alzheimer disease

  1140. FMCPGHi001-A (301-iPSC-normal-001A)

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

    Normal (average)

  1141. FMCPGHi002-A (301-iPSC-normal-002B)

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

    Normal (average)

  1142. FMCPGHi003-A (301-iPSC-FHM-001A)

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

    Familial hemiplegic migraine 3

  1143. FMCPGHi006-A

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

    Duchenne muscular dystrophy

  1144. FMMUNIi001-A (I-WT)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Normal (average)

  1145. FMMUNIi002-A (I-IF)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Ventricular fibrillation

  1146. FMMUNIi003-A (I-CPVT)

    Czech Republic Faculty of Medicine, Masaryk University (FMMUNI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  1147. 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

  1148. FRIMOi002-A (RP2_FiPS4F2.2)

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

    Retinitis pigmentosa

  1149. FRIMOi003-A (STGD1_ FiPS4F1.5)

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

    Stargardt disease

  1150. FRIMOi004-A (STGD2_ FiPS4F1.7)

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

    Stargardt disease

  1151. FRIMOi005-A (RP3_FiPS4F11)

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

    Retinitis pigmentosa

  1152. FRIMOi006-A (BEST1_FiPS4F1)

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

    Bestrophinopathy

  1153. FRIMOi007-A (PDE6C_FiPS4F1)

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

    Achromatopsia

  1154. FUHSi001-A

    China Huashan Hospital of Fudan University (FUHS)
    Disease:

    Obsolete_cervical artery dissection

  1155. GEMi002-A (GN-IPS-14-2)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  1156. GEMi004-A (GN-IPS-135-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  1157. GEMi005-A (GN-IPS-160-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  1158. GEMi006-A (GN-IPS-201-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  1159. GEMi009-A (GN-IPS-204-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  1160. GEMi013-A (GN-IPS-208-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  1161. GEMi016-A (GN-IPS-211-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  1162. GEMi020-A (GN-IPS-215-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  1163. GEMi023-A (GN-IPS-218-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  1164. GEMi025-A (GN-IPS-220-1)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  1165. GEMi026-A (GN-IPS-46-3)

    China Shanghai Gemple Biotech Co.,Ltd (GEM)
    Disease:

    Normal (average)

  1166. GENEAe008-A (GENEA009 and SIVF09)

    Australia Genea (GENEA)

  1167. GENEAe013-A (GENEA089)

    Australia Genea (GENEA)
    Disease:

    Huntington disease

  1168. GENEAe014-A (GENEA029)

    United States Genea (GENEA)
    Disease:

    Normal (average)

  1169. GENEAe015-A (GENEA020)

    United States Genea (GENEA)
    Disease:

    Huntington disease

  1170. GENEAe016-A (GENEA022)

    Australia Genea (GENEA)
    Disease:

    Normal (average)

  1171. GENEAe017-A (GENEA023)

    Australia Genea (GENEA)
    Disease:

    Normal (average)

  1172. GENEAe020-A (GENEA019)

    Australia Genea (GENEA)
    Disease:

    Normal (average)

  1173. GENEAe021-A (GENEA021)

    Australia Genea (GENEA)
    Disease:

    Normal (average)

  1174. GENYOi004-A (ASD-PBMC-iPS4F2)

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

    Adnp syndrome

  1175. WAe009-A-7 (H9-mHOXA9)

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

    Normal (average)

  1176. WAe001-A-76 (H1-RNF1-/-)

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

    Parkinson disease

  1177. WAe009-A-84

    China Guangxi Institute of Cardiovascular Diseases (GICD)
    Disease:

    Congenital heart disease

  1178. GWCMCi006-A (GWCMCi-GRIN1)

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

    Obsolete_neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant

  1179. GZHMCi011-A (SCA3-LXM)

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

    Normal (average)

  1180. WAe001-A-3S (H1-FCGR3A-EGFP)

    China Guangzhou Laboratory (GZL)
    Disease:

    Normal (average)

  1181. HADe003-A (HAD 3)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Factor viii deficiency

  1182. HADe004-A (HAD 4)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Familial dysautonomia

  1183. HADe007-A (HAD-C 100)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal (average)

  1184. HADe008-A (HAD-C 102)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal (average)

  1185. HADe009-B (HAD-C 106 Single-cell, Feeder-free (Seed Cell Bank, SCB))

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal (average)

  1186. HADe011-A (HAD-C 104 cGMP-grade, xeno-free Single-cell, Feeder-free Master Cell Bank)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal (average)

  1187. HADe012-A (HAD-C 105 cGMP-grade, xeno-free Single-cell, Feeder-free Master Cell Bank)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal (average)

  1188. HADe013-A (HAD-C 107 cGMP-grade, xeno-free Single-cell, Feeder-free Master Cell Bank)

    Israel Hadassah University Hospital (HAD)
    Disease:

    Normal (average)

  1189. HCORDi001-C (M2_IPSC3_C)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  1190. HCORDi001-F (M2_IPSC3_M)

    Brazil Hemocord Clínica Médica Ltda (HCORD)
    Disease:

    Normal (average)

  1191. HEBHMUi010-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Normal (average)

  1192. HEBHMUi013-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Alzheimer's disease

  1193. HEBHMUi018-A

    China Hebei Medical University (HEBHMU)
    Disease:

    Baraitser-winter syndrome 1

  1194. HHUUKDi001-A (ISRM-UM51 and UM51-iPSC)

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

    Normal (average)

  1195. HHUUKDi009-A (TFBJ)

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

    Normal (average)

  1196. HHUUKDi011-A (AATD iPSC-1 and ISRM-AATD-iPSC-1)

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

    Alpha-1 antitrypsin deficiency

  1197. HHUUKDi013-A (ISRM-AATD-iPSC-3)

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

    Alpha-1 antitrypsin deficiency

  1198. HIMRi003-A (p.A46T CAV3 hiPSCs #2)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Caveolinopathy

  1199. HIMRi006-A (GAA c.307T>G hiPSC)

    Germany Heimer Institute for Muscle Research (HIMR)
    Disease:

    Glycogen storage disease due to acid maltase deficiency, infantile onset

  1200. HKUi002-A (AYC12 and HKUi002-A-AYC12)

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

    Dilated cardiomyopathy

  1201. HMGUi001-A (XM001 and BIHi043-A)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Normal (average)

  1202. HMGUi001-A-1 (hINS-T2A-H2B-Cherry (+/-) and HMGUi001-A-1)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Normal (average)

  1203. HMGUi002-A (XM002)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Normal (average)

  1204. HMGUi004-A

    Germany Helmholtz Zentrum München (HMGU)

  1205. HMGUi006-A (152350)

    Germany Helmholtz Zentrum München (HMGU)
    Disease:

    Neurodegeneration with brain iron accumulation 5

  1206. HMSCATi001-A

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

    Normal (average)

  1207. HMSCATi003-A (PJW)

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

    Parkinson disease

  1208. HMSCATi005-A (LQH)

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

    Alzheimer's disease

  1209. HMSCATi007-A (GXM)

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

    Epilepsy, familial focal, with variable foci 1

  1210. HMSCATi008-A (TSC1-PL)

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

    Tuberous sclerosis

    Disease:

    Epilepsy

  1211. HMSCATi009-A (WZX)

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

    Frontotemporal dementia

  1212. HNMUi003-A (iPS-UC1290)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  1213. HNMUi009-A (iPS-UC1171)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  1214. HNMUi010-A (iPS-AF091)

    China Hainan Medical University (HNMU)
    Disease:

    Obsolete_thalassemia

  1215. HPCHi002-A

    China Henan Provincial Chest Hospital (HPCH)
    Disease:

    Dilated cardiomyopathy

  1216. HPIi006-A (RYR1-3278-R2A)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  1217. HPIi008-A (RYR1-4833-R7)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  1218. HPIi009-A (RYR1-15377-R1B)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Central core disease

  1219. HPIi010-A (MYH7-17773-R4A)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Myh7-related skeletal myopathy

  1220. HPIi011-A (MYH7-18681-R1A)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Myh7-related skeletal myopathy

  1221. HPIi012-A (MYH7-19203-R1D)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Myh7-related skeletal myopathy

  1222. HPIi013-A (OPDM_ABCD3)

    Australia Harry Perkins Institute of Medical Research (HPI)
    Disease:

    Oculopharyngodistal myopathy

  1223. HUJIi005-B (ID-iPS10)

    Israel Hebrew University of Jerusalem (HUJI)

  1224. HVRDe009-A (HuES9)

    United States Harvard University (HVRD)
    Disease:

    Normal (average)

  1225. HVRDe012-A (HuES12)

    United States Harvard University (HVRD)

  1226. HVRDe013-A (HuES13)

    United States Harvard University (HVRD)

  1227. HVRDe017-A (HuES17)

    United States Harvard University (HVRD)

  1228. HZSMHCi001-A

    China Hangzhou Seventh People’s Hospital Mental Health Center, Zhejiang University School of Medicine (HZSMHC)
    Disease:

    Bipolar disorder

  1229. HZSMHCi004-A

    China Hangzhou Seventh People’s Hospital Mental Health Center, Zhejiang University School of Medicine (HZSMHC)
    Disease:

    Major depressive disorder

  1230. IAIi001-A (IAIi001RSTS2-65-A)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Rubinstein-taybi syndrome

  1231. IAIi005-A (AC52)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Normal (average)

  1232. IAIi010-A (Kif5A 1847 C3)

    Italy Istituto Auxologico Italiano IRCCS (IAI)
    Disease:

    Autosomal dominant spastic paraplegia type 10

  1233. IBBISTi004-A (AS-GB clone 12)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Angelman syndrome

  1234. IBBISTi013-A (4_H22)

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Hypertrophic cardiomyopathy

  1235. IBBISTi016-A (Ctrl-MD2 (clone 7))

    Portugal Simão José Teixeira da Rocha (IBBIST)
    Disease:

    Normal (average)

  1236. IBPi001-A (HPrF iPSCs 20A)

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

    Normal (average)

  1237. ICANi001-A (CDGEN1.16)

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

    Obsolete_hypertrophic cardiomyopathy

  1238. ICANi002-A-3 (ICAN-BAG3-V468MC34)

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

    Dilated cardiomyopathy 1hh

  1239. ICANi002-A-4 (ICAN_BAG3_M468MC19)

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

    Dilated cardiomyopathy 1hh

  1240. ICANi002-A-5 (ICAN-PKP2-H695-W11)

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

    Arrhythmogenic right ventricular dysplasia 9

  1241. ICGi002-A (DMD1_1)

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

    Duchenne muscular dystrophy

  1242. ICGi002-B (DMD1_4)

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

    Duchenne muscular dystrophy

  1243. ICGi002-C (DMD1_11)

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

    Duchenne muscular dystrophy

  1244. ICGi003-A (f3SMA3)

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

    Spinal muscular atrophy type 3

  1245. ICGi005-A (iSMA40)

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

    Proximal spinal muscular atrophy type 1

  1246. ICGi006-A (m3SMA13)

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

    Proximal spinal muscular atrophy type 2

  1247. ICGi006-B (m3SMA20)

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

    Proximal spinal muscular atrophy type 2

  1248. ICGi007-A (47Q-3Lf)

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

    Huntington disease

  1249. ICGi008-A (m55Alz-9L)

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

    Obsolete_alzheimer's disease

  1250. ICGi013-A (iTAF13-26 and iTAF13del26)

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

    Intellectual disability

  1251. ICGi013-B (iTAF13del27 and iTAF13-27)

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

    Intellectual disability

  1252. ICGi014-A (2M_iALS)

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

    Obsolete_amyotrophic lateral sclerosis

  1253. ICGi015-A

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

    Parkinson disease

  1254. ICGi015-B

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

    Parkinson disease

  1255. ICGi015-B-1 (m6.7pCyto-17)

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

    Parkinson disease

  1256. ICGi017-A (TAF14dup10)

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

    Normal (average)

  1257. ICGi018-A (iHD38Q-3)

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

    Huntington's disease

  1258. ICGi018-B (iHD38Q-2)

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

    Huntington's disease

  1259. ICGi018-C (iHD38Q-1)

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

    Huntington's disease

  1260. ICGi019-A (HCM1f6)

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

    Hypertrophic cardiomyopathy

  1261. ICGi020-A (ATP7bIL23f)

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

    Wilson disease

  1262. ICGi020-B (ATP7bIL24f)

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

    Wilson disease

  1263. ICGi021-A (K6-4f)

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

    Normal (average)

  1264. ICGi021-A-1 (K6-4fpCyto-13)

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

    Healthy

  1265. ICGi022-A-1 (SOD1-G128R_K7-4L-f and SOD1-G128R)

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

    Healthy subject

  1266. ICGi022-A-2 (SOD1-D91A and SOD1-D91A_K7-4Lf)

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

    Healthy subject

  1267. ICGi022-A-3 (K7-MYBPC3-N515del-1)

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

    Healthy subject

  1268. ICGi022-A-6 (K74-AsCas12a-N1-26)

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

    Healthy subject

  1269. ICGi022-A-7 (K74-AsCas12aY1-17)

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

    Healthy subject

  1270. ICGi026-A

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

    Fragile x syndrome

  1271. ICGi028-A (HCM4fm5.2)

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

    Hypertrophic cardiomyopathy

  1272. ICGi029-A (HCM14fm6.2)

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

    Hypertrophic cardiomyopathy

  1273. ICGi032-A

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

    Fragile x syndrome

  1274. ICGi033-A (77Q-17)

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

    Huntington disease

  1275. ICGi033-B (77Q-9)

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

    Huntington disease

  1276. ICGi033-C (77Q-20)

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

    Huntington disease

  1277. ICGi034-A (PD30-4-7)

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

    Obsolete_parkinson's disease

  1278. ICGi034-B (PD30-5-16)

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

    Obsolete_parkinson's disease

  1279. ICGi034-C (PD30-5-27)

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

    Obsolete_parkinson's disease

  1280. ICGi034-D (PD30-1)

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

    Obsolete_parkinson's disease

  1281. ICGi034-E (PD30-3)

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

    Obsolete_parkinson's disease

  1282. ICGi035-A (iCS-MAF1-1)

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

    Normal (average)

  1283. ICGi036-A (FH 1.3.1S)

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

    Hyperlipoproteinemia, type iia

  1284. ICGi037-A (FH 3.2.8T)

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

    Hyperlipoproteinemia, type iia

  1285. ICGi039-A (PD31-6)

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

    Normal (average)

  1286. ICGi039-B (PD31-7)

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

    Normal (average)

  1287. ICGi039-C (PD31-15)

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

    Normal (average)

  1288. ICGi042-B (PD12-5Lm)

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

    Parkinson disease

  1289. ICGi042-C (PD12-6Lm)

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

    Parkinson disease

  1290. ICGi043-A (LR-21)

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

    Parkinson disease

  1291. ICGi043-B (LR-2)

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

    Parkinson disease

  1292. ICGi043-C (LR-15)

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

    Parkinson disease

  1293. ICGi044-A (PD40-7)

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

    Parkinson disease

  1294. ICGi044-B (PD40-8)

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

    Parkinson disease

  1295. ICGi044-C (PD40-13)

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

    Parkinson disease

  1296. ICGi045-A (M-5)

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

    Rasopathy

  1297. ICGi046-A (V2-1)

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

    Rasopathy

  1298. ICGi052-A (PD57-6)

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

    Frontotemporal dementia

  1299. ICGi052-B (PD57-7)

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

    Frontotemporal dementia

  1300. ICGi053-A (PD58-4)

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

    Parkinson disease

  1301. ICGi053-B (PD58-7)

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

    Parkinson disease

  1302. ICGi053-C (PD58-14)

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

    Parkinson disease

  1303. ICGi054-B (PD69-2/1)

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

    Parkinson disease

  1304. ICGi054-C (PD69-4)

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

    Parkinson disease

  1305. ICGi058-A (iP63)

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

    Autism spectrum disorder

  1306. ICGi059-A (iHD46Q7.1)

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

    Huntington disease

  1307. ICGi060-C (PD92-39)

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

    Parkinson disease

  1308. ICHi003-A (TTNtv-003)

    Italy IRCCS Istituto Clinico Humanitas (ICH)
    Disease:

    Cardiomyopathy, dilated

  1309. ICMi001-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  1310. ICMi002-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  1311. ICMi003-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  1312. ICMi004-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  1313. ICMi005-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  1314. ICMi006-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  1315. ICMi007-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  1316. ICMi008-A

    France Institut du Cerveau (ICM) (ICM)
    Disease:

    Down syndrome

  1317. ICSSUi004-A

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

    Restrictive cardiomyopathy

  1318. IDIBGIi002-A (RB20234)

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

    Brugada syndrome

  1319. IDIBGIi003-A (​RB20235)

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

    Brugada syndrome

  1320. IDIBGIi005-A (RB20237)

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

    Normal (average)

  1321. IDIBGIi006-A (CPVT FiPS 51 EP6F-1 and RB20651)

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

    Catecholaminergic polymorphic ventricular tachycardia

  1322. IDIBGIi010-A (RB20655 and ​CPVT FiPS 55 EP6F-8)

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

    Normal (average)

  1323. IDMi001-A (K40)

    Germany Institute for Diabetes Research and Metabolic Diseases (IDM)
    Disease:

    Prediabetes syndrome

  1324. HMGUi001-A-4 (hiPSC-ARX-T2A-H2B-CFP-Flag)

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

    Normal (average)

  1325. HMGUi001-A-5 (ΔINK4 T2D risk region hiPSC)

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

    Normal (average)

  1326. HMGUi001-A-42 (NEUROD2 nVenus/nVenus iPSCs)

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

    Normal (average)

  1327. HMGUi001-A-43 (hINS-T2A-H2B-Cherry (-/-), hiPSC-INS-T2A-H2B-Cherry reporter and INSCherry/Cherry)

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

    Normal (average)

  1328. HMGUi001-A-46 (ARX-CFP/PAX4-mCherry, ARX-T2A-H2B-CFP/H2B-mCherry-RGSHis-T2A-PAX4 and ARXnCFP/nCFP/PAX4mCherry/mCherry)

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

    Normal (average)

  1329. IDVi001-A (iPS-NR2E3-86)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Retinitis pigmentosa

  1330. IDVi002-A (iPS-PRPF31-4138)

    France INSTITUT DE LA VISION (IDV)
    Disease:

    Normal (average)

  1331. IGGi002-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Cystic fibrosis

  1332. IGGi005-A (ZEB2 case 2)

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Mowat-wilson syndrome

  1333. IGGi006-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Caprin1

  1334. IGGi008-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Mowat-wilson syndrome

  1335. IGGi009-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Mowat-wilson syndrome

  1336. IGGi013-A

    Italy IRCCS Istituto Giannina Gaslini (IGG)
    Disease:

    Normal (average)

  1337. IGIBi011-A (GOC-13)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Spinocerebellar ataxia type 12

  1338. IGIBi013-A (FA_hiPSC_002)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Friedreich ataxia

  1339. IGIBi017-A (CT_hiPSC_001)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  1340. IGIBi018-A

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Rubinstein taybi like syndrome

  1341. IGIBi021-A (iPSC V3b)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  1342. IGIBi022-A (iPSC V2c)

    India CSIR-Institute of Genomics and Integrative Biology (IGIB)
    Disease:

    Normal (average)

  1343. IIMCBi003-A (K-Pic1)

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

    Normal (average)

  1344. IIMCBi006-A (M-T1)

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

    Huntington's disease

  1345. IIMCBi006-B (M-T2)

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

    Huntington's disease

  1346. IIMCBi007-A (jK-N1)

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

    Normal (average)

  1347. TECHe001-A (I3)

    Israel Technion - Israel Institute of Technology (IIT)

  1348. TECHe002-A (I4)

    Israel Technion - Israel Institute of Technology (IIT)

  1349. TECHe003-A (I6)

    Israel Technion - Israel Institute of Technology (IIT)

  1350. IMAGINi004-A (IMAGINE004)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  1351. IMAGINi005-A (IMAGINE005)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  1352. IMAGINi013-A (IMAGINE013)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  1353. IMAGINi021-A (IMAGINE021)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Normal (average)

  1354. IMAGINi070-A (IMAGINE070)

    France Imagine Institute / INSERM U1163 (IMAGIN)
    Disease:

    Meier-gorlin syndrome 1

  1355. IMBAi001-A (SCCF-176J clone#1 and HD.1 ARID1B+/+ clone 3a (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1356. IMBAi001-B (SCCF-176J clone#2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1357. IMBAi002-A (SCCF-177J clone#8)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1358. IMBAi004-A (SCCF-733J clone#1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1359. IMBAi004-B (SCCF-733J clone#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1360. IMBAi004-C (SCCF-733J clone#17)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1361. IMBAi005-B (SCCF-734J clone#3)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1362. IMBAi006-A (SCCF-735J clone#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1363. IMBAi006-B (SCCF-735J clone#17)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1364. IMBAi006-C (SCCF-735J clone#20)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1365. IMBAi007-A (SCCF-180J clone#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1366. IMBAi007-B (SCCF-180J clone#11)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1367. IMBAi008-A (SCCF-181J clone#16)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1368. IMBAi008-B (SCCF-181J clone#20)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1369. IMBAi008-C (SCCF-181J clone#24)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1370. IMBAi009-A (SCCF-179J clone#13)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1371. IMBAi009-B (SCCF-179J clone#15)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1372. IMBAi010-A (SCCF-2298J clone#1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1373. IMBAi010-B (SCCF-2298J clone#2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1374. IMBAi010-C (SCCF-2298J clone#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1375. IMBAi011-A (SCCF-736J clone#1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1376. IMBAi011-C (SCCF-736J clone#8)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Normal (average)

  1377. IMBAi013-A (DBA 14J #2)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Diamond-blackfan anemia 1

  1378. IMBAi014-A (DBA 15J #3)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Diamond-blackfan anemia 1

  1379. IMBAi015-A (DBA 16J #1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Diamond-blackfan anemia 1

  1380. IMBAi016-A (B001-ARID1B#10 and Pat.1 ARID1B+/- clone 1a (XY))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  1381. IMBAi017-A (B002-ARID1B#8 and Pat.2 ARID1B+/- clone 2a (XX))

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Coffin-siris syndrome

  1382. IMBAi018-A (622_DS04 #1)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Dravet syndrome

  1383. IMBAi019-A (623_DS22 #10)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Dravet syndrome

  1384. IMBAi020-B (624_DS40 #3)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Dravet syndrome

  1385. IMBAi021-A (TSC107J #5 and TSC#14 clone 107J#5)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  1386. IMBAi022-A (TSC112#4 and TSC#24 clone 112#4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  1387. IMBAi022-A-1 (TSC112#4r2c4)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  1388. IMBAi023-A (TSC#5 clone 32S and TSCp5#32S)

    Austria Institute of Molecular Biotechnology (IMBA)
    Disease:

    Tuberous sclerosis

  1389. IMBPASi001-A (iPSC-WFS1-#1)

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

    Wolfram syndrome 1

  1390. IMGTi001-B (iTAF5-32)

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

    Phelan-mcdermid syndrome

  1391. IMGTi003-A (iTAF6-6)

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

    Ring chromosome 13 syndrome

  1392. IMHe009-A (OZ-1)

    Turkey ISTANBUL MEMORIAL HOSPITAL (IMH)
    Disease:

    Chromosomal disease

  1393. IMHe012-A (NS-9)

    Turkey ISTANBUL MEMORIAL HOSPITAL (IMH)

  1394. IMHe013-A (NS-10)

    Turkey ISTANBUL MEMORIAL HOSPITAL (IMH)

  1395. IMOi003-A (STGD PBiPS3-SV4F-10)

    Spain Instituto de Microcirurgia Ocular - Grupo Miranza (IMO)
    Disease:

    Stargardt disease

  1396. INDBi001-A (INDB5.2.14)

    Germany Institute for Neuroanatomy and Developmental Biology, University of Tuebingen (INDB)
    Disease:

    Normal (average)

  1397. INDBi002-A

    Germany Institute for Neuroanatomy and Developmental Biology, University of Tuebingen (INDB)
    Disease:

    Normal (average)

  1398. INEUi003-A (FHL1-T)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Muscular dystrophy

  1399. INEUi005-A (FOXA2S229*-iPSCs)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Non-acquired combined pituitary hormone deficiency

  1400. INEUi006-A (DESS and IV-A hiPSC line)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Normal (average)

  1401. INEUi007-A (IV-B hiPSC line and DESY-HE)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Desminopathy

  1402. INEUi008-A (IV-C hiPSC line and DESJ)

    Argentina Instituto de Neurociencias Conicet (INEU)
    Disease:

    Desminopathy

  1403. INNDSUi003-A

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

    Becker muscular dystrophy

  1404. INNDSUi009-A

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

    Amyotrophic lateral sclerosis

  1405. INNDSUi010-A

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

    Dermatomyositis

  1406. INPERe002-A (Amicqui-2)

    Mexico Instituto Nacional de Perinatología (INPER)
    Disease:

    Normal (average)

  1407. INSAi002-A

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

    Fabry disease

  1408. INSAi003-A

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

    Mucolipidosis type ii

  1409. TMOi001-A-11

    France INSERM (INSRM)
    Disease:

    Cardiomyopathy

  1410. INSRMi013-A (PC179c1)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  1411. INSRMi021-A (PC177 3c14)

    France INSERM (INSRM)
    Disease:

    Myofibrillar myopathy 1

  1412. INSRMe013-A (STR-I-301-MFS)

    France INSERM (INSRM)
    Disease:

    Marfan syndrome

  1413. WAe009-A-G

    India Institute For Stem Cell Biology and Regenerative Medicine (INSTEM)
    Disease:

    Cancer

  1414. IPBi001-A (IPB-HD-001)

    South Korea iPSBIO (IPB)
    Disease:

    Huntington disease

  1415. IPBi002-A (IPB-HD-002)

    South Korea iPSBIO (IPB)
    Disease:

    Huntington disease

  1416. IPBi004-A (IPB-HD-004)

    South Korea iPSBIO (IPB)
    Disease:

    Huntington disease

  1417. IPBi101-A (IPB-WT-001)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1418. IPBi102-A (IPB-WT-002)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1419. IPBi103-A (IPB-WT-003)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1420. IPBi104-B (IPB-WT-004)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1421. IPBi105-A (IPB-WT-005)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1422. IPBi106-A (IPB-WT-006)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1423. IPBi107-A (IPB-WT-007)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1424. IPBi108-A (IPB-WT-008)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1425. IPBi110-A (IPB-WT-010)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1426. IPBi112-A (IPB-WT-012)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1427. IPBi113-A (IPB-WT-013)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1428. IPBi114-A (IPB-WT-014)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1429. IPBi115-A (IPB-WT-015)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1430. IPBi116-A (IPB-WT-016)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1431. IPBi117-A (IPB-WT-017)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1432. IPBi118-A (IPB-WT-018)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1433. IPBi119-A (IPB-WT-019)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1434. IPBi124-A (IPB-WT-024)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1435. IPBi126-A (IPB-WT-026)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1436. IPBi128-A (IPB-WT-028)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1437. IPBi129-A (IPB-WT-029)

    South Korea iPSBIO (IPB)
    Disease:

    Normal (average)

  1438. IPSCi001-A (IPSC-087-3)

    Taiwan iPSC Core (IPSC)
    Disease:

    Occult macular dystrophy

  1439. IPTi006-A (16M0065)

    China Institute of Pharmacology and Toxicology (IPT)
    Disease:

    Normal (average)

  1440. IRFMNi001-B-2 (CIone M CIITAKO-B2MKO)

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

    Normal (average)

  1441. IRFMNi003-A-4 (KO PKD1#5)

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

    Obsolete_autosomal dominant polycystic kidney disease

  1442. IRMBi001-A (AD-PS1 hiPSC)

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

    Obsolete_alzheimer's disease

  1443. IRMBi002-A (AD-APP hiPSC)

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

    Obsolete_alzheimer's disease

  1444. IRMBi004-A (CT4)

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

    Normal (average)

  1445. IRMBi005-A (SAD)

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

    Alzheimer disease

  1446. UCSFi001-A-1X

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

    Normal (average)

  1447. ISCRMi013-A (6832.2)

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

    Alzheimer's disease

  1448. ISCRMi016-A (6859.6)

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

    Normal (average)

  1449. ISCRMi026-A (7124.2)

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

    Alzheimer's disease

  1450. ISFi003-A (D2)

    Germany Institute for Stem Cell Research (ISF)
    Disease:

    Van maldergem syndrome 1

  1451. ISMMSi001-A (SAMEA104275576 and MFS44-E)

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

    Marfan syndrome

  1452. ISMMSi001-B (SAMEA104275577 and MFS44-16)

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

    Marfan syndrome

  1453. ISMMSi002-A (SAMEA104275578 and MFS60-12)

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

    Marfan syndrome

  1454. ISMMSi002-B (MFS60-3-1 and SAMEA104276575)

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

    Marfan syndrome

  1455. ISMMSi004-A (MSN01-02S)

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

    Normal (average)

  1456. ISMMSi013-A (MSN10-07S)

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

    Normal (average)

  1457. ISMMSi023-A (MSN20-06S)

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

    Normal (average)

  1458. ISMMSi027-A (MSN24-06S)

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

    Normal (average)

  1459. ISMMSi035-A (MSN32-04S)

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

    Normal (average)

  1460. ISMMSi038-A (MSN35-05S)

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

    Normal (average)

  1461. ISMMSi044-A (PLNR14del-1BC1)

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

    Cardiomyopathy

  1462. ISMMSi046-A (PLN-R14del-3BC7)

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

    Cardiomyopathy

  1463. ISMMSi049-A (PLN-1CC1)

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

    Normal (average)

  1464. ISMMSi060-A (CSI2101A)

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

    Combined oxidative phosphorylation defect type 25

  1465. ISTEMi002-A

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

    Glycogen storage disease type iii

  1466. ISTEMi004-A (CAC1, 7255_clG, 7255cloneG and 7255_CACNA1S-01 cloneG)

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

    Congenital myopathy 18

  1467. ISTEMi006-A (CAC3, 18169-clAA, 18169cloneAA and 18169_CACNA1S-03 cloneAA)

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

    Congenital myopathy 18

  1468. ISTEMi007-A (CAC4, 19895_clR, 19895_CACNA1S-04 cloneR and 19895cloneR)

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

    Congenital myopathy 18

  1469. ISTEMi011-A (WDR45 BPAN01 c02 and CO-A Cl2)

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

    Beta-propeller protein-associated neurodegeneration

  1470. ISTEMi012-A (WDR45 BPAN02 c04 and HE-M Cl4)

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

    Beta-propeller protein-associated neurodegeneration

  1471. ISTEMi013-A (WDR45 BPAN03 c05 and SI-A Cl5)

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

    Beta-propeller protein-associated neurodegeneration

  1472. ISTEMi013-B (WDR45 BPAN03 c12 and SI-A Cl12)

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

    Beta-propeller protein-associated neurodegeneration

  1473. ISTEMi017-A

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

    Danon disease

  1474. CEBe033-A-2 (SA001 Shank3 hetero1)

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

    Phelan-mcdermid syndrome

  1475. CEBe033-A-7 (SA001 Shank3 Homo3)

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

    Phelan-mcdermid syndrome

  1476. CEBe033-A-10 (SA001_WT_HGPRT_1)

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

    Lesch-nyhan syndrome

  1477. CEBe033-A-12 (SA001 DP427 KO1)

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

    Duchenne muscular dystrophy

  1478. CEBe033-A-13 (SA001 DP427 KO2)

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

    Duchenne muscular dystrophy

  1479. CEBe033-A-14 (SA001 DP140 KO1)

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

    Duchenne muscular dystrophy

  1480. CEBe033-A-15 (SA001 DP140 KO2)

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

    Duchenne muscular dystrophy

  1481. CEBe033-A-16 (SA001 DP140 KO3)

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

    Duchenne muscular dystrophy

  1482. CEBe033-A-18 (SA001 DP71 KO2)

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

    Duchenne muscular dystrophy

  1483. ITBi002-A (EP2B)

    Italy Institute for Biomedical Technologies (ITB)
    Disease:

    Developmental and epileptic encephalopathy 85 with or without midline brain defects

  1484. ITXi001-A (hERG CT Cl9)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  1485. ITXi003-A (MS368)

    France l’institut du thorax (ITX)
    Disease:

    Long qt syndrome

  1486. ITXi006-A-1 (IM-R406W)

    France l’institut du thorax (ITX)
    Disease:

    Desminopathy

  1487. ITXi007-A (202CT)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  1488. ITXi008-A (SD378M)

    France l’institut du thorax (ITX)
    Disease:

    Normal (average)

  1489. ITXi013-A (PT-R406W)

    France l’institut du thorax (ITX)
    Disease:

    Desminopathy

  1490. ITXi013-B (IC-R406)

    France l’institut du thorax (ITX)
    Disease:

    Desminopathy

  1491. IUFi002-A

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

    Leigh syndrome

  1492. WTSIi018-B-20

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

    Loss of function gene mutation

  1493. IUFi020-A (DU372r)

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

    Autoimmune encephalitis

  1494. JHUi005-A (HFD1)

    United States Johns Hopkins University (JHU)
    Disease:

    Marfan syndrome

  1495. JHUi006-A (HFD2 Clone 11)

    United States Johns Hopkins University (JHU)
    Disease:

    Marfan syndrome

  1496. JHUi007-A (i0195, Clone 5)

    United States Johns Hopkins University (JHU)
    Disease:

    Ehlers-danlos syndrome, vascular type

  1497. JHUi008-A (JHU001, clone 2)

    United States Johns Hopkins University (JHU)
    Disease:

    Normal (average)

  1498. JHUi009-A (JHU004 Clone 3)

    United States Johns Hopkins University (JHU)
    Disease:

    Ehlers-danlos syndrome, vascular type

  1499. JNCHi002-A (JNCHi002-A)

    China Jinan children's Hospital (JNCH)
    Disease:

    Familial hypercholesterolemia

  1500. JNCSRe001-A (BJNhem19)

    India Jawaharlal Nehru Centre for Advanced Scientific Research (JNCSR)

  1501. JNCSRe002-A (BJNhem20)

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

    Normal (average)

  1502. JNCSRe002-A-2 (BJNhem20-OCIAD2-CRISPR-40)

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

    Normal (average)

  1503. JNMUi002-A (JNMUi002-A)

    China Jining Medical University (JNMU)
    Disease:

    Schizophrenia

  1504. JTUi001-A

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

    Charge syndrome

  1505. JTUi002-A

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

    Waardenburg syndrome

  1506. JTUi005-A

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

    Neuronal intranuclear inclusion disease

  1507. JUCGRMi004-A (CMTA6)

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

    Charcot-marie-tooth disease

  1508. JUCGRMi005-A (JA5)

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

    Normal (average)

  1509. JUCTCi018-A

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

    Charcot-marie-tooth disease

  1510. JUFMDOi007-A

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

    Ush2a

  1511. KAIMRCi002-A (HLA-iPSC#1)

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

    Normal (average)

  1512. KAIMRCi003-A (DRVT-iPSC#1)

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

    Dravet syndrome

  1513. KAIMRCi011-A (LQTS-WT-iPSC#1)

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

    Normal (average)

  1514. KAIMRCi011-B (LQTS-WT-iPSC#2)

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

    Normal (average)

  1515. KAUSTi001-A (KS7-iPSC#A)

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

    Obsolete_klinefelter's syndrome

  1516. KAUSTi001-B (KS7-iPSC#B)

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

    Obsolete_klinefelter's syndrome

  1517. KAUSTi003-A (KS1-iPSC#D)

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

    Obsolete_klinefelter's syndrome

  1518. KAUSTi004-A (HM-iPSC#A)

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

    Normal (average)

  1519. KAUSTi004-B (HM-iPSC#B)

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

    Normal (average)

  1520. KAUSTi005-A (HB-iPSC#A)

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

    Normal (average)

  1521. KAUSTi005-B (HB-iPSC#B)

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

    Normal (average)

  1522. KAUSTi005-C (HB-iPSC#C)

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

    Normal (average)

  1523. KAUSTi006-A (KS6-iPSC#A)

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

    Obsolete_klinefelter's syndrome

  1524. KAUSTi006-B (KS6-iPSC#B)

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

    Obsolete_klinefelter's syndrome

  1525. KAUSTi007-A (KS2-iPSC#A)

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

    Obsolete_klinefelter's syndrome

  1526. KAUSTi007-B (KS2-iPSC#B)

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

    Obsolete_klinefelter's syndrome

  1527. KAUSTi008-A (KS4-iPSC#A)

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

    Obsolete_klinefelter's syndrome

  1528. KAUSTi008-B (KS4-iPSC#B)

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

    Obsolete_klinefelter's syndrome

  1529. KAUSTi008-C (KS4-iPSC#C)

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

    Obsolete_klinefelter's syndrome

  1530. KAUSTi008-D (KS4-iPSC#D)

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

    Obsolete_klinefelter's syndrome

  1531. KAUSTi008-E (KS4-iPSC#E)

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

    Obsolete_klinefelter's syndrome

  1532. KAUSTi008-F (KS4-iPSC#F)

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

    Obsolete_klinefelter's syndrome

  1533. KAUSTi008-G (KS4-iPSC#G)

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

    Obsolete_klinefelter's syndrome

  1534. KAUSTi009-A (KS3-iPSC#A)

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

    Obsolete_klinefelter's syndrome

  1535. KAUSTi009-B (KS3-iPSC#B)

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

    Obsolete_klinefelter's syndrome

  1536. KAUSTi010-A (KS5-iPSC#A)

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

    Obsolete_klinefelter's syndrome

  1537. KAUSTi010-B (KS5-iPSC#B)

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

    Obsolete_klinefelter's syndrome

  1538. KAUSTi011-A (iPSC-GLP1R-KO-C1)

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

    Developmental and epileptic encephalopathy

  1539. KAUSTi011-B (iPSC-GLP1R-KO-H4)

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

    Developmental and epileptic encephalopathy

  1540. WAe001-A-78 (H1X10 and H1X-10)

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

    Normal (average)

  1541. WAe001-A-82 (H1X-59 and H1X59)

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

    Normal (average)

  1542. WAe001-A-83 (H1.0-29 and H1.029)

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

    Normal (average)

  1543. WAe001-A-84 (H1.117 and H1.1-17)

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

    Normal (average)

  1544. WAe001-A-85 (H1.0102 and H1.0-102)

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

    Normal (average)

  1545. WAe001-A-87 (H1.213 and H1.2-13)

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

    Normal (average)

  1546. WAe001-A-88 (H1.2-124 and H1.2124)

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

    Normal (average)

  1547. WAe001-A-89 (H1.3-64 and H1.364)

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

    Normal (average)

  1548. WAe001-A-90 (H1.3-191 and H1.3191)

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

    Normal (average)

  1549. WAe001-A-91 (H1.4-126 and H1.4126)

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

    Normal (average)

  1550. WAe001-A-92 (H1.4-143 and H1.4143)

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

    Normal (average)

  1551. WAe001-A-93 (H1.5-23 and H1.523)

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

    Normal (average)

  1552. WAe001-A-94 (H1.528 and H1.5-28)

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

    Normal (average)

  1553. WAe001-A-96 (H1X-10/H1.0-31 and H1X10/H1.031)

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

    Normal (average)

  1554. WAe001-A-98 (H1X-10/H1.1-1 and H1X10/H1.11)

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

    Normal (average)

  1555. WAe001-A-99 (H1X-59/H1.1-13 and H1X59/H1.113)

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

    Normal (average)

  1556. WAe001-A-D (H1X-59/H1.3-68)

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

    Normal (average)

  1557. WAe001-A-E (H1X-10/H1.4-4)

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

    Normal (average)

  1558. WAe001-A-F (H1X-59/H1.4-5)

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

    Normal (average)

  1559. WAe001-A-I (H1.0-29/H1.1-13)

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

    Normal (average)

  1560. WAe001-A-K (H1.0-29/H1.2-31)

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

    Normal (average)

  1561. WAe001-A-Y (H1.2-13/H1.3-35)

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

    Normal (average)

  1562. WAe001-A-1A (H1.2-13/H1.4-69)

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

    Normal (average)

  1563. WAe001-A-1C (H1.2-13/H1.5-23)

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

    Normal (average)

  1564. WAe001-A-1E (H1.3-64/H1.1-37)

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

    Normal (average)

  1565. WAe001-A-1L (H1.4-143/H1.5-36)

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

    Normal (average)

  1566. KCGMHi001-A (KCGMH-CEP85L-K303-A4)

    Taiwan Kaohsiung Chang Gung Memorial Hospital (KCGMH)
    Disease:

    Lissencephaly

  1567. KCGMHi003-A (KCGMH-SCA8-K3143-A4)

    Taiwan Kaohsiung Chang Gung Memorial Hospital (KCGMH)
    Disease:

    Spinocerebellar ataxia type 8

  1568. KCLe009-A (KCL012_HD3)

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

    Huntington disease

  1569. KCLe010-A (KCL013_HD4)

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

    Huntington disease

  1570. KCLe011-A (KCL015_VHL2)

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

    Von hippel-lindau disease

  1571. KCLe012-A (KCL016_VHL3)

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

    Von hippel-lindau disease

  1572. KCLe013-A (KCL017_VHL4)

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

    Von hippel-lindau disease

  1573. KCLe014-A (KCL018_MD1)

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

    Myotonic dystrophy type 1

  1574. KCLe015-A (KCL011)

    United Kingdom King's College London (KCL)

  1575. KGUi001-A (AR1023)

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

    Obsolete_bipolar disorder

  1576. KIe001-A-1

    Sweden Karolinska Institutet (KI)
    Disease:

    Normal (average)

  1577. KIe007-A (HS346)

    Sweden Karolinska Institutet (KI)

  1578. KIe013-A (HS364)

    Sweden Karolinska Institutet (KI)

  1579. KIe013-A-1

    Sweden Karolinska Institutet (KI)

  1580. KIe019-A (HS401)

    Sweden Karolinska Institutet (KI)

  1581. KIe022-A (HS420)

    Sweden Karolinska Institutet (KI)

  1582. WAe009-A-99 (dCas9-p300 H9 21)

    South Korea Korea Institute of Toxicology (KIT)
    Disease:

    Normal (average)

  1583. KMUGMCi002-A (KMUGMCi002NIPBL)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Cornelia de lange syndrome

  1584. KMUGMCi004-A (KMUGMCi004APC and KN615)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Familial adenomatous polyposis

  1585. KMUGMCi006-E (TS271 #4 MT)

    Japan Kanazawa Medical University (KMUGMC)
    Disease:

    Tuberous sclerosis

  1586. KRIBBi005-A (CB-iPS-C7)

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

    Normal (average)

  1587. WAe009-A-95 (hTRF1-KO #3)

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

    Normal (average)

  1588. WAe009-A-96 (hTRF1-KO #6)

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

    None

  1589. WAe009-A-97 (hTRF1-KO #9)

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

    None

  1590. KSCBi001-A (hUSiPS2)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  1591. KSCBi005-A-3 (CMC-003i-Pdx1.EGFP and CMC-hiPSC-003(PDX1-GFP))

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  1592. KSCBi006-A (KNIH-OI001i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Osteogenesis imperfecta type 1

  1593. KSCBi007-A (KNIH-PWS001i-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Prader-willi syndrome

  1594. KSCBi010-A (DKH005i-A and DKHi005-A)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Senior-loken syndrome

  1595. KSCBi017-A-1 (PB01-EiPS21_GATA6-EGFP)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  1596. KSCBi017-A-2

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Normal (average)

  1597. KSCBi024-A (Down syndrome-EiPSC)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Down syndrome

  1598. KSCBi026-A (KNIH-LQT13-hiPSC, DPHCi13 and LQT-13)

    South Korea National Stem Cell Bank (KSCB)
    Disease:

    Atrial fibrillation

  1599. BIONi010-C-56 (BIONi010-C-A713T-C25)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  1600. BIONi010-C-57 (BIONi010-C-A713T-C42)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  1601. BIONi010-C-58 (BIONi010-C-A713T-C1)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  1602. BIONi010-C-59 (BIONi010-C-A713T-C33)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  1603. BIONi010-C-60 (BIONi010-C-R589C-C7)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  1604. BIONi010-C-61 (BIONi010-C-R589C-C16)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  1605. BIONi010-C-62 (BIONi010-C-R589C-C5)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  1606. BIONi010-C-63 (BIONi010-C-R589C-C9)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  1607. KUi013-A (SK)

    Denmark University of Copenhagen (KU)
    Disease:

    Normal (average)

  1608. KUi013-A-1 (SK GC)

    Denmark University of Copenhagen (KU)
    Disease:

    Obsolete_epilepsy

  1609. WAe009-A-2C (H9-CRISPRi)

    Denmark University of Copenhagen (KU)
    Disease:

    None

  1610. KUe013-A (LRB016)

    Denmark University of Copenhagen (KU)

  1611. KUIFMSi009-A (243H1)

    Japan Kyoto University (KUIMS)

  1612. KUIFMSi009-B (243H7)

    Japan Kyoto University (KUIMS)

  1613. KUIFMSi011-A (246G1)

    Japan Kyoto University (KUIMS)

  1614. KUIFMSi011-B (246G3)

    Japan Kyoto University (KUIMS)

  1615. KUIFMSi011-C (246G4)

    Japan Kyoto University (KUIMS)

  1616. KUIFMSi011-D (246G5)

    Japan Kyoto University (KUIMS)

  1617. KUIFMSi011-E (246G6)

    Japan Kyoto University (KUIMS)

  1618. SIGi001-A-24 (SIGi001-HC3x-ICAM1-GFP)

    Belgium KU Leuven (KUL)
    Disease:

    Normal (average)

  1619. KUMi003-A

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

    Obsolete_acute promyelocytic leukemia

  1620. KUMi006-A

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

    Obsolete_multiple myeloma

  1621. KUMCi001-A (ALLCD34+)

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

    Acute lymphoblastic leukemia

  1622. LBi002-B (PH-BL-002 Clone 9 and iLB-272bfs9)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  1623. LBi005-A (iLB-293bms257 and PH-BL-411 Clone 257)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  1624. LBi005-B (iLB-293bms258 and PH-BL-411 Clone 258)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  1625. LBi006-A (PH-BL-102 Clone 16 and iLB-269bms16)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  1626. LBi006-B (iLB-269bms8 and PH-BL-102 Clone 8)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  1627. LBi008-A (PH-BL-407 Clone 128 and iLB-289bms128)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  1628. LBi013-A (PH-BL-304 Clone 117 and iLB-279bfs117)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  1629. LBi014-A (iLB-281bfs191 and PH-BL-402 Clone 191)

    Germany Life & Brain GmbH (LB)
    Disease:

    Alzheimer disease

  1630. LCPHi001-A

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

    Obsolete_parkinson's disease

  1631. LCSBi001-A (VPS35 1_2)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Obsolete_parkinson's disease

  1632. LCSBi009-A-1 (RHOT1_R272Q_clone18_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  1633. LCSBi010-A-1 (RHOT1_R450C_clone6_IsogenicControl)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  1634. LCSBi013-A (GL2)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  1635. LCSBi015-A (S2 Cl4 and 89732)

    Luxembourg Luxembourg Centre for Systems Biomedicine (LCSB)
    Disease:

    Parkinson disease

  1636. LEIi004-A

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  1637. LEIi004-A-1

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  1638. LEIi005-A

    Australia Lions Eye Institute (LEI)
    Disease:

    Retinitis pigmentosa

  1639. LEIi021-B (1577ips9)

    Australia Lions Eye Institute (LEI)
    Disease:

    Normal (average)

  1640. LIBDi022-A (4003.07)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  1641. LIBDi023-A (4004.04)

    United States Lieber Institute (LIBD)
    Disease:

    Normal (average)

  1642. LINi001-A (Linea 1)

    Canada LineaBio (LIN)
    Disease:

    Normal (average)

  1643. UCSFi001-A-72 (FUS-R521G HET 2B10 and LSUHSi004-A-72)

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

    Amyotrophic lateral sclerosis

  1644. UCSFi001-A-73 (FUS-R521G HOM 1D9)

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

    Amyotrophic lateral sclerosis

  1645. LUi001-A (CALP1.3)

    Latvia University of Latvia (LU)
    Disease:

    Calpain-3-related limb-girdle muscular dystrophy r1

  1646. LUi002-A (CALP2.2)

    Latvia University of Latvia (LU)
    Disease:

    Calpain-3-related limb-girdle muscular dystrophy r1

  1647. LUBi001-B (PGRN-8310, RCFB58 c4.4, PGRN8310 and RCi194)

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

    Frontotemporal dementia

  1648. LUEi013-A (iPS-L-2135)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Normal (average)

  1649. LUEi018-A (iPS-L-2124)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Parkinson disease

  1650. LUEi020-A-1 (iPS-L9827-6_TOR1A_WT-3xFLAG/dGAG)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  1651. LUEi020-A-3 (iPS-L9827-6_TOR1A_dGAG-3xFLAG/dGAG)

    Germany Institute of Neurogenetics (LUE)
    Disease:

    Autosomal dominant torsion dystonia 1

  1652. LUMCi002-B (113-7 and LUMC0113iATAX07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Spinocerebellar ataxia type 1

  1653. LUMCi003-A (114-1 and LUMC0114iCTRL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  1654. LUMCi003-B (114-2 and LUMC0114iCTRL02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  1655. LUMCi004-A-1 (LU99_AAVS1-bxb-v2)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  1656. LUMCi004-A-2 (LU99_CLYBL-bxb-v2)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  1657. LUMCi004-A-3 (LUMCi099_XPA_B8)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Xeroderma pigmentosum group a

  1658. LUMCi004-A-4 (LUMCi099_XPC_D10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Xeroderma pigmentosum group c

  1659. LUMCi004-A-5 (LU99_SCN5A-R282H_cis)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Brugada syndrome

  1660. LUMCi004-A-6 (LU99_SCN5A-R282H_trans)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Brugada syndrome

  1661. LUMCi004-A-7 (LU99-04_AAVS-bxb-dual)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  1662. LUMCi004-A-8 (LU99 CLYBL-Bxb-v3_Dual and LUMC0099iCLYBL-06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  1663. LUMCi007-A (LUMC0151iHD01 and 151-1)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  1664. LUMCi008-C (152-4 and LUMC0152iHD04)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Huntington disease

  1665. LUMCi013-A (LUMC0133iCTRL06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  1666. LUMCi016-A (LUMC0136iCTRL09)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  1667. LUMCi017-A (LUMC0111iALK and LUMC0111iALK07)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  1668. LUMCi018-A (LUMC0112iALK and LUMC0112iALK08)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  1669. LUMCi028-A (LUMC0020iCTRL06 and FLB6)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  1670. LUMCi029-A (LUMC0072iCTRL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  1671. LUMCi029-A-2 (IsoLUMC0072iENG p.Met1Val-F5)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 1

  1672. LUMCi029-A-3 (IsoLUMC0072iALK1Het(p.Gly48Glu))

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Telangiectasia, hereditary hemorrhagic, type 2

  1673. LUMCi029-B (LUMC0004iCTRL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Normal (average)

  1674. LUMCi045-A (LUMC0145iKLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  1675. LUMCi045-A-1 (iso01LUMC0145iKLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  1676. LUMCi046-A (LUMC0146iKLHL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  1677. LUMCi046-A-1 (iso2LUMC0146iKLHL10)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  1678. LUMCi059-A (LUMCi232KLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  1679. LUMCi059-A-1 (Iso71LUMCi232KLHL01)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Intermediate epidermolysis bullosa simplex with cardiomyopathy

  1680. LUMCi062-A (LUMC0322iFOPA-03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Single ventricle defect

    Disease:

    Congenital abnormality

  1681. LUMCi062-A-2 (iso2LUMC0322iFOPA-03)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Single ventricle defect

    Disease:

    Congenital abnormality

  1682. LUMCi062-C (LUMC0322iFOPA-06)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Single ventricle defect

    Disease:

    Congenital abnormality

  1683. LUMCi065-A (LUMC0201iCSC02)

    Netherlands Leiden University Medical Center (LUMC)
    Disease:

    Central serous chorioretinopathy

  1684. LUMCi070-C (APPV742L Clone K)

    Netherlands Leiden University Medical Center (LUMC)

  1685. LVPEIi001-A (hiPSC-F2-3F1, LVIP01-NC-F2-1 and F2-4F)

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

    Normal (average)

  1686. LVPEIi001-B (LVIP02-NC-F2-1)

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

    Normal (average)

  1687. LVPEIi002-A (LVIP02-RB-1)

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

    Retinoblastoma

  1688. RUCDRi002-A-64 (LVIP05-RB1-CS2)

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

    Retinoblastoma

  1689. LVPEIi006-A (LVIP02-LC12-1)

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

    Leber congenital amaurosis 12

  1690. LVPEIi006-B (LVIP04-LC12-1)

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

    Leber congenital amaurosis 12

  1691. LVPEIi006-B-1 (LVIP04-LC12-1-BE1 and VS-CTS-RD3-BE1, Clone 27)

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

    Leber congenital amaurosis 12

  1692. LVPEIi007-B (LVIP04-SD1-1)

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

    Stargardt disease

  1693. LVPEIi008-A (LVIP02-SD1-2)

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

    Stargardt disease

  1694. LZUSHi002-A

    China Lanzhou University Second Hospital (LZUSH)
    Disease:

    Madd

  1695. MCRIi001-A (PB001)

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

    Normal (average)

  1696. MCRIi035-B (MCRIi-TC160154-UC-cl5)

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

    Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

  1697. MDCi007-A (8993-A12)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  1698. MDCi008-A (8993-B12)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  1699. MDCi009-A (8993-C11)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  1700. MDCi010-A (8993-D7)

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Leigh disease

  1701. MDCi013-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  1702. MDCi013-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  1703. MDCi014-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  1704. MDCi014-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Normal (average)

  1705. WTSIi018-B-26 (Kolf 2.1 J (FUS R521H WT/SNV))

    United Kingdom Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Amyotrophic lateral sclerosis

  1706. MDCi233-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Limb-girdle muscular dystrophy type 2b

  1707. MDCi233-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Limb-girdle muscular dystrophy type 2b

  1708. MDCi237-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Maternally-inherited leigh syndrome

  1709. MDCi237-B

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Maternally-inherited leigh syndrome

  1710. MDCi238-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Maternally-inherited leigh syndrome

  1711. MDCi239-A

    Germany Max Delbrück Center Berlin Buch (MDC)
    Disease:

    Narp syndrome

  1712. METUi002-A

    Turkey Middle East Technical University (METU)

  1713. MHHi001-A (hHSC_Iso4_ADCF_SeViPS2 (Phönix))

    Germany Hannover Medical School (MHH)
    Disease:

    Normal (average)

  1714. MHHi029-A (F01 #20)

    Germany Hannover Medical School (MHH)

  1715. MHRCCGi001-A (P1SH)

    Russia Laboratory Clinical Genetics (MHRCCG)
    Disease:

    Schizophrenia

  1716. MHRCCGi005-A (A2SH)

    Russia Laboratory Clinical Genetics (MHRCCG)
    Disease:

    Normal (average)

  1717. MILi001-A (K10 and hFF-iPSCs)

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

    Normal (average)

  1718. MIPTi001-A (NAA)

    Russia Moscow Institute of Physics and Technology (MIPT)
    Disease:

    X-linked adrenoleukodystrophy

  1719. MIPTi002-A

    Russia Moscow Institute of Physics and Technology (MIPT)
    Disease:

    Obsolete_hyperparathyroidism

  1720. MIZMe013-A (Miz-hES11)

    South Korea MizMedi Hospital (MIZM)

  1721. MLi002-A-1 (iso-hiEBS and hiEBS clone 8)

    Netherlands Faculty of Medicine University of Ljubljana (ML)
    Disease:

    Epidermolysis bullosa simplex

  1722. MLUi001-M

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

    Schizophrenia

  1723. MNDi002-A (MND-Nek1-P002)

    Germany Institut für Anatomie und Zellbiologie, Universität Ulm (MND)
    Disease:

    Amyotrophic lateral sclerosis

  1724. MNZTASi004-A (MS_0003)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Obsolete_relapsing-remitting multiple sclerosis

  1725. MNZTASi005-A (MS_0006)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Obsolete_relapsing-remitting multiple sclerosis

  1726. MNZTASi009-A (MS_0009.1)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Normal (average)

  1727. MNZTASi031-C (MS_0031.3)

    Australia Menzies Institute for Medical Research (MNZTAS)
    Disease:

    Secondary progressive multiple sclerosis

  1728. MONUi002-A (86202443.3)

    Australia Monash University (MONU)
    Disease:

    Obsolete_autism spectrum disorder

  1729. MPIi001-A

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Normal (average)

  1730. MPIi003-A-1 (IM2GC and L2-2GC)

    Germany Max Planck Institute for Molecular Biomedicine (MPI)
    Disease:

    Obsolete_parkinson's disease

  1731. MPIPi058-A (UL4)

    Germany Max Planck Institute of Psychiatry (MPIP)
    Disease:

    Progressive myoclonic epilepsy type 1

  1732. MRIi003-A (HK)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  1733. MRIi003-A-2 (MYH10-/-)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  1734. MRIi003-A-3 (TRPM4+/-)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Normal (average)

  1735. MRIi016-A (Shox2.1)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Atrial fibrillation

  1736. MRIi018-A (HLHS_375)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Hypoplastic left heart syndrome

  1737. MRIi024-A (Shox2.2)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Atrial fibrillation

  1738. MRIi025-A (Noonan 3a)

    Germany Klinikum rechts der Isar (MRI)
    Disease:

    Noonan syndrome

  1739. WAe009-A-1I (H9::GFP cyto-reporter line)

    United States Memorial Sloan Kettering Cancer Center (MSK)
    Disease:

    Normal (average)

  1740. MUi010-A (MYH9)

    Thailand Mahidol University (MU)
    Disease:

    Myh9-related syndromic thrombocytopenia

  1741. MUi015-A (RB1)

    Thailand Mahidol University (MU)
    Disease:

    Retinoblastoma

  1742. MUi028-A

    Thailand Mahidol University (MU)
    Disease:

    Normal (average)

  1743. MUi032-A

    Thailand Mahidol University (MU)
    Disease:

    Choroideremia

  1744. MUi033-A (MU020 and homoHbE iPSC)

    Thailand Mahidol University (MU)
    Disease:

    Normal (average)

  1745. MUi040-A

    Thailand Mahidol University (MU)
    Disease:

    Amyloidosis

  1746. MUBi002-A (CF 001)

    Poland Medical University of Bialystok (MUB)
    Disease:

    Cystic fibrosis

  1747. MUNIi001-A (DMD02)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  1748. MUNIi002-A (MDMD02)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  1749. MUNIi003-A (DMD03)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  1750. MUNIi004-A (DMD04)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Duchenne muscular dystrophy

  1751. MUNIi010-A (WTF80, fHC3, fWT3 and fCTRL3)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  1752. MUNIi012-A (BAD2 and sAD2)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer's disease

  1753. MUNIi013-A (BAD4 and sAD3)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Alzheimer's disease

  1754. MUNIi019-A (NBS-M and NBS)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Nijmegen breakage syndrome

  1755. MUNIe006-A (CCTL 13)

    Czech Republic Masaryk University (MUNI)

  1756. MUNIe008-A (MUES 8)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  1757. MUNIe009-A (MUES 9)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  1758. MUNIe013-A (MUES 6)

    Czech Republic Masaryk University (MUNI)
    Disease:

    Normal (average)

  1759. MURAi001-A (TET1mutationC18)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)

  1760. MURAi002-A (-4bp/HbE C11)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Hemoglobin e-beta-thalassemia syndrome

  1761. MURAi003-A (HoHLA, Homozygous-HLA and HoHLA C3)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Normal (average)

  1762. MURAi004-A (Bart)

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Junctional epidermolysis bullosa

  1763. MURAi007-A

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Inherited retinal dystrophy

  1764. MURAi009-A

    Thailand Faculty of Medicine Ramathibodi Hospital (MURA)
    Disease:

    Normal (average)

  1765. MUSIi001-A-1 (B2M-KO-SFiPSC5 and HLA-I-null SFiPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  1766. MUSIi001-A-3 (TIGIT-KO-SFiPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  1767. MUSIi004-A

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Spinocerebellar ataxia type 3

  1768. MUSIi013-A (CBNK-iPSC)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  1769. MUSIi013-A-2 (CAR-TIM3 iPSCs)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  1770. MUSIi017-A (Oneg)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  1771. MUSIi019-A (SLC4A1-21-C1)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Distal renal tubular acidosis

  1772. MUSIi023-A (hmziPSC and Homozygous HLA iPSC)

    Thailand Faculty of Medicine Siriraj Hospital (MUSI)
    Disease:

    Normal (average)

  1773. NCAi001-A

    Netherlands Ncardia B.V. (NCA)
    Disease:

    Normal (average)

  1774. WAe009-A-3I

    United States National Institutes of Health - National Center for Advancing Translational Sciences (NCATS)
    Disease:

    Normal (average)

  1775. WAe009-A-3J

    United States National Institutes of Health - National Center for Advancing Translational Sciences (NCATS)
    Disease:

    Normal (average)

  1776. WAe007-A-3 (DNAJC19 KO)

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

    Dilated cardiomyopathy with ataxia

  1777. WAe009-A-91

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

    Barth syndrome

  1778. NCHi004-A (NCH140)

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

    Down syndrome

  1779. NCHi006-A (NCH023)

    United States Nationwide Children's Hospital (NCH)

  1780. NCHi013-A (NCH17)

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

    Pulmonary valve atresia with intact ventricular septum

  1781. NCHi024-A (NCH27)

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

    Bicuspid aortic valve

  1782. NCSi001-A (NCS065)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Alzheimer's disease

  1783. NCSi003-A (NCS067)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Normal (average)

  1784. NCSi005-A (NCS069)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Alzheimer's disease

  1785. NCSi007-A (NCS071)

    Norway Norwegian Center for Stem Cell Research (NCS)
    Disease:

    Alzheimer's disease

  1786. NEIi001-A (iPSC-F34)

    United States National institutes of Health (NEI)
    Disease:

    Opa1-related optic atrophy with or without extraocular features

  1787. NEIi003-A (iPSC-F36)

    United States National institutes of Health (NEI)
    Disease:

    Opa1-related optic atrophy with or without extraocular features

  1788. NENCKIi004-A (MPAN-22.3)

    Poland Nencki Institute of Experimental Biology PAS (NENCKI)
    Disease:

    Mitochondrial membrane protein-associated neurodegeneration

  1789. NERCe002-A (chHES-90)

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

    Normal (average)

  1790. NERCe002-A-1 (chHES-90-PLEX-ZsGreen)

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

    Normal (average)

  1791. NERCe002-A-2 (chHES-90-PLEX-Luciferase)

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

    Normal (average)

  1792. NERCe002-A-3 (chHES-90-pINDUCER20-tet-14-3-3ζ)

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

    Normal (average)

  1793. NERCe003-A (chHES-8)

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

    Normal (average)

  1794. NHGRIi001-A (iPSC-1 and FISAL04_Sia80)

    United States National Human Genome Research Institute (NHGRI)

  1795. NHLBIi001-B (MS19-ES-H)

    United States NHLBI iPSC Core (NHLBI)
    Disease:

    Normal (average)

  1796. NIHTVBi024-A

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

  1797. NIHTVBi025-A

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

    Sting-associated vasculopathy with onset in infancy

  1798. NIHTVBi028-A

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

    Lyn gene mutation

  1799. NIMHi005-A

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

    Normal (average)

  1800. NIMHi008-A (NphyiALS1)

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

    Amyotrophic lateral sclerosis

  1801. NIMHi009-A

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

    Normal (average)

  1802. NIMHi013-A

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

    Epilepsy

  1803. NIMHi015-A

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

    Autosomal recessive juvenile parkinson disease 2

  1804. NIMHi018-A (PD07)

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

    Parkinson's disease 6

  1805. NJDTHi001-A

    China Department of Cardio-Thoracic Surgery, Nanjing Drum Tower Hospital (NJDTH)
    Disease:

    Danon disease

  1806. NMIi002-A

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

    Schizophrenia

  1807. NMIi002-B

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

    Schizophrenia

  1808. NMIi004-A

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

    Schizophrenia

  1809. NMIi006-B

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

    Schizophrenia

  1810. NMIi010-A

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

    Normal (average)

  1811. NMIi012-A (DG1)

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

    Breast carcinoma

  1812. NMIi012-B (DG2)

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

    Breast carcinoma

  1813. NMIi012-D (DG4)

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

    Breast carcinoma

  1814. NMIi012-E (DG5)

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

    Breast carcinoma

  1815. NOVOe001-A (3053)

    Sweden Novo Nordisk A/S (NOVO)

  1816. CEBe012-A-1 (HLAE0101cl.2A)

    Denmark Novo Nordisk A/S (NOVO)

  1817. NSi003-A (NSi-DS)

    India Stem Cell and Neurobiology Lab (NS)
    Disease:

    Down syndrome

  1818. NSi003-B (NSi-isoEu)

    India Stem Cell and Neurobiology Lab (NS)
    Disease:

    Down syndrome

  1819. NUIGi004-A (LQT003C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  1820. NUIGi011-C (LQTS010Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 1

  1821. NUIGi012-A (LQT011C8)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  1822. NUIGi018-A (LQT017C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  1823. NUIGi020-A (LQT019C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 2

  1824. NUIGi038-B (LQTH002Cx)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  1825. NUIGi038-B-1 (CR.LQTH002Cx-A17)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Long qt syndrome 3

  1826. NUIGi038-C (LQTH002C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  1827. NUIGi044-B (ALS69C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  1828. NUIGi048-C (ALSH84C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  1829. NUIGi049-A (ALSH47C1)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  1830. NUIGi051-B (ALS57C3)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Obsolete_sporadic amyotrophic lateral sclerosis

  1831. NUIGi052-A

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Non-specific early-onset epileptic encephalopathy

  1832. NUIGi052-C

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Non-specific early-onset epileptic encephalopathy

  1833. NUIGi055-A (iPSC C1-15)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  1834. NUIGi059-A (EP2001 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Epileptic encephalopathy

  1835. NUIGi059-B (EP2001 C5)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Epileptic encephalopathy

  1836. NUIGi060-B (EP2C001 C2)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  1837. NUIGi064-C (EP2C003 C4)

    Ireland National University of Ireland Galway (NUIG)
    Disease:

    Normal (average)

  1838. NUMNi001-A

    Japan Department of Nephrology, Nagoya University Hospital (NUMN)
    Disease:

    Normal (average)

  1839. NUMNi003-A

    Japan Department of Nephrology, Nagoya University Hospital (NUMN)
    Disease:

    Autosomal dominant polycystic kidney disease

  1840. NYSCFi001-C (AL0002-01-SV-008)

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

    Normal (average)

  1841. NYSCFe003-A (NY0003-01-ES-001)

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

    Normal (average)

  1842. ORIONi001-A (iALS-1)

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

    Obsolete_sporadic amyotrophic lateral sclerosis

  1843. ORIONi004-A (iDMD-2)

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

    Duchenne and becker muscular dystrophy

  1844. OSRi005-A (ND#68)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Normal (average)

  1845. OSRi013-A (OSR_001#10)

    Italy Ospedale San Raffaele (OSR)
    Disease:

    Multiple sclerosis

  1846. OTATi002-A (HC8)

    United States Office of Tissues and Advanced Therapies, CBER, FDA (OTAT)
    Disease:

    Normal (average)

  1847. PCIi009-A (PC168)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  1848. PCIi010-A (PC169)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  1849. PCIi011-A (PC170)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  1850. PCIi015-A (PC191)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  1851. PCIi016-A (PC192)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  1852. PCIi019-A (PC200)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  1853. PCIi021-A (PC202)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  1854. PCIi023-A (PC204)

    France PHENOCELL (PCI)
    Disease:

    Normal (average)

  1855. PCIi025-A (PC084)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  1856. PCIi026-A (PC085)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  1857. PCIi027-A (PC086)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  1858. PCIi031-A (PC079)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome type 1

  1859. PCIi032-A (PC087)

    France PHENOCELL (PCI)
    Disease:

    Waardenburg syndrome

  1860. PCIi034-A (PC138)

    France PHENOCELL (PCI)
    Disease:

    Aicardi-goutieres syndrome

  1861. WTSIi018-B-13

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Ataxia telangiectasia syndrome

  1862. PEIi021-A (PEIi004-A)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  1863. PEIi021-B (PEIi004-B)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  1864. PEIi021-C (PEIi004-C)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  1865. PEIi021-D (PEIi004-D)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  1866. PEIi022-A (PEIi005-A)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  1867. PEIi022-B (PEIi005-B)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  1868. PEIi022-C (PEIi005-C)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  1869. PEIi022-D (PEIi005-D)

    Germany Paul-Ehrlich-Institut (PEI)
    Disease:

    Leukocyte adhesion deficiency type 1

  1870. PENNi001-A (PENN123i-SV20 and SV20)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  1871. PENNi001-A-1 (SV20 ACE2KO D1)

    United States University of Pennsylvania (PENN)
    Disease:

    Normal (average)

  1872. PENNi003-A (HPAP021 Sev2)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  1873. PENNi009-A (HPAP149 Sev3)

    United States University of Pennsylvania (PENN)
    Disease:

    Type 1 diabetes mellitus

  1874. RCi001-A (Thp3C-6 and RCi88)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  1875. RCi001-B (RCi89 and Thp3C-9)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Primary erythromelalgia

  1876. RCi003-A (RCi115 and CIP11A-5)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Obsolete_pain agnosia

  1877. RCi003-B (CIP11A-9 and RCi117)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Obsolete_pain agnosia

  1878. PFIZi009-A (RCi188)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  1879. PFIZi010-A (FB65c7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  1880. PFIZi010-B (FB65c16)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  1881. PFIZi010-C (FB65c20)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  1882. PFIZi012-A (FB66c17 and RCi198)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Chromosome 16p11.2 deletion syndrome, 220-kb

  1883. PFIZi013-A (RCi215 and RCFB59 C9)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Amyotrophic lateral sclerosis

  1884. PFIZi014-A (OD002-s7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  1885. PFIZi015-A (OD003-s5)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  1886. PFIZi018-A (BC143c8 and RCi207)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  1887. PFIZi019-A (RCi202 and BC145c6)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  1888. PFIZi021-A (OD001-s7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Dravet syndrome

  1889. PFIZi022-A (B219c2)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epileptic encephalopathy

  1890. PFIZi023-A (B217c8)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Bilateral frontoparietal polymicrogyria

  1891. PFIZi024-A (B218c6)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Obsolete_epilepsy

  1892. PFIZi025-A (B220c16)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Obsolete_epilepsy

  1893. PFIZi027-A (B221c13)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Lissencephaly

  1894. PFIZi028-A (B212c7)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Neurodevelopmental disorder

  1895. PFIZi030-A (B216c13)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Acromesomelic dysplasia

  1896. PFIZi031-A (B213c1)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Epileptic encephalopathy

  1897. PFIZi032-A (B214c8)

    United Kingdom Pfizer Limited - Pfizer (PFIZ)
    Disease:

    Tuberous sclerosis

  1898. PGNMi001-A (AG08C5)

    France Institut NeuroMyoGene - Pathophysiology and Genetics of Neuron and Muscle (INMG-PGNM) (PGNM)
    Disease:

    Normal (average)

  1899. PHAi003-A (PIDi003-A)

    Sweden Pan-Hammarström laboratory (PHA)
    Disease:

    Primary immunodeficiency

  1900. PNURCKi003-A (CK-iDS1)

    South Korea Pusan National University Yangsan Hospital, Rare Disease Center (PNURCK)
    Disease:

    Desanto-shinawi syndrome

  1901. PNUSCRi002-A (GBA PD iPSC9)

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

    Parkinson disease

  1902. PNUSCRi003-A (GBA Gaucher iPSC1)

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

    Gaucher disease

  1903. PNUSCRi004-A (GBA PD iPSC8)

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

    Parkinson disease

  1904. PNUSCRi006-A (Sanfilippo hiPSCs)

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

    Sanfilippo syndrome

  1905. PNUYHi002-A

    South Korea Pusan National University Yangsan Hospital (PNUYH)
    Disease:

    Alzheimer's disease

  1906. PNUYHi003-A

    South Korea Pusan National University Yangsan Hospital (PNUYH)
    Disease:

    Neuronal intranuclear inclusion disease

  1907. PUMCHi001-A (IPS-34)

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Familial partial lipodystrophy type 2

  1908. PUMCHi020-A

    China Peking Union Medical College Hospital (PUMCH)
    Disease:

    Aicardi-goutieres syndrome

  1909. QBRIi005-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Psoriasis

  1910. QBRIi006-C

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_psoriasis

  1911. QBRIi007-A (GLUT2 Mut-int iPSCs)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Fanconi-bickel syndrome

  1912. QBRIi013-A

    Qatar Qatar Biomedical Research Institute (QBRI)

  1913. QBRIi015-A (NDD04 and hiPSC_11080404_c1)

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  1914. QBRIi019-A

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  1915. QBRIi021-B

    Qatar Qatar Biomedical Research Institute (QBRI)
    Disease:

    Obsolete_autism spectrum disorder

  1916. RAUi001-A

    Armenia Russian-Armenian University (RAU)
    Disease:

    Normal (average)

  1917. RAUi001-B

    Armenia Russian-Armenian University (RAU)
    Disease:

    Normal (average)

  1918. RAUi001-C

    Armenia Russian-Armenian University (RAU)
    Disease:

    Normal (average)

  1919. RAUi002-A

    Armenia Russian-Armenian University (RAU)
    Disease:

    Familial mediterranean fever

  1920. RBi001-A (fb101 and RB101)

    United Kingdom R Biomedical (RB)
    Disease:

    Normal (average)

  1921. RCi004-A (PDSC-10 and RCi150)

    United Kingdom Roslin Cells (RC)
    Disease:

    Huntington disease

  1922. RCi004-B (RCi68 and PDSC-3)

    United Kingdom Roslin Cells (RC)
    Disease:

    Huntington disease

  1923. RCe010-A (RC-6 and RC6)

    United Kingdom Roslin Cells (RC)
    Disease:

    Monogenic disease

  1924. RCe013-A (RC9 and RC-9)

    United Kingdom Roslin Cells (RC)

  1925. RCe014-A (RC10 and RC-10)

    United Kingdom Roslin Cells (RC)

  1926. RCe017-A (RC13 and RC-13)

    United Kingdom Roslin Cells (RC)
    Disease:

    Normal (average)

  1927. RCe017-A-1

    United Kingdom Roslin Cells (RC)
    Disease:

    Normal (average)

  1928. RCe020-A (RC-16 and RC16)

    United Kingdom Roslin Cells (RC)
    Disease:

    Normal (average)

  1929. RCMGi001-A (P1L5)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  1930. RCMGi004-A (P6L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  1931. RCMGi005-A (P5L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  1932. RCMGi005-B (P5L5)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  1933. RCMGi006-A (VII_MAK_C)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Normal (average)

  1934. RCMGi008-A (P9L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  1935. RCMGi009-A (P14L1)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Fibrodysplasia ossificans progressiva

  1936. RCMGi013-A (P2L2)

    Russia Research Centre for Medical Genetics (RCMG)
    Disease:

    Cystic fibrosis

  1937. RCPCMi004-A (Park14-4)

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

    Obsolete_parkinson's disease

  1938. RCPCMi007-A (IPSFF1S)

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

    Normal (average)

  1939. RCPCMi007-A-1 (IPSFF1S deltab2m)

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

    Normal (average)

  1940. RCPCMi012-A (CYFIP-MV-9R)

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

    West syndrome

  1941. RCPCMi013-A (IPSAVE2S)

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

    Normal (average)

  1942. RCSIi002-A (iDFU8)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Obsolete_diabetes mellitus

  1943. RCSIi003-A (iNFF12)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Normal (average)

  1944. RCSIi004-A (iNFF14)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Normal (average)

  1945. RCSIi005-A (iDFF24)

    Ireland Royal College of Surgeons in Ireland (RCSI)
    Disease:

    Obsolete_diabetes mellitus

  1946. REGi001-A (LEB_M)

    France SAFE iPS Facility (REG)
    Disease:

    Bosch-boonstra-schaaf optic atrophy syndrome

  1947. REGi002-A (CHAP_P)

    France SAFE iPS Facility (REG)
    Disease:

    Bosch-boonstra-schaaf optic atrophy syndrome

  1948. REGi004-A (MAR_N)

    France SAFE iPS Facility (REG)
    Disease:

    Bosch-boonstra-schaaf optic atrophy syndrome

  1949. REGi007-A (COL_T)

    France SAFE iPS Facility (REG)
    Disease:

    Bosch-boonstra-schaaf optic atrophy syndrome

  1950. REGUi001-A (IPS4FLV)

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

    Normal (average)

  1951. REGUi017-A (4F_Tie2_RNA191)

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

    Normal (average)

  1952. REGUi017-C (4F_Tie2_Sv191)

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

    Normal (average)

  1953. REGUi017-D (4F_PBMC_Sv191)

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

    Normal (average)

  1954. REGUi018-C (4F_Tie2_Sv192)

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

    Normal (average)

  1955. REGUi018-D (4F_PBMC_Sv192)

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

    Normal (average)

  1956. RFSCi001-A (RFSC3)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  1957. RFSCi005-A (RFSC18)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  1958. RFSCi007-A (RFSC10)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  1959. RFSCi008-A (RFSC16)

    United States RETINA FOUNDATION OF THE SOUTHWEST (RFSC)
    Disease:

    Normal (average)

  1960. RGIe013-A (SI-79)

    United States Reproductive Genetics Institute (RGI)

  1961. RGIe111-A (SI-208)

    United States Reproductive Genetics Institute (RGI)

  1962. RGIe151-A (SI-252)

    United States Reproductive Genetics Institute (RGI)
    Disease:

    47,xxx syndrome

  1963. RIi013-A (ARMD.1.H.iPSC.2)

    Iran Royan Institute (RI)
    Disease:

    Obsolete_age-related macular degeneration

  1964. RIe012-B (hE8)

    Iran Royan Institute (RI)
    Disease:

    Normal (average)

  1965. UCSFi001-A-87

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Tuberous sclerosis 2

  1966. RMCGENi020-A (IPS15-00004)

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Stargardt disease

  1967. SCTCi043-A-1 (iPS23-00086 clE2 and fIPS_DM1Rescue_P1 clE2)

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Myotonic dystrophy type 1

  1968. SCTCi044-A-1 (iPS24-00086 clB5 and fiPS_DM1Rescue_P2 clB5)

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Myotonic dystrophy type 1

  1969. SCTCi045-A-1 (iPS24-00085 clE3 and fIPS_DM1Rescue_P3 clE3)

    Netherlands Radboudumc - Department of Human Genetics (RMCGEN)
    Disease:

    Myotonic dystrophy type 1

  1970. RNRMUi001-A (RDEB-iPSC-d1)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Epidermolysis bullosa dystrophica, autosomal recessive

  1971. RNRMUi002-A (RDEB-iPSC-d2)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Epidermolysis bullosa dystrophica, autosomal recessive

  1972. KUIFMSi004-A-1 (hPSC MPP8 Neon Green)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Normal (average)

  1973. RNRMUi005-A (EB-iPSC-d4 and RDEB-iPSC-d4)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Recessive dystrophic epidermolysis bullosa

    Disease:

    Epidermolysis bullosa simplex

  1974. RNRMUi006-A (RDEB-IPSC-d10)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Recessive dystrophic epidermolysis bullosa

  1975. RNRMUi007-A (EBS-iPSC-d12)

    Russia Pirogov Russian National Research Medical University (RNRMU)
    Disease:

    Epidermolysis bullosa simplex 2f, with mottled pigmentation

  1976. RTIBDi001-A (MCND-TENS2)

    United States Regenerative Therapies for Inherited Blood Disorder (RTIBD)
    Disease:

    Normal (average)

  1977. RUCDRi002-A (TC-113, 50-001-21, 50-001-21.P20_10, ND50038, LiPSC-GR1.1 and TC-1133)

    United States RUCDR Infinite Biologics (RUCDR)
    Disease:

    Normal (average)

  1978. SANi013-A (TRACER #P5 clone F)

    Netherlands Sanquin (SAN)
    Disease:

    Diamond-blackfan anemia

  1979. SBWCHi001-A

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

    Ctnnb1 gene mutation

  1980. SCTi003-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  1981. SCTi004-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  1982. SCTi005-A

    United States STEMCELL Technologies Inc. (SCT)
    Disease:

    Normal (average)

  1983. WAe009-A-1X (H9 ALK CRISPR F1174L)

    Canada STEMCELL Technologies Inc. (SCT)
    Disease:

    Neuroblastoma

  1984. SCTCi008-A (IPS17-00095)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  1985. SCTCi010-A (IPS17-00041)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  1986. SCTCi011-A (IPS18-00072)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Obsolete_age-related macular degeneration

  1987. SCTCi012-A (IPS19-00027)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Obsolete_age-related macular degeneration

  1988. SCTCi013-A (IPS19-00053)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Obsolete_age-related macular degeneration

  1989. SCTCi014-A (IPS17-00056)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Age-related macular degeneration

  1990. SCTCi020-A (IPS17-00028)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Normal (average)

  1991. SCTCi022-A (IPS17-00042)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  1992. SCTCi023-A (IPS17-00063)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Self-limited familial neonatal epilepsy

  1993. SCTCi024-A (IPS18-00047)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  1994. SCTCi025-A (IPS18-00095)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Self-limited familial neonatal epilepsy

  1995. SCTCi028-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Pyridoxine-dependent epilepsy

  1996. SCTCi030-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Glutaric acidemia type 1

  1997. SCTCi031-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Glutaric acidemia type 1

  1998. SCTCi032-A

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Glutaric acidemia type 1

  1999. SCTCi037-A (IPS19-00015)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  2000. SCTCi039-A (IPS19-00092)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Developmental and epileptic encephalopathy, 7

  2001. SCTCi043-A (fIPS_DM1_P1 cl1 and iPS19-00072 cl1)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Myotonic dystrophy type 1

  2002. SCTCi044-A (fIPS_DM1_P2 cl1 and iPS19-00073 cl1)

    Netherlands Radboudumc Stem Cell Technology Center (SCTC)
    Disease:

    Myotonic dystrophy type 1

  2003. SCVIi030-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  2004. SCVIi053-A (2021)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Normal (average)

  2005. SCVIi059-A (SCVIi2413)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  2006. SCVIi062-A (SCVI2150c1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome

  2007. SCVIi074-A (SCVIi599C1)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Hypertrophic cardiomyopathy

  2008. SCVIi078-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Catecholaminergic polymorphic ventricular tachycardia

  2009. SCVIi079-A (SCVI167 and PHBI-ST-036)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Idiopathic pulmonary hypertension

  2010. SCVIi081-A (SCVI2535)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  2011. SCVIi083-A (SCVI2655)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Breast cancer

  2012. SCVIi085-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Obsolete_down syndrome

  2013. SCVIi086-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Obsolete_down syndrome

  2014. SCVIi088-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Duchenne muscular dystrophy

  2015. SCVIi092-A (SCVI2628)

    United States Stanford Cardiovascular Institute (SCVI)

  2016. SCVIi108-A (SCVI2767)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Familial hypercholesterolemia

  2017. SCVIi110-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Long qt syndrome 1

  2018. SCVIi115-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Lynch syndrome

  2019. SCVIi123-A (SCVI 2176)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  2020. SCVIi129-A (SCVI2454)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Marfan syndrome

  2021. SCVIi132-A

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  2022. SCVIi137-A (SCVI 770)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Myotonic dystrophy type 1

  2023. SCVIi139-A (SCVI2925)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Thoracic aortic aneurysm

  2024. SCVIi158-A (SCVI2930)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  2025. SCVIi159-A (SCVI3070)

    United States Stanford Cardiovascular Institute (SCVI)
    Disease:

    Dilated cardiomyopathy

  2026. SDCHi001-A

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Normal (average)

  2027. SDCHi005-A (DEPDC5-ZHW)

    China Children's Hospital Affiliated to Shandong University (SDCH)
    Disease:

    Epilepsy

  2028. SDPHi006-A

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

    Normal (average)

  2029. SDPHi007-A

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

    Alagille syndrome

  2030. SDQLCHi028-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Xia-gibbs syndrome

  2031. SDQLCHi050-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Normal (average)

  2032. SDQLCHi061-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Carbamoyl phosphate synthetase i deficiency disease

  2033. SDQLCHi063-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Maturity-onset diabetes of the young type 2

  2034. SDQLCHi064-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Canavan disease

  2035. SDQLCHi065-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Down syndrome

  2036. SDQLCHi067-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Subcortical band heterotopia

  2037. SDQLCHi068-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Immunodeficiency 14a, autosomal dominant

  2038. SDQLCHi073-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Cockayne syndrome

  2039. SDQLCHi080-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Gm1 gangliosidosis

  2040. SDQLCHi081-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Rahman syndrome

  2041. SDQLCHi087-A

    China Children’s Hospital affiliated to Shandong University (SDQLCH)
    Disease:

    Normal (average)

  2042. SDUe001-A (Odense3)

    Denmark University of Southern Denmark (SDU)

  2043. SDUe002-A (KMEB1)

    Denmark University of Southern Denmark (SDU)

  2044. SHCDNi001-A (SHCDN001)

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Mitochondrial dna depletion syndrome

  2045. SHCDNi007-A

    China Shanghai Children's Hospital (SHCDN)
    Disease:

    Pyruvate carboxylase deficiency

  2046. SHCDNRi001-A (IPS-51)

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

    Alport syndrome

  2047. SHCHNDi002-A

    China Shanghai Children's Hospital (SHCHND)
    Disease:

    Infantile liver failure syndrome 2

  2048. SHEHi002-A (iPS36)

    China Shanghai East Hospital (SHEH)
    Disease:

    Long qt syndrome 8

  2049. SHEHDNi002-A (KY03AP)

    China Department of Neurology (SHEHDN)
    Disease:

    Parkinson disease

  2050. SHFDi001-A (SHFD-1)

    China Shanghai Stomatological Hospital, Fudan University, Shanghai, China (SHFD)
    Disease:

    Ankylosing spondylitis

  2051. SIAISi004-A (ZYF)

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

    Obsolete_alzheimer's disease

  2052. SIAISi007-A (ZSJ)

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

    Alzheimer's disease

  2053. SIAISi008-A (ZMY)

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

    Obsolete_alzheimer's disease

  2054. SIAISi011-A (NZM)

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

    Normal (average)

  2055. SIAISi019-A

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

    Normal (average)

  2056. SIAISi020-A

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

    Mild cognitive impairment

  2057. SIGi001-A-1 (iPSC0028 SLC17A7/GFP E3)

    United States Sigma-Aldrich (SIG)
    Disease:

    Normal (average)

  2058. SIGi001-A-2 (iPSC0028 SLC17A7/GFP C3)

    United States Sigma-Aldrich (SIG)
    Disease:

    Normal (average)

  2059. SIGi001-A-3 (iPSC0028 MAPT P301L C4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  2060. SIGi001-A-4 (iPSC0028 MAPT P301L D4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  2061. SIGi001-A-5 (iPSC0028 MAPT P301S 1C9C4)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  2062. SIGi001-A-7 (iPSC0028 MAPT P301S 2G2B7)

    United States Sigma-Aldrich (SIG)
    Disease:

    Frontotemporal dementia

  2063. SIGi001-A-8 (iPSC0028 MAPT P301S+Ex10+16/Clone 7D11A7)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  2064. SIGi001-A-10 (iPSC0028 MAPT P301S+Ex10+16/Clone 7G4A8)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  2065. SIGi001-A-11 (iPSC0028 MAPT P301S+Ex10+16/Clone 7C6A4 and SAMEA4451118)

    United States Sigma-Aldrich (SIG)
    Disease:

    Progressive supranuclear palsy

    Disease:

    Corticobasal degeneration disorder

  2066. SIGi001-A-13 (iPSC0028 – MonoAllelic MAPT_Ex10+16T/Clone 1D01-11)

    United States Sigma-Aldrich (SIG)
    Disease:

    Alzheimer disease

  2067. SJTUGHi001-A

    China Shanghai General Hospital (SJTUGH)
    Disease:

    Retinitis pigmentosa

  2068. SJTUGHi002-A

    China Shanghai General Hospital (SJTUGH)
    Disease:

    Retinitis pigmentosa

  2069. SJTUXHi003-A

    China Shanghai Xinhua Hospital (SJTUXH)
    Disease:

    Familial exudative vitreoretinopathy

  2070. SKLOi004-B

    China State Key Laboratory of Ophthalmology (SKLO)
    Disease:

    Retinoblastoma

  2071. SKLOi005-B

    China State Key Laboratory of Ophthalmology (SKLO)
    Disease:

    Leber congenital amaurosis

  2072. SKLRMi001-A

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

    Androgen insensitivity syndrome

  2073. SKLRMe011-A

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

    Rett syndrome

  2074. SMBCi009-A

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Obsolete_familial hypercholesterolemia

  2075. SMBCi013-A (WD-iPSC)

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Hepatolenticular degeneration

  2076. SMBCi022-A (5003)

    China Shandong Medicinal Biotechnology Center (SMBC)
    Disease:

    Fabry disease

  2077. WAe009-A-3F

    China Southern Medical University (SMUDH)
    Disease:

    Normal (average)

  2078. SMUSHi006-A

    China Southern Medical University Shenzhen hospital (SMUSH)
    Disease:

    Amyotrophic lateral sclerosis

  2079. SNUe003-A (SNUhES3)

    South Korea Seoul National University (SNU)
    Disease:

    Normal (average)

  2080. SNUe004-A (SNUhES4)

    South Korea Seoul National University (SNU)
    Disease:

    Normal (average)

  2081. SNUHBBi002-A (SNUHBB2112_iPSC_C1)

    South Korea Seoul National University Hospital Dementia Brain Bank (SNUHBB)
    Disease:

    Alzheimer's disease

  2082. SPHi001-A (SLEi002HZY)

    China Shenzhen People's Hospital (SPH)
    Disease:

    Systemic lupus erythematosus

  2083. WAe009-A-74

    China Shenzhen People's Hospital (SPH)
    Disease:

    Long qt syndrome 2

  2084. WAe009-A-88

    China Shenzhen People's Hospital (SPH)
    Disease:

    Long qt syndrome 2

  2085. SSCCe003-A (ESI-017)

    Singapore Singapore Stem Cell Consortium (SSCC)

  2086. SSMCi001-A

    China The Fourth People's Hospital of Shenzhen (Shenzhen Samii Medical Center) (SSMC)
    Disease:

    Dilated cardiomyopathy

  2087. STBCi004-A (SFC832-03-19)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2088. STBCi004-B (SFC832-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2089. STBCi004-C (SFC832-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2090. STBCi005-C (SFC833-03-14)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2091. STBCi006-A (SFC140-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2092. STBCi007-A (SFC855-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2093. STBCi007-C (SFC855-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2094. STBCi010-A (SFC802-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2095. STBCi011-C (SFC803-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2096. STBCi013-A (SFC807-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2097. STBCi013-B (SFC807-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2098. STBCi014-C (SFC808-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2099. STBCi015-C (SFC809-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2100. STBCi019-C (SFC828-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2101. STBCi024-C (SFC831-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2102. STBCi025-B (SFC834-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2103. STBCi027-A (SFC017-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2104. STBCi027-B (SFC017-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2105. STBCi028-A (SFC018-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2106. STBCi028-B (SFC018-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2107. STBCi028-C (SFC018-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2108. STBCi029-A (SFC020-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2109. STBCi029-B (SFC020-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2110. STBCi030-A (SFC023-03-24)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2111. STBCi030-B (SFC023-03-43)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2112. STBCi031-A (SFC024-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2113. STBCi031-B (SFC024-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2114. STBCi031-C (SFC024-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2115. STBCi032-A (SFC042-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2116. STBCi032-B (SFC042-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2117. STBCi033-A (SFC084-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2118. STBCi033-B (SFC084-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2119. STBCi033-C (SFC084-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2120. STBCi034-A (SFC091-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2121. STBCi034-B (SFC091-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2122. STBCi035-B (SFC813-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2123. STBCi035-C (SFC813-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2124. STBCi037-B (SFC816-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2125. STBCi037-C (SFC816-03-13)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2126. STBCi038-A (SFC011-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2127. STBCi038-B (SFC011-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2128. STBCi038-C (SFC011-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2129. STBCi039-A (SFC062-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2130. STBCi039-B (SFC062-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2131. STBCi039-C (SFC062-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2132. STBCi040-A (SFC029-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2133. STBCi040-B (SFC029-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2134. STBCi040-C (SFC029-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2135. STBCi041-A (SFC081-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2136. STBCi041-B (SFC081-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2137. STBCi041-C (SFC081-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2138. STBCi043-A (SFC120-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2139. STBCi043-B (SFC120-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2140. STBCi043-C (SFC120-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2141. STBCi044-B (SFC841-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2142. STBCi045-A (SFC039-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2143. STBCi045-B (SFC039-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2144. STBCi045-C (SFC039-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2145. STBCi046-A (SFC021-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2146. STBCi046-B (SFC021-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2147. STBCi047-A (SFC043-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2148. STBCi047-B (SFC043-03-13)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2149. STBCi048-A (SFC014-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2150. STBCi048-B (SFC014-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2151. STBCi048-C (SFC014-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2152. STBCi049-A (SFC040-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2153. STBCi049-B (SFC040-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2154. STBCi049-C (SFC040-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2155. STBCi050-A (SFC041-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2156. STBCi050-B (SFC041-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2157. STBCi050-C (SFC041-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2158. STBCi051-A (SFC056-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2159. STBCi051-B (SFC056-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2160. STBCi051-C (SFC056-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2161. STBCi052-A (SFC086-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2162. STBCi052-B (SFC086-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2163. STBCi052-C (SFC086-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2164. STBCi053-A (SFC089-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2165. STBCi053-B (SFC089-03-55)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2166. STBCi053-C (SFC089-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2167. STBCi054-A (SFC010-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2168. STBCi054-B (SFC010-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2169. STBCi055-A (SFC026-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2170. STBCi055-B (SFC026-04-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2171. STBCi055-C (SFC026-04-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2172. STBCi056-A (SFC064-03-39)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2173. STBCi056-B (SFC064-03-42)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2174. STBCi056-C (SFC064-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2175. STBCi057-A (SFC065-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2176. STBCi057-B (SFC065-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2177. STBCi057-C (SFC065-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2178. STBCi058-A (SFC012-04-20)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2179. STBCi058-B (SFC012-04-30)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2180. STBCi058-C (SFC012-04-31)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2181. STBCi059-A (SFC015-01-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2182. STBCi059-B (SFC015-01-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2183. STBCi059-C (SFC015-01-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2184. STBCi060-A (SFC038-07-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2185. STBCi060-B (SFC038-07-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2186. STBCi060-C (SFC038-07-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2187. STBCi061-A (SFC850-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2188. STBCi062-A (SFC851-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2189. STBCi063-A (SFC856-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2190. STBCi063-B (SFC856-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2191. STBCi063-C (SFC856-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2192. STBCi064-A (SFC180-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2193. STBCi065-A (SFC853-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2194. STBCi066-A (SFC854-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2195. STBCi067-A (SFC855-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2196. STBCi068-A (SFC035-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2197. STBCi068-B (SFC035-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2198. STBCi068-C (SFC035-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2199. STBCi069-A (SFC050-03-21)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2200. STBCi069-B (SFC050-03-22)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2201. STBCi069-C (SFC050-03-20)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2202. STBCi070-A (SFC052-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2203. STBCi070-B (SFC052-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2204. STBCi071-A (SFC057-07-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2205. STBCi071-B (SFC057-07-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2206. STBCi071-C (SFC057-07-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2207. STBCi072-A (SFC058-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2208. STBCi072-B (SFC058-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2209. STBCi072-C (SFC058-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2210. STBCi073-A (SFC106-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2211. STBCi073-B (SFC106-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2212. STBCi074-A (SFC109-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2213. STBCi074-B (SFC109-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2214. STBCi074-C (SFC109-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2215. STBCi075-A (SFC129-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2216. STBCi075-B (SFC129-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2217. STBCi075-C (SFC129-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2218. STBCi076-A (SFC134-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2219. STBCi077-A (SFC136-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2220. STBCi077-B (SFC136-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2221. STBCi077-C (SFC136-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2222. STBCi078-A (SFC013-07-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2223. STBCi078-B (SFC013-07-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2224. STBCi078-C (SFC013-07-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2225. STBCi079-A (SFC045-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2226. STBCi079-B (SFC045-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2227. STBCi079-C (SFC045-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2228. STBCi080-A (SFC047-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2229. STBCi080-B (SFC047-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2230. STBCi080-C (SFC047-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2231. STBCi081-A (SFC170-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2232. STBCi081-B (SFC170-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2233. STBCi081-C (SFC170-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2234. STBCi082-A (SFC888-07-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2235. STBCi082-B (SFC888-07-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2236. STBCi082-C (SFC888-07-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2237. STBCi083-A (SFC830-04-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2238. STBCi083-B (SFC830-04-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2239. STBCi084-A (SFC871-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2240. STBCi084-B (SFC871-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2241. STBCi084-C (SFC871-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2242. STBCi085-A (SFC866-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2243. STBCi085-B (SFC866-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2244. STBCi085-C (SFC866-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2245. STBCi086-A (SFC842-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2246. STBCi086-B (SFC842-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2247. STBCi087-A (SFC845-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2248. STBCi087-B (SFC845-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2249. STBCi087-C (SFC845-03-11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2250. STBCi088-A (SFC872-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2251. STBCi088-B (SFC872-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2252. STBCi088-C (SFC872-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2253. STBCi089-C (SFC868-03-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2254. STBCi090-B (SFC867-04-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2255. STBCi091-A (SFC126-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2256. STBCi091-B (SFC126-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2257. STBCi091-C (SFC126-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2258. STBCi092-A (SFC049-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2259. STBCi092-B (SFC049-03-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2260. STBCi092-C (SFC049-03-13)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2261. STBCi093-B (SFC893-07-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2262. STBCi094-A (BPC321-01-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_drug-induced liver injury

  2263. STBCi094-B (BPC321-01-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_drug-induced liver injury

  2264. STBCi094-C (BPC321-01-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_drug-induced liver injury

  2265. STBCi095-A (BPC339-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_drug-induced liver injury

  2266. STBCi096-A (BPC340-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Congenital long qt syndrome

  2267. STBCi097-A (SFC055-04-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2268. STBCi097-B (SFC055-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2269. STBCi097-C (SFC055-04-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2270. STBCi098-A (SFC048-07-14)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  2271. STBCi098-B (SFC048-07-18)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  2272. STBCi098-C (SFC048-07-17)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  2273. STBCi099-A (SFC059-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2274. STBCi099-B (SFC059-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2275. STBCi100-A (SFC117-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  2276. STBCi101-A (SFC156-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2277. STBCi102-A (SFC163-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2278. STBCi103-A (SFC294-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2279. STBCi105-A (SFC067-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2280. STBCi106-A (SFC068-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2281. STBCi107-A (SFC104-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  2282. STBCi108-A (SFC110-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2283. STBCi109-A (SFC113-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2284. STBCi110-A (SFC116-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

    Disease:

    Age-related macular degeneration

  2285. STBCi111-A (SFC131-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2286. STBCi112-A (SFC177-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2287. STBCi113-A (SFC178-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2288. STBCi114-A (SFC034-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2289. STBCi115-A (SFC162-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2290. STBCi116-A (SFC164-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2291. STBCi117-A (SFC246-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2292. STBCi118-A (SFC037-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2293. STBCi119-A (SFC044-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2294. STBCi120-A (SFC046-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2295. STBCi121-A (SFC112-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2296. STBCi122-A (SFC115-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  2297. STBCi123-A (SFC053-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2298. STBCi124-A (SFC135-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2299. STBCi125-A (SFC175-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2300. STBCi126-A (SFC105-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  2301. STBCi127-A (SFC107-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Type 2 diabetes mellitus

  2302. STBCi128-A (SFC108-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2303. STBCi129-A (SFC137-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2304. STBCi130-A (SFC172-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2305. STBCi131-A (SFC295-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2306. STBCi132-A (SFC301-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2307. STBCi133-A (SFC302-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2308. STBCi134-A (SFC019-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2309. STBCi135-A (SFC033-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2310. STBCi136-A (SFC036-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2311. STBCi137-A (SFC076-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2312. STBCi138-A (SFC079-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2313. STBCi139-A (SFC101-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2314. STBCi140-A (SFC102-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2315. STBCi141-A (SFC103-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2316. STBCi142-A (SFC118-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2317. STBCi143-A (SFC122-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2318. STBCi144-A (SFC123-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2319. STBCi145-A (SFC125-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2320. STBCi146-A (SFC127-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2321. STBCi147-A (SFC128-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2322. STBCi148-A (SFC130-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2323. STBCi149-A (SFC132-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2324. STBCi150-A (SFC133-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2325. STBCi151-A (SFC145-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2326. STBCi152-A (SFC146-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2327. STBCi153-A (SFC147-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2328. STBCi154-A (SFC148-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2329. STBCi155-A (SFC149-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2330. STBCi156-A (SFC150-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2331. STBCi157-A (SFC154-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2332. STBCi158-A (SFC155-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2333. STBCi159-A (SFC158-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2334. STBCi160-A (SFC159-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2335. STBCi161-A (SFC160-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2336. STBCi162-A (SFC161-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2337. STBCi163-A (SFC165-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2338. STBCi164-A (SFC166-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2339. STBCi165-A (SFC168-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2340. STBCi166-A (SFC169-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2341. STBCi167-A (SFC174-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2342. STBCi168-A (SFC176-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2343. STBCi169-A (SFC179-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2344. STBCi170-A (SFC190-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2345. STBCi171-A (SFC191-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2346. STBCi172-A (SFC192-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2347. STBCi173-A (SFC193-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2348. STBCi174-A (SFC194-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2349. STBCi175-A (SFC195-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2350. STBCi176-A (SFC196-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2351. STBCi177-A (SFC197-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2352. STBCi178-A (SFC198-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2353. STBCi179-A (SFC243-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2354. STBCi180-A (SFC242-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2355. STBCi181-A (SFC247-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2356. STBCi182-A (SFC248-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2357. STBCi183-A (SFC250-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2358. STBCi184-A (SFC251-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2359. STBCi185-A (SFC253-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2360. STBCi186-A (SFC255-03-01 and SFC255-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2361. STBCi187-A (SFC256-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2362. STBCi188-A (SFC257-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2363. STBCi189-A (SFC258-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2364. STBCi190-A (SFC259-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2365. STBCi191-A (SFC260-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2366. STBCi192-A (SFC261-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2367. STBCi193-A (SFC262-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2368. STBCi194-A (SFC263-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2369. STBCi195-A (SFC286-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2370. STBCi196-A (SFC287-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2371. STBCi197-A (SFC288-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2372. STBCi198-A (SFC289-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2373. STBCi199-A (SFC290-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2374. STBCi200-A (SFC291-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2375. STBCi201-A (SFC292-03-02 and SFC292-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2376. STBCi202-A (SFC293-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2377. STBCi203-A (SFC296-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2378. STBCi204-A (SFC297-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2379. STBCi205-A (SFC298-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2380. STBCi206-A (SFC299-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2381. STBCi207-A (SFC300-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2382. STBCi208-A (SFC303-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2383. STBCi209-A (SFC304-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2384. STBCi210-A (SFC305-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2385. STBCi211-A (SFC306-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2386. STBCi212-A (SFC312-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2387. STBCi213-A (SFC313-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2388. STBCi214-A (SFC314-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2389. STBCi215-A (SFC318-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2390. STBCi216-A (SFC319-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2391. STBCi217-A (SFC320-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2392. STBCi218-A (SFC357-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2393. STBCi219-A (SFC358-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2394. STBCi220-A (SFC359-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2395. STBCi221-A (SFC360-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2396. STBCi222-A (SFC361-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2397. STBCi223-A (SFC363-04-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2398. STBCi224-A (SFC364-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2399. STBCi225-A (SFC365-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2400. STBCi226-A (SFC366-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2401. STBCi227-A (SFC367-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2402. STBCi228-A (SFC368-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2403. STBCi229-A (SFC369-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2404. STBCi230-A (SFC372-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2405. STBCi231-A (SFC374-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2406. STBCi232-A (SFC375-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Neuropathy

  2407. STBCi248-A (SFC999-01-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Normal (average)

  2408. STBCi249-A (SFC171-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Bipolar disorder

  2409. STBCi252-A (SFC254-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2410. STBCi253-A (SFC184-01-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2411. STBCi254-A (SFC143-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2412. STBCi255-A (SFC183-01-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2413. STBCi256-A (SFC144-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2414. STBCi257-A (SFC185-01-11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2415. STBCi258-A (SFC090-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2416. STBCi259-A (SFC032-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2417. STBCi260-A (SFC279-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2418. STBCi261-A (SFC186-01-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2419. STBCi262-A (SFC271-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2420. STBCi263-A (SFC268-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2421. STBCi264-A (SFC142-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2422. STBCi265-A (SFC121-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2423. STBCi266-A (SFC072-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2424. STBCi267-A (SFC027-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2425. STBCi268-A (SFC077-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2426. STBCi269-A (BPC943-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2427. STBCi270-A (BPC944-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2428. STBCi271-A (BPC936-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2429. STBCi272-A (BPC930-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2430. STBCi273-A (BPC928-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2431. STBCi274-A (BPC935-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2432. STBCi275-A (BPC937-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2433. STBCi276-A (BPC933-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2434. STBCi277-A (BPC934-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2435. STBCi278-A (SFC245-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2436. STBCi279-A (SFC063-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2437. STBCi280-A (SFC066-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2438. STBCi281-A (SFC167-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2439. STBCi282-A (SFC138-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2440. STBCi283-A (SFC073-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2441. STBCi284-A (BPC939-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2442. STBCi285-A (BPC940-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2443. STBCi286-A (BPC929-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2444. STBCi287-A (BPC946-04-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2445. STBCi288-A (SFC028-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2446. STBCi289-A (SFC030-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2447. STBCi290-A (SFC069-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2448. STBCi291-A (SFC080-03-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2449. STBCi292-A (SFC139-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2450. STBCi293-A (SFC843-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2451. STBCi297-A (SFC061-03-07)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2452. STBCi299-A (BPC931-01-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2453. STBCi300-A (BPC932-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2454. STBCi301-A (BPC949-04-11)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2455. STBCi302-A (BPC945-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2456. STBCi303-A (SFC071-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2457. STBCi304-A (SFC074-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2458. STBCi305-A (SFC083-03-10 and SFC083-07-10)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2459. STBCi306-A (SFC087-03-04 and SFC087-07-04)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2460. STBCi307-A (SFC088-03-05)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2461. STBCi308-A (SFC249-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2462. STBCi309-A (SFC391-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2463. STBCi310-A (SFC846-03-02)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2464. STBCi311-A (BPC941-03-12)

    United Kingdom StemBANCC (STBC)
    Disease:

    Migraine disorder

  2465. STBCi312-A (BPC333-03-09)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2466. STBCi313-A (BPC334-03-06)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2467. STBCi314-A (BPC335-03-08)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2468. STBCi315-A (BPC336-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Alzheimer disease

  2469. STBCi316-A (SFC244-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2470. STBCi317-A (SFC241-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2471. STBCi318-A (SFC200-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2472. STBCi319-A (SFC199-03-01)

    United Kingdom StemBANCC (STBC)
    Disease:

    Obsolete_diabetes mellitus

  2473. STBCi320-A (SFC031-03-03)

    United Kingdom StemBANCC (STBC)
    Disease:

    Parkinson disease

  2474. STJUDEi004-A (INS3)

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

    Diamond-blackfan anemia

  2475. SUHi001-A (RES143 and Cell line 1 143)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  2476. SUHi003-A (RES146 and Cell line 3 146)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  2477. SUHi009-A (RES105 and Cell line 12 105:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Normal (average)

  2478. SUHi011-A (RES151 and Cell line 13 151)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Asthma

  2479. SUHi013-A (RES110 and Cell line 11 110:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  2480. SUHi016-A (RES142 and Cell line 16 142:3)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  2481. SUHi017-A (RES158 and Cell line 24 158)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Breast carcinoma

  2482. SUHi020-A (RES114 and Cell line 19 114:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  2483. SUHi021-A (RES116 and Cell line 20 116:5)

    Sweden Sahlgrenska University Hospital (SUH)
    Disease:

    Obesity

  2484. SUSMi001-A (RY3)

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

    Pelizaeus-merzbacher disease

  2485. UCSFi001-A-65

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

    Obsolete_dilated cardiomyopathy

  2486. SUSMi002-A (02-005)

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

    Pelizaeus-merzbacher disease

  2487. SUSMi005-A-1 (SNCA3X 0KO C1 and SNCA3X 0KO C2)

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

    Obsolete_parkinson's disease

  2488. SXMUi002-A (SXMUi001-A-1 and F8-iPSC)

    China Shanxi Medical University (SXMU)
    Disease:

    Hemophilia a

  2489. SYSUi005-A

    China Sun Yat-sen University (SYSU)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  2490. WAe009-A-71

    China Sun Yat-sen University (SYSU)
    Disease:

    Waardenburg syndrome type 4c

  2491. WAe009-A-81 (H9-MSX1-/- cell line)

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

    Tooth agenesis

  2492. SYSUTFi001-A

    China The First Affiliated Hospital (SYSUTF)
    Disease:

    Hepatocellular carcinoma

  2493. SZBKi002-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  2494. SZBKi002-B

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  2495. SZBKi003-A

    China Shenzhen Beike Biotechnology Co., Ltd. (SZBK)
    Disease:

    Normal (average)

  2496. SZGJMSi001-A (ZLP-2)

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

    Schizophrenia

  2497. TAUi001-A (UTA.09703.HCMJp)

    Finland Tampere University (TAU)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  2498. TAUi002-A (UTA.04602.WT)

    Finland Tampere University (TAU)
    Disease:

    Normal (average)

  2499. TAUi003-A (UTA.11505.WTsb)

    Finland Tampere University (TAU)
    Disease:

    Normal (average)

  2500. TAUi006-A (UTA.00102.LQT1)

    Finland Tampere University (TAU)
    Disease:

    Long qt syndrome 1

  2501. TAUi007-B (UTA.00211.LQT1)

    Finland Tampere University (TAU)
    Disease:

    Long qt syndrome 1

  2502. TCGINKi003-A (INK-iCON-004)

    India CHINTA (TCGINK)
    Disease:

    Normal (average)

  2503. TCIERi001-A (IER-EK1)

    Taiwan Institute of Eye Research, Hualien Tzu Chi Hospital (TCIER)
    Disease:

    Normal (average)

  2504. TISSUi001-A (HUMIMIC101, StemUse101 and SU101)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  2505. TISSUi003-A (HUMIMIC103, StemUse103, SU103)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  2506. TISSUi005-A (HUMIMIC105, StemUse105, SU105)

    Germany TissUse GmbH (TISSU)
    Disease:

    Leukemia

  2507. TISSUi006-A (HUMIMIC106, StemUse106 and SU106)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  2508. TISSUi007-A (HUMIMIC107, StemUse107 and SU107)

    Germany TissUse GmbH (TISSU)
    Disease:

    Normal (average)

  2509. TMPi008-A (MR-013 c3 and MR013 c3)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  2510. TMPi009-B (MR014 c27 and MR-014 c27)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  2511. TMPi010-A (K013 c20 and KO-013 c20)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Normal (average)

  2512. TMPi012-A (MR-023 c17 and MR023 c17)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  2513. TMPi013-A (MR-012 and MR012)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  2514. TMPi013-B (MR-012 c12 and MR012 c12)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  2515. TMPi014-A (MR030 c1 and MR-030 c1)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  2516. TMPi014-B (MR030 c2 and MR-030 c2)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  2517. TMPi016-A (NR003 c6 and NR-003 c6)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  2518. TMPi016-B (NR003 c9 and NR-003 c9)

    Switzerland Translational Molecular Psychiatry (TMP)
    Disease:

    Attention deficit hyperactivity disorder

  2519. TRDSi004-A (TRDS-Cardio-012)

    Israel Technion Research and Development Foundation (TRDS)
    Disease:

    Long qt syndrome 2

  2520. TRNDi032-A (HT977A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Alagille syndrome

  2521. TRNDi033-A (HT1001-B)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Normal (average)

  2522. TRNDi037-A (HT976A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Alagille syndrome

  2523. TRNDi038-A (HT978A)

    United States NIH/NCATS-TRND Branch (TRND)
    Disease:

    Alagille syndrome

  2524. TUSMi003-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  2525. TUSMi006-A (15M0014)

    China Tongji University School of Medicine (TUSM)
    Disease:

    Obsolete_alzheimer's disease

  2526. TUSMi008-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Alzheimer's disease

  2527. TUSMi013-A

    China Tongji University School of Medicine (TUSM)
    Disease:

    Parkinson disease

  2528. UALGi003-B (BUB1P2-iPSC Cl2)

    Portugal Universidade do Algarve (UALG)

  2529. UBi001-A-1

    Spain University of Barcelona (UB)
    Disease:

    Sanfilippo syndrome type c

  2530. UBGi001-A

    China uBriGene (Suzhou) Biosciences Co., Ltd. (UBG)
    Disease:

    Normal (average)

  2531. UBTi001-A (PEB-AL#6)

    Austria Medical University of Graz (UBT)
    Disease:

    Normal (average)

  2532. UCLi002-A (HHItC9D-V34 and DN19)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  2533. UCLi003-A (TSM(exon10+16)V97)

    United Kingdom University College London (UCL)
    Disease:

    Frontotemporal dementia

  2534. UCLi004-A (RCi173 and RCFB60c6)

    United Kingdom University College London (UCL)
    Disease:

    Amyotrophic lateral sclerosis

    Disease:

    Frontotemporal dementia

  2535. UCLi004-C (RCi172 and RCFB60c2)

    United Kingdom University College London (UCL)
    Disease:

    Amyotrophic lateral sclerosis

    Disease:

    Frontotemporal dementia

  2536. UCLi011-A

    United Kingdom University College London (UCL)
    Disease:

    Duchenne muscular dystrophy

  2537. UCLi012-A

    United Kingdom University College London (UCL)
    Disease:

    Duchenne muscular dystrophy

  2538. UCLi021-A (CLN5c.335G>A;619T>C and 484Pb)

    United Kingdom University College London (UCL)
    Disease:

    Cln5

  2539. UCLi022-A (546Pa and CLN5c.1072-1073delTT)

    United Kingdom University College London (UCL)
    Disease:

    Cln5

  2540. UCLi024-A (SMID277 and GOS111B)

    United Kingdom University College London (UCL)
    Disease:

    Argininosuccinic aciduria

  2541. UCSCi001-A (SII-1802)

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

    Amyotrophic lateral sclerosis

  2542. UCSDi001-A-3 (LQT3_4_28_Homo_52_iPSC_P15 and UCSD244i-LQT3-2)

    United States University of California,San Diego (UCSD)
    Disease:

    Long qt syndrome 3

  2543. UCSDi001-A-5 (UCSD246i-CNTL-2 and T036_SNP1_Het_3_iPSC_P16_R01)

    United States University of California,San Diego (UCSD)
    Disease:

    Long qt syndrome 3

  2544. UEFi004-A

    Finland University of Eastern Finland (UEF)
    Disease:

    Cstb wt allele

  2545. UEFi008-A (FTD1)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  2546. UEFi009-A (FTD2)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  2547. UEFi011-A (FTD4)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  2548. UEFi013-A (FTD6)

    Finland University of Eastern Finland (UEF)
    Disease:

    Behavioral variant of frontotemporal dementia

  2549. UGENTi001-A (UGENT-MFS003)

    Belgium Ghent University (UGENT)
    Disease:

    Marfan syndrome

  2550. UGENTi001-A-1 (UGENT-MFS003-CRISPR)

    Belgium Ghent University (UGENT)
    Disease:

    Marfan syndrome

  2551. UGENTi003-A (Clone_1 and EMC379i/c1)

    Belgium Ghent University (UGENT)
    Disease:

    Rod-cone dystrophy

  2552. UGENTi005-B (EMC368i/c2)

    Belgium Ghent University (UGENT)
    Disease:

    Inherited retinal dystrophy

  2553. UGOTSAi006-A (N1-005iC1)

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

    Alzheimer's disease

  2554. UHi004-A (HEL157.1)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  2555. UHi004-B (HEL157.3)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  2556. UHi005-A (HEL158.1)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  2557. UHi005-B (HEL158.2)

    Finland University of Helsinki (UH)
    Disease:

    Obsolete_parkinson's disease

  2558. UHi006-A (HEL24.3)

    Finland University of Helsinki (UH)
    Disease:

    Normal (average)

  2559. UHi007-A (HEL47.2)

    Finland University of Helsinki (UH)
    Disease:

    Normal (average)

  2560. UHe002-A (FES22)

    Finland University of Helsinki (UH)

  2561. UIOi001-A (AG27)

    Norway University of Oslo (UIO)
    Disease:

    Normal (average)

  2562. UJNi001-A

    China University of Jinan (UJN)
    Disease:

    Cornelia de lange syndrome

  2563. UJSi003-A

    China Jiangsu University (UJS)
    Disease:

    Hereditary spastic paraplegia

  2564. UJSi004-A

    China Jiangsu University (UJS)
    Disease:

    Schizophrenia

  2565. UJSi005-A

    China Jiangsu University (UJS)
    Disease:

    Schizophrenia

  2566. UKAi001-A-1 (hsc3_hiPS_11_4 and IRF8-/- iPS1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  2567. UKAi001-B (iPS2 and hsc3_hiPS_29)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  2568. UKAi001-B-1 (hsc3_hiPS_29_23 and IRF8-/- iPS2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  2569. UKAi002-A (PBMNC2_hiPS_007 and PV1 JAK2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  2570. UKAi002-B (PBMNC2_hiPS_009 and PV1 JAK2 V617F het)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  2571. UKAi003-A-2 (PV2 JAK2)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Polycythemia vera

  2572. UKAi004-A (P4_wt4 and patient 1 control 1)

    Germany Universitätsklinikum Aachen (UKA)
    Disease:

    Systemic mastocytosis

  2573. UKBi001-B

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Machado-joseph disease

  2574. UKBi006-A (iLB-C-35m-r1 and LB-35-1)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  2575. UKBi007-A (LB-33-5 and iLB-MJD3-33f-r5)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Machado-joseph disease

  2576. UKBi011-A (iLB-AD-169bm-s24)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Alzheimer disease

  2577. UKBi012-A (iLB-C-108bf-s3)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  2578. UKBi013-A (iLB-C-133bm-s4)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  2579. UKBi014-A (A-257s2)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Walker-warburg syndrome

  2580. UKBi015-A-7 (iLB-C16bm-s6 edit BAG3 E10)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  2581. UKBi015-B (iLB-C16bm-s16)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  2582. UKBi015-B-1 (iLB-C16bm-s16 edit DNMT3A KO E11)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Clonal hematopoiesis of indeterminate potential

  2583. UKBi017-A (iLB-C14m-s11)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  2584. UKBi018-A (iLB-C-106bf-s8)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  2585. UKBi020-A (iLB-C-105bm-s4)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Normal (average)

  2586. UKBi022-A (iLB-BAG3-301bm-s2)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  2587. UKBi022-A-1 (iLB-BAG3-301bm-s2 BAG3 edit)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  2588. UKBi023-A (iLB-BAG3-P209L-313bm-s9)

    Germany Universitätsklinikum Bonn (UKB)
    Disease:

    Myofibrillar myopathy 6

  2589. UKEi001-A (ERC001sv1162)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  2590. UKEi001-A-3 (NRAP-OE)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Cardiomyopathy

  2591. UCSFi001-A-1T (PRKD1-G592R-het)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Congenital heart disease

  2592. UCSFi001-A-1U (PRKD1-G592R-hom)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Congenital heart disease

  2593. UKEi001-B (ERC001sv1352)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  2594. UKEi001-C (ERC001sv1355)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  2595. UKEi002-C (ERC017sv2596)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  2596. UKEi003-B (ERC018sv1590)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  2597. UKEi003-C (ERC018sv1634)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Normal (average)

  2598. UKEi070-A (Het)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  2599. UKEi070-A-1 (Rep 28 and Iso Co)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  2600. UKEi070-A-2 (Bi-allelic mutant and Mut 103)

    Germany University Medical Center Hamburg-Eppendorf (UKE)
    Disease:

    Obsolete_hypertrophic cardiomyopathy

  2601. UKERi003-A (UKERiPX7-R1-001)

    Germany Universitätsklinikum Erlangen (UKER)
    Disease:

    Obsolete_parkinson's disease

  2602. HVRDe006-A-1

    United States Universitätsklinikum Erlangen (UKER)
    Disease:

    Coffin-siris syndrome

  2603. UKHGi001-B (M-PKE (e))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Normal (average)

  2604. UKHGi002-A (F-PKE (2))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Normal (average)

  2605. UKHGi002-B (F-PKE (3))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Normal (average)

  2606. UKHGi003-A (PKE (C))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Obsolete_autism spectrum disorder

    Disease:

    Intellectual disability

  2607. UKHGi003-B (PKE (D))

    Germany Institute of Human Genetics Heidelberg (UKHG)
    Disease:

    Obsolete_autism spectrum disorder

    Disease:

    Intellectual disability

  2608. UKKi016-A (NP0078-10)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2609. UKKi016-B (NP0078-12)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2610. UKKi016-C (NP0078-13)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2611. UKKi017-A (NP0075-8D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2612. UKKi017-B (NP0075-10K)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2613. UKKi017-C (NP0075-11B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2614. UKKi018-A (NP0080-2B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2615. UKKi018-B (NP0080-6A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2616. UKKi018-C (NP0080-8B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2617. UKKi019-A (NP0081-1A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2618. UKKi019-C (NP0081-12C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2619. UKKi020-A (NP0100-4)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  2620. UKKi021-A (NP0105-2)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  2621. UKKi023-A (NP0126-1)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2622. UKKi023-B (NP0126-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2623. UKKi023-C (NP0126-6)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2624. UKKi024-A (NP0133-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  2625. UKKi025-A (NP0135-1)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2626. UKKi025-B (NP0135-2)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2627. UKKi025-C (NP0135-7)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2628. UKKi026-A (NP0114-1A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  2629. UKKi027-C (NP0101-C and NP0101-10H)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  2630. UKKi028-A (NP0115-A and NP0115-4)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  2631. UKKi028-B (NP0115-B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  2632. UKKi028-C (NP0115-C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  2633. UKKi029-B (NP0077-16E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2634. UKKi029-C (NP0077-18C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2635. UKKi030-A (NP0134-6D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  2636. UKKi030-B (NP0134-18A)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  2637. UKKi030-C (NP0134-26B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Brugada syndrome

  2638. UKKi031-A (NP0138-8B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2639. UKKi031-B (NP0138-19E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2640. UKKi031-C (NP0138-31B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2641. UKKi032-C (NP0141-31B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  2642. UKKi034-B (NP0079-B and NP0079-15B)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Congenital long qt syndrome

  2643. UKKi035-A (NP0139-A and NP0139-3E)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2644. UKKi035-B (NP0139-B and NP0139-6C)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2645. UKKi035-C (NP0139-C and NP0139-24D)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Rare hypertrophic cardiomyopathy

  2646. UKKi036-A (NP0143-A and NP0143-5)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  2647. UKKi036-B (NP0143-B and NP0143-15)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  2648. UKKi036-C (NP0143-C and NP0143-18)

    Germany Klinikum der Universität zu Köln (UKK)
    Disease:

    Normal (average)

  2649. UKWi008-A (PARK2-9 CL12)

    Germany Universitätsklinikum Würzburg (UKW)
    Disease:

    Attention deficit-hyperactivity disorder

  2650. UKWMPi001-A

    Germany Division of Molecular Psychiatry, Center of Mental Health (UKWMP)
    Disease:

    Normal (average)

  2651. UKWMPi015-A

    Germany Division of Molecular Psychiatry, Center of Mental Health (UKWMP)
    Disease:

    Depression

  2652. UKWMPi017-A

    Germany Division of Molecular Psychiatry, Center of Mental Health (UKWMP)

  2653. UKWMPi019-A

    Germany Division of Molecular Psychiatry, Center of Mental Health (UKWMP)

  2654. UKWNLi007-A (GLA-515G>A-1, GLA-C172Y-iPSC-1 and FD1210/1)

    Germany Neurologische Klinik (UKWNL)
    Disease:

    Fabry disease

  2655. UMi043-A (AD 381852 clone #1)

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

    Alzheimer's disease

  2656. UMi048-A (sord1 GB)

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

    Obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy

  2657. UMi049-A (IIsord1 RV)

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

    Obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy

  2658. UMi053-A (PLS405714 Cl#4)

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

    Primary lateral sclerosis

  2659. UMANi255-A (NB221c)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Foveal hypoplasia

  2660. UMANi255-A-1 (PS02b-B6)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Foveal hypoplasia

  2661. UMANe002-A (Man-13)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Normal (average)

  2662. UMANe004-A (Man-15)

    United Kingdom University of Manchester (UMAN)
    Disease:

    Normal (average)

  2663. UMANCi002-A (TF172D)

    United Kingdom C2T-Kimber lab (UMANC)
    Disease:

    Hnf1b

  2664. UMANe002-A-5 (IBM13-08)

    United Kingdom C2T-Kimber lab (UMANC)
    Disease:

    Normal (average)

  2665. UMCGi002-A (CTP1-C1)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Cardiomyopathy

  2666. UMCGi005-B (PPCM RP2 c9)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Peripartum cardiomyopathy

  2667. UMCGi006-A (DRP1-C2)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  2668. UMCGi008-B (DRP3-C7)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  2669. UMCGi008-C (DRP3-C10)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  2670. UMCGi008-D (DRP3-C11)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Normal (average)

  2671. UMCGi011-C (CTP2-C4)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  2672. UMCGi013-A (UMCG-PD-iPSC-E326K)

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Parkinson disease

  2673. UMCGi016-B

    Netherlands University Medical Center Groningen (UMCG)
    Disease:

    Heart failure

  2674. UMCUi003-A (CRYAB-A527G-91C10)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Dilated cardiomyopathy 1ii

  2675. UMCUi007-A (84C12)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Aortic dissection

  2676. UMCUi008-A (86C6)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Aortic root aneurysm

  2677. UMCUi009-A (87C3)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  2678. UMCUi010-A (88C6)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  2679. UMCUi011-A (119C9)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Aortic root aneurysm

  2680. UMCUi013-A (TNNI3 P1C26)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Restrictive cardiomyopathy

  2681. UMCUi015-A (TNNI3 C1C1)

    Netherlands University Medical Center Utrecht - dept. Heart & Lungs (UMCU)
    Disease:

    Normal (average)

  2682. RUCDRi002-A-74 (Myo-CCER and IPSC-Myo-CCER, LiPSC-GR1.1-Myo-CCER, TC-1133-Myo-CCER)

    Germany University Medical Center Goettingen (UMG)
    Disease:

    Normal (average)

  2683. MHHi001-A-12 (Phx_SRCAP_g3_1200_4)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  2684. MHHi001-A-13 (Phx_SRCAP_g3_1200_7)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  2685. MHHi001-A-14 (Phx_SRCAP_g3_1400_6/8)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities

  2686. MHHi001-A-17 (PHX_CRISPR_JR_DIS13)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities

  2687. UMGWi004-A (BNH1 _iPSC_WT_8)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  2688. UMGWi004-B (BNH1 _iPSC_WT_48)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Normal (average)

  2689. UMGWi004-B-1 (BNH1_iPSC_FHS1_cr_well7_JR)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Floating-harbor syndrome

  2690. UMGWi004-B-2 (BNH1_iPSC_FHS1_cr_well12_JR)

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Floating-harbor syndrome

  2691. UMGWi004-B-3

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Non-syndromic intellectual disability

  2692. UMGWi004-B-4

    Germany Department of Functional Genomics - Human Molecular Genetics (UMGW)
    Disease:

    Non-syndromic intellectual disability

  2693. UMICHi001-A (HVRDi004-B, GM23338 and PGP1 Parental)

    United States University of Michigan (UMICH)
    Disease:

    Normal (average)

  2694. UMICHe001-A (UM134-1 PGD)

    United States University of Michigan (UMICH)

  2695. UMICHe002-A (UM197-1)

    United States University of Michigan (UMICH)
    Disease:

    Spinal and bulbar muscular atrophy, x-linked 1

  2696. UMICHe004-A (UM202-1)

    United States University of Michigan (UMICH)

  2697. UMICHe005-A (UM229-1)

    United States University of Michigan (UMICH)
    Disease:

    Down syndrome

  2698. UMILi004-A (KAB04)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  2699. UMILi005-A (KAB05)

    Italy University of Milan (UMIL)
    Disease:

    Kabuki syndrome

  2700. UMILi013-A (WVS01)

    Italy University of Milan (UMIL)
    Disease:

    Weaver syndrome

  2701. UMILi014-A (WVS04)

    Italy University of Milan (UMIL)
    Disease:

    Weaver syndrome

  2702. UMILi015-A (WVS03)

    Italy University of Milan (UMIL)
    Disease:

    Weaver syndrome

  2703. UMILi028-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  2704. UMILi029-A (SHP1)

    Italy University of Milan (UMIL)
    Disease:

    Autosomal recessive limb-girdle muscular dystrophy-4

  2705. UMILi030-A (SHP2)

    Italy University of Milan (UMIL)
    Disease:

    Autosomal recessive limb-girdle muscular dystrophy-4

  2706. UMILi031-A (SHP3)

    Italy University of Milan (UMIL)
    Disease:

    Autosomal recessive limb-girdle muscular dystrophy-4

  2707. UMILi035-A

    Italy University of Milan (UMIL)
    Disease:

    Congenital central hypoventilation syndrome

  2708. WAe009-A-37 (H9-GSX2-tTA:GFP)

    Italy University of Milan (UMIL)
    Disease:

    Normal (average)

  2709. UNAMi001-A (IFC-UNAM iPD01-S)

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

    Parkinson disease

  2710. UNAMi002-A (IFC-UNAM iPD02-S)

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

    Parkinson disease

  2711. UNAMi003-A (IFC-UNAM iPD03-PINK1)

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

    Parkinson disease

  2712. UNEWi006-A

    United Kingdom University of Newcastle (UNEW)

  2713. UNEWi018-A

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Aplastic anemia

  2714. UNEWi019-A

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Anemia

  2715. UNEWi022-B (F181 18.2)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  2716. UNEWi022-C (F181 25.7)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  2717. UNEWi025-A (F324 5.8)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Age-related macular degeneration

  2718. UNEWe001-A (hES-NCL-1)

    United Kingdom University of Newcastle (UNEW)

  2719. UNEWe002-A (NCL-2)

    United Kingdom University of Newcastle (UNEW)

  2720. UNEWe004-A (NCL-4)

    United Kingdom University of Newcastle (UNEW)

  2721. UNEWe005-A (NCL-5)

    United Kingdom University of Newcastle (UNEW)

  2722. UNEWe006-A (NCL-6)

    United Kingdom University of Newcastle (UNEW)

  2723. UNEWe007-A (NCL-7)

    United Kingdom University of Newcastle (UNEW)

  2724. UNEWe008-A (NCL-8)

    United Kingdom University of Newcastle (UNEW)

  2725. UNEWe009-A (NCL-9)

    United Kingdom University of Newcastle (UNEW)

  2726. WAe009-A-O (CRX-GFP WAe009)

    United Kingdom University of Newcastle (UNEW)
    Disease:

    Normal (average)

  2727. UNIBSi017-A (EDS-iPSC)

    Italy University of Brescia (UNIBS)

  2728. UNIBSi018-A

    Italy University of Brescia (UNIBS)
    Disease:

    Noonan syndrome

  2729. UNIFEi001-A (iPSca1N1, MARPiPSCA1N1 and UniFei001-A)

    Italy University of Ferrara (UNIFE)
    Disease:

    Spinocerebellar ataxia type 1

  2730. UNIMGi011-A (PD-2M)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Parkinson disease

  2731. UNIMGi013-A (PRICKLE2 MUTsevere)

    Italy Università degli Studi Magna Graecia di Catanzaro (UNIMG)
    Disease:

    Epilepsy syndrome

  2732. UNIPDi004-A

    Italy University of Padova (UNIPD)
    Disease:

    Normal (average)

  2733. UNIPDi004-B (HDP04)

    Italy University of Padova (UNIPD)
    Disease:

    Normal (average)

  2734. UNIPDi006-A

    Italy University of Padova (UNIPD)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  2735. UNIPDi008-B (FXS GM05131 primed)

    Italy University of Padova (UNIPD)
    Disease:

    Fragile x syndrome

  2736. UNIPVi003-A (HDF109)

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

    Normal (average)

  2737. UNIZARi001-A (FiPSTK2-2)

    Spain University of Zaragoza (UNIZAR)
    Disease:

    Mitochondrial dna depletion syndrome, myopathic form

  2738. UOCi003-A-1 (A18 GPiPSC 31-1)

    Canada University of Calgary (UOC)
    Disease:

    Simplified gyral pattern

  2739. UOCi004-A

    Canada University of Calgary (UOC)
    Disease:

    Spondylocostal dysostosis

  2740. UOFTi004-A (BD001)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  2741. UOFTi005-A (BD002)

    Canada University of Toronto (UOFT)
    Disease:

    Bipolar disorder

  2742. UOFTi013-A (MS008)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  2743. UOFTi015-A (MS010)

    Canada University of Toronto (UOFT)
    Disease:

    Normal (average)

  2744. UOMi010-A (ANCS-hiPSC-HPP5)

    Canada University of Manitoba (UOM)
    Disease:

    Hypophosphatasia

  2745. UOMi013-A (GSACS-hiPSC-MELAS7)

    Canada University of Manitoba (UOM)
    Disease:

    Melas syndrome

  2746. UOSe003-A (Shef-3)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  2747. UOSe006-A (Shef-6)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  2748. UOSe007-A (MstrShef2, MShef2 and MasterShef2)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  2749. UOSe009-A (MstrShef4, MShef4 and MasterShef4)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  2750. UOSe010-A (MstrShef5, MShef5 and MasterShef5)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  2751. UOSe011-A (MstrShef6, MShef6 and MasterShef6)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  2752. UOSe013-A (MstrShef8, MasterShef8 and MShef8)

    United Kingdom University of Sheffield (UOS)
    Disease:

    Normal (average)

  2753. WAe009-A-W (H9 NGN2 B6)

    Australia University of Wollongong (UOW)
    Disease:

    Normal (average)

  2754. UOXFi001-C (MK071-5)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  2755. UOXFi001-D (MK071-6)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  2756. UOXFi002-A (MK082-26)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  2757. UOXFi002-B (MK082-30)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  2758. UOXFi003-A (MK088-1)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  2759. UOXFi006-A (OX2-28)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Normal (average)

  2760. UOXFi007-A (MK002-4)

    United Kingdom University of Oxford (UOXF)
    Disease:

    Parkinson disease

  2761. UPSFRi005-A (PB06)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Obsolete_down syndrome

  2762. UPSFRi005-A-1 (PB06-1)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Obsolete_down syndrome

  2763. UPSFRe002-A (CL02)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Monogenic disease

  2764. UPSFRe003-A (CL03)

    France Université Paris-Sud 11 (UPSFR)
    Disease:

    Chromosomal disease

  2765. UQi002-A (C3)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  2766. UQi003-A (C7)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  2767. UQi005-A (C13)

    Australia The University of Queensland (UQ)
    Disease:

    Normal (average)

  2768. UQACi001-A (iPSC-EBS21)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  2769. UQACi004-A (iPSC-EBS9)

    Canada Université du Québec à Chicoutimi (UQAC)
    Disease:

    Epidermolysis bullosa simplex

  2770. URi004-A

    Japan University of the Ryukyus (UR)
    Disease:

    Normal (average)

  2771. USCBi001-A (NIBSC_i008, NIBSC8,)

    United Kingdom National Institute for Biological Standards and Control - UK Stem Cell Bank (USCB)
    Disease:

    Normal (average)

  2772. USFi001-A (1CN1.5)

    United States University of South Florida (USF)
    Disease:

    Friedreich ataxia

  2773. USFi004-A (3IV6)

    United States University of South Florida (USF)
    Disease:

    Inherited arrhythmogenic cardiomyopathy

  2774. USPi001-A (iPS_LGH_AHDC1_P1)

    Brazil Universidade de São Paulo (USP)
    Disease:

    Xia-gibbs syndrome

  2775. UTSWi002-A (FA2)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Friedreich ataxia

  2776. WAe009-A-3L (H9-idCK-mC)

    United States University of Texas Southwestern Medical Center (UTSW)
    Disease:

    Normal (average)

  2777. UTUi001-B (TUR2)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  2778. UTUi001-C (TUR3)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  2779. UTUi002-A (TUR-STAB1-B1)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  2780. UTUi003-A (TUR-B1)

    Finland University of Turku (UTU)
    Disease:

    Normal (average)

  2781. VANYHHi001-A (AF13_VANYHH)

    United States VA New York Harbor Healthcare System (VANYHH)
    Disease:

    Brugada syndrome

  2782. VAPACLi001-A

    United States Veterans Affairs Palo Alto Health Care System: Chen Lab (VAPACL)
    Disease:

    Coronary artery vasospasm

  2783. VAPACLi002-A

    United States Veterans Affairs Palo Alto Health Care System: Chen Lab (VAPACL)
    Disease:

    Coronary artery vasospasm

  2784. VAPACLi003-A

    United States Veterans Affairs Palo Alto Health Care System: Chen Lab (VAPACL)
    Disease:

    Coronary artery vasospasm

  2785. VCCRIi003-A (SCAD-96 and 096)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Spontaneous coronary artery dissection

    Disease:

    Celiac disease

  2786. VCCRIi018-A (136 and SCAD-136)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Spontaneous coronary artery dissection

  2787. VCCRIi024-A (326)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Normal (average)

  2788. VCCRIi043-A (453)

    Australia Victor Chang Cardiac Research Institute (VCCRI)
    Disease:

    Niemann-pick disease, type c1

  2789. VHIRi003-A (RP25_UiPSC_mR5F_8)

    Spain Vall d'Hebron Institut de Recerca (VHIR)
    Disease:

    Normal (average)

  2790. VIACe001-A-2 (BG01V)

    United States Novocell, Inc. (VIAC)
    Disease:

    Klinefelter syndrome

  2791. VIACe003-A (hESBGN-03 (BG03))

    United States Novocell, Inc. (VIAC)

  2792. VRISGi002-A

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

    Normal (average)

  2793. VUi002-A (SCZ 18.10 and hvs483)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  2794. VUi004-A (SCZ 19.2 and hvs-484)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  2795. VUi008-A (SCZ 6.2)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  2796. VUi011-A (SCZ 3.5)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  2797. VUi013-A (804.3)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  2798. VUi021-A (793.3 and hvs473)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  2799. VUi023-A (801.A1 and hvs474)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  2800. VUi024-A (SCZ 9.4)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  2801. VUi029-A (hvs449a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  2802. VUi030-A (hvs450a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    4h leukodystrophy

  2803. VUi031-A (hvs88)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2804. VUi033-A (hvs445a and GM02036 Coriell)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2805. VUi036-A (hvs420 and GM23964)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2806. VUi038-A (hvs444a and GM01651 Coriell)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2807. VUi039-A (hvs446a and GM05381 Coriell)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2808. VUi042-A (GB2a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2809. VUi042-B (GB2f)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2810. VUi047-A (785.10 and hvs337)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Schizophrenia

  2811. VUi058-A (hvs521a and PEX1-024)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Zellweger spectrum disorders

  2812. VUi062-B (hvs512c and 7485267)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Ventricular fibrillation

  2813. VUi075-A (105.A, hvs498a and 685694)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2814. VUi075-C (105.C, hvs498c and 685694)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2815. VUi076-B (1005528, hvs499b and 509.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2816. VUi076-C (1005528, 509.C and hvs499c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2817. VUi077-B (hvs500b, 781085 and 315.B)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2818. VUi077-C (hvs500c, 315.C and 781085)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2819. VUi079-A (894067, 470.A and hvs502a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2820. VUi080-B (293.B, 770533 and hvs503b)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2821. VUi083-C (800835, 339.C and hvs506c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2822. VUi087-C (hvs510c, 305.C and 776639)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2823. VUi095-A (71066723 and hvs538c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Hao-fountain syndrome

  2824. VUi097-A (hvs557c)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Hao-fountain syndrome

  2825. VUi109-A (hvs517a and 2392816)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2826. VUi112-A (2086611 and hvs528a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Grin2b-related complex neurodevelopmental disorder

  2827. VUi113-A (2407481 and hvs529a)

    Netherlands Vrije Universiteit Amsterdam (VU)
    Disease:

    Normal (average)

  2828. VUBe009-A (VUB09_FSHD)

    Belgium Vrije Universiteit Brussel (VUB)
    Disease:

    Facioscapulohumeral muscular dystrophy

  2829. VUBe012-A (VUB12)

    Belgium Vrije Universiteit Brussel (VUB)

  2830. VUBe013-A (VUB13_FXS)

    Belgium Vrije Universiteit Brussel (VUB)
    Disease:

    Fragile x syndrome

  2831. CIGLi001-A-6 (VULSCi002-A-6)

    Lithuania Vilnius University (VULSC)
    Disease:

    Normal (average)

  2832. VUMCi001-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  2833. VUMCi002-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  2834. VUMCi003-A (1167)

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  2835. VUMCi004-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  2836. VUMCi005-A (3360)

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  2837. VUMCi006-A

    United States Vanderbilt University Medical Center (VUMC)
    Disease:

    Normal (average)

  2838. VUMCCVi001-A (NS15C5)

    United States Vanderbilt University Medical Center: Cardiovascular Medicine (VUMCCV)
    Disease:

    Normal (average)

  2839. VUMCCVi002-A (NS9C4)

    United States Vanderbilt University Medical Center: Cardiovascular Medicine (VUMCCV)
    Disease:

    Aortic valve stenosis

    Disease:

    Dyslipidemia

    Disease:

    Hypertension

  2840. VUMCCVi004-A (NS8C1)

    United States Vanderbilt University Medical Center: Cardiovascular Medicine (VUMCCV)
    Disease:

    Coronary artery disease

    Disease:

    Hyperlipidemia

    Disease:

    Atrial fibrillation

  2841. WAi001-B (DF19-9-7T and iPS-DF19-9-7T)

    United States WiCell Research Institute (WA)
    Disease:

    Normal (average)

  2842. WAe001-A (WA01 and H1)

    United States WiCell Research Institute (WA)
    Disease:

    Normal (average)

  2843. WAe013-A (WA13 and H13)

    United States WiCell Research Institute (WA)

  2844. WCHi005-A

    China West China Hospital (WCH)
    Disease:

    Bipolar disorder

  2845. WCHi006-A

    China West China Hospital (WCH)
    Disease:

    Schizophrenia

  2846. WIBRe002-A (WIBR2)

    United States Whitehead Institute for Biomedical Research (WIBR)
    Disease:

    Normal (average)

  2847. WISCi005-A (DS1 and UWWC1-DS1)

    United States University of Wisconsin (WISC)
    Disease:

    Trisomy 21

  2848. WISCi005-B (DS4 and UWWC1-DS4)

    United States University of Wisconsin (WISC)
    Disease:

    Trisomy 21

  2849. WISCi005-C (UWWC1-DS2U and DS2U)

    United States University of Wisconsin (WISC)
    Disease:

    Trisomy 21

  2850. WISCi006-A (2DS3 and UWWC1-2DS3)

    United States University of Wisconsin (WISC)
    Disease:

    Obsolete_down syndrome

  2851. WISCi007-A (WC026i-5807-3)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  2852. WISCi007-B (WC027i-5807-5)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  2853. WISCi008-A (WC029i-5907-1)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  2854. WISCi008-B (WC030i-5907-2)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  2855. WISCi009-A (WC032i-6007-1)

    United States University of Wisconsin (WISC)
    Disease:

    Normal (average)

  2856. WTSIi001-A (HPSI1213i-pahc_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2857. WTSIi002-A (HPSI0913i-eika_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2858. WTSIi012-A (HPSI0314i-bubh_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2859. WTSIi013-A (HPSI0214i-kucg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2860. WTSIi017-A (HPSI0114i-lexy_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2861. WTSIi019-B (HPSI0114i-iisa_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2862. WTSIi045-A (HPSI0214i-heth_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2863. WTSIi047-A (HPSI0814i-bokz_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2864. WTSIi047-B (HPSI0814i-bokz_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2865. WTSIi049-A (HPSI0514i-wiii_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2866. WTSIi049-B (HPSI0514i-wiii_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2867. WTSIi052-A (HPSI1114i-ziyn_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2868. WTSIi053-A (HPSI0413i-corn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2869. WTSIi055-A (HPSI0513i-debk_9)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2870. WTSIi056-A (HPSI0513i-dipe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2871. WTSIi059-A (HPSI0513i-uilw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2872. WTSIi063-A (HPSI0613i-aevs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2873. WTSIi069-A (HPSI0613i-hegp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2874. WTSIi072-A (HPSI0114i-fikt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2875. WTSIi073-A (HPSI0314i-sojd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2876. WTSIi077-A (HPSI0314i-cuhk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2877. WTSIi081-A (HPSI1113i-qorq_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2878. WTSIi082-A (HPSI1013i-cups_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2879. WTSIi085-A (HPSI1113i-eofe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2880. WTSIi086-A (HPSI0913i-coyi_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2881. WTSIi089-A (HPSI0613i-xavk_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2882. WTSIi098-A (HPSI1213i-nekd_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2883. WTSIi102-A (HPSI0413i-iakz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2884. WTSIi102-B (HPSI0413i-iakz_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2885. WTSIi103-A (HPSI1213i-nusw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2886. WTSIi104-A (HPSI0513i-coio_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2887. WTSIi104-B (HPSI0513i-coio_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2888. WTSIi106-B (HPSI0613i-hikj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2889. WTSIi109-A (HPSI0413i-coxy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2890. WTSIi109-B (HPSI0413i-coxy_33)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2891. WTSIi110-A (HPSI0713i-darw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2892. WTSIi111-A (HPSI0513i-euir_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2893. WTSIi114-A (HPSI0513i-golb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2894. WTSIi115-A (HPSI0513i-iasn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2895. WTSIi116-A (HPSI0813i-iicq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2896. WTSIi117-A (HPSI0613i-liun_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2897. WTSIi117-B (HPSI0613i-liun_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2898. WTSIi118-A (HPSI0813i-meqo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2899. WTSIi119-A (HPSI0613i-oefg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2900. WTSIi120-A (HPSI0513i-oeoo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2901. WTSIi121-A (HPSI0413i-ougl_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2902. WTSIi128-A (HPSI0413i-yuze_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2903. WTSIi135-A (HPSI0214i-feec_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2904. WTSIi136-A (HPSI0913i-iuqb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2905. WTSIi141-A (HPSI0613i-qanu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2906. WTSIi143-A (HPSI0214i-rayr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2907. WTSIi146-A (HPSI0613i-xosg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2908. WTSIi153-A (HPSI0414i-puvg_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  2909. WTSIi159-A (HPSI0714i-gibe_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  2910. WTSIi160-A (HPSI0914i-verf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  2911. WTSIi161-A (HPSI0714i-rajk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  2912. WTSIi162-A (HPSI0914i-lopq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  2913. WTSIi163-A (HPSI1014i-suok_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  2914. WTSIi172-A (HPSI0914i-laey_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2915. WTSIi173-A (HPSI0414i-naju_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2916. WTSIi174-A (HPSI0614i-paab_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2917. WTSIi175-A (HPSI1014i-tixi_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2918. WTSIi198-A (HPSI0414i-fuai_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  2919. WTSIi201-A (HPSI0614i-koqx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  2920. WTSIi202-A (HPSI0714i-oebj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  2921. WTSIi204-A (HPSI0414i-oulr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  2922. WTSIi209-A (HPSI0613i-dium_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2923. WTSIi211-A (HPSI0513i-huls_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2924. WTSIi212-A (HPSI0613i-auim_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2925. WTSIi213-A (HPSI0713i-kaks_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2926. WTSIi214-A (HPSI0513i-leeh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2927. WTSIi216-A (HPSI0613i-riiv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2928. WTSIi217-A (HPSI0513i-cuau_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2929. WTSIi218-A (HPSI0914i-euts_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2930. WTSIi219-A (HPSI0613i-jorr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2931. WTSIi222-A (HPSI0613i-vorx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2932. WTSIi223-A (HPSI0813i-piun_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2933. WTSIi225-A (HPSI0513i-xegx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2934. WTSIi227-A (HPSI1113i-wetu_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2935. WTSIi228-A (HPSI0514i-qihv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2936. WTSIi232-A (HPSI0613i-focm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2937. WTSIi233-A (HPSI0513i-cehw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2938. WTSIi235-A (HPSI0513i-uoxz_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2939. WTSIi236-A (HPSI0813i-voas_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2940. WTSIi238-A (HPSI0914i-suop_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2941. WTSIi241-A (HPSI0913i-lofv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2942. WTSIi243-A (HPSI0414i-ceik_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2943. WTSIi245-A (HPSI0714i-keui_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2944. WTSIi247-A (HPSI0614i-oicx_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2945. WTSIi248-A (HPSI0213i-koun_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2946. WTSIi249-A (HPSI0614i-uilk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2947. WTSIi250-A (HPSI0115i-melw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2948. WTSIi250-B (HPSI0115i-melw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2949. WTSIi252-A (HPSI0115i-vazt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2950. WTSIi252-B (HPSI0115i-vazt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2951. WTSIi253-A (HPSI0514i-letw_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2952. WTSIi254-A (HPSI0914i-jejf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2953. WTSIi255-A (HPSI0115i-aion_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2954. WTSIi255-B (HPSI0115i-aion_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2955. WTSIi256-A (HPSI1014i-tuju_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2956. WTSIi256-B (HPSI1014i-tuju_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2957. WTSIi257-A (HPSI0714i-burb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2958. WTSIi258-A (HPSI0913i-bulb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2959. WTSIi259-A (HPSI0514i-vuna_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2960. WTSIi260-A (HPSI0414i-oikd_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2961. WTSIi261-A (HPSI1113i-wahn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2962. WTSIi262-A (HPSI0514i-sohd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2963. WTSIi263-A (HPSI0614i-lepk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2964. WTSIi265-A (HPSI0714i-pipw_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2965. WTSIi266-A (HPSI0115i-gifk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2966. WTSIi267-A (HPSI0115i-iiyk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2967. WTSIi267-B (HPSI0115i-iiyk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2968. WTSIi268-A (HPSI0714i-nufh_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2969. WTSIi269-A (HPSI0115i-hecn_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2970. WTSIi269-B (HPSI0115i-hecn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2971. WTSIi270-A (HPSI0514i-fiaj_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2972. WTSIi271-A (HPSI0414i-gesg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2973. WTSIi274-A (HPSI0714i-jilk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2974. WTSIi275-A (HPSI0115i-uolo_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2975. WTSIi276-A (HPSI1014i-juuy_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2976. WTSIi277-A (HPSI1114i-ualf_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2977. WTSIi279-A (HPSI0813i-ffdj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2978. WTSIi281-A (HPSI0115i-qoog_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2979. WTSIi283-A (HPSI0514i-toco_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2980. WTSIi284-A (HPSI0614i-liqa_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2981. WTSIi285-A (HPSI0414i-sebn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2982. WTSIi287-A (HPSI0514i-lako_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2983. WTSIi288-A (HPSI0715i-meue_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2984. WTSIi291-A (HPSI0215i-yoch_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2985. WTSIi293-A (HPSI0215i-deyz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2986. WTSIi294-A (HPSI1014i-bilx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2987. WTSIi294-B (HPSI1014i-bilx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2988. WTSIi296-A (HPSI0214i-giju_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2989. WTSIi297-A (HPSI0813i-fpdl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2990. WTSIi299-A (HPSI0213i-nawk_55)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2991. WTSIi300-A (HPSI0714i-kute_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2992. WTSIi302-A (HPSI1014i-nosn_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2993. WTSIi302-B (HPSI1014i-nosn_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2994. WTSIi303-A (HPSI0914i-qehq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2995. WTSIi308-A (HPSI0115i-zihe_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2996. WTSIi310-A (HPSI0614i-ciwj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2997. WTSIi311-A (HPSI0215i-hipn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2998. WTSIi316-A (HPSI0514i-kuco_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  2999. WTSIi317-A (HPSI1014i-eesb_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3000. WTSIi318-A (HPSI1014i-sehl_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3001. WTSIi322-A (HPSI0514i-naah_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3002. WTSIi327-A (HPSI0715i-zaie_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3003. WTSIi341-A (HPSI1014i-riun_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3004. WTSIi342-A (HPSI0613i-ueah_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3005. WTSIi345-A (HPSI0715i-aowh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3006. WTSIi347-A (HPSI0814i-doao_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3007. WTSIi349-A (HPSI0914i-gine_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3008. WTSIi350-A (HPSI0513i-momt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3009. WTSIi351-A (HPSI0513i-oibg_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3010. WTSIi353-A (HPSI0914i-ouvb_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3011. WTSIi354-A (HPSI0513i-netf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3012. WTSIi355-A (HPSI0413i-yotv_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3013. WTSIi362-A (HPSI0513i-oarz_22)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3014. WTSIi363-A (HPSI1014i-vils_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3015. WTSIi364-A (HPSI1013i-zagm_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3016. WTSIi368-A (HPSI0914i-iezw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3017. WTSIi369-A (HPSI0514i-uenn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3018. WTSIi370-A (HPSI0613i-nukw_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3019. WTSIi373-A (HPSI1013i-jogf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3020. WTSIi374-A (HPSI1014i-roug_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3021. WTSIi377-A (HPSI0713i-veku_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3022. WTSIi378-A (HPSI0713i-nocf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3023. WTSIi380-A (HPSI0713i-pusf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3024. WTSIi382-A (HPSI0614i-denw_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3025. WTSIi385-A (HPSI0713i-fett_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3026. WTSIi387-A (HPSI0513i-dovq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3027. WTSIi388-A (HPSI0115i-paim_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3028. WTSIi389-A (HPSI0614i-voce_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3029. WTSIi390-A (HPSI1113i-hajc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3030. WTSIi392-A (HPSI0513i-sucd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3031. WTSIi394-A (HPSI0914i-vaka_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3032. WTSIi396-A (HPSI0414i-kodf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3033. WTSIi398-A (HPSI0414i-rauj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3034. WTSIi399-A (HPSI0614i-gawh_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3035. WTSIi400-A (HPSI0414i-tout_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3036. WTSIi402-A (HPSI0714i-ouzk_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3037. WTSIi403-A (HPSI0913i-rufg_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3038. WTSIi406-A (HPSI0614i-mesr_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3039. WTSIi407-A (HPSI0914i-hidy_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3040. WTSIi408-A (HPSI0414i-niim_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3041. WTSIi409-A (HPSI0414i-walu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3042. WTSIi410-A (HPSI0614i-zoio_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3043. WTSIi411-A (HPSI0914i-rejf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3044. WTSIi412-A (HPSI0614i-wihj_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3045. WTSIi416-A (HPSI0514i-aomr_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3046. WTSIi417-A (HPSI0614i-voxu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3047. WTSIi419-A (HPSI0514i-kidt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3048. WTSIi420-A (HPSI0914i-tifo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3049. WTSIi420-B (HPSI0914i-tifo_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3050. WTSIi422-A (HPSI0414i-zazi_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3051. WTSIi424-A (HPSI0514i-mure_9)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3052. WTSIi426-A (HPSI0714i-mejk_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3053. WTSIi428-A (HPSI0714i-lutt_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3054. WTSIi430-A (HPSI0514i-aecv_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3055. WTSIi430-B (HPSI0514i-aecv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3056. WTSIi431-A (HPSI0514i-tavh_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3057. WTSIi436-A (HPSI0714i-zaos_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3058. WTSIi438-A (HPSI0714i-pirs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3059. WTSIi447-A (HPSI0416i-zige_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3060. WTSIi447-B (HPSI0416i-zige_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3061. WTSIi448-A (HPSI0316i-muwv_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3062. WTSIi448-B (HPSI0316i-muwv_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3063. WTSIi450-A (HPSI0216i-aiid_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3064. WTSIi450-B (HPSI0216i-aiid_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3065. WTSIi453-A (HPSI0416i-fiwt_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3066. WTSIi454-A (HPSI0516i-iool_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3067. WTSIi454-B (HPSI0516i-iool_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3068. WTSIi455-A (HPSI0516i-eosr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  3069. WTSIi456-A (HPSI0616i-kulz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  3070. WTSIi457-A (HPSI0115i-iinu_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3071. WTSIi457-B (HPSI0115i-iinu_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3072. WTSIi458-A (HPSI0614i-lipl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3073. WTSIi458-B (HPSI0614i-lipl_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3074. WTSIi459-A (HPSI0516i-zukb_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3075. WTSIi459-B (HPSI0516i-zukb_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3076. WTSIi460-A (HPSI0516i-jepf_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3077. WTSIi460-B (HPSI0516i-jepf_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3078. WTSIi461-A (HPSI0316i-eoko_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3079. WTSIi461-B (HPSI0316i-eoko_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3080. WTSIi462-A (HPSI0316i-miov_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3081. WTSIi463-A (HPSI0716i-yibs_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  3082. WTSIi464-A (HPSI0516i-eitu_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3083. WTSIi464-B (HPSI0516i-eitu_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3084. WTSIi465-A (HPSI0714i-xiry_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3085. WTSIi466-A (HPSI0416i-aicq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3086. WTSIi466-B (HPSI0416i-aicq_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3087. WTSIi467-A (HPSI0513i-bicb_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3088. WTSIi468-A (HPSI1013i-woci_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3089. WTSIi470-A (HPSI0516i-jory_9)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3090. WTSIi470-B (HPSI0516i-jory_10)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3091. WTSIi472-A (HPSI0216i-vieg_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3092. WTSIi472-B (HPSI0216i-vieg_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3093. WTSIi473-A (HPSI0813i-mioj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3094. WTSIi474-A (HPSI0216i-dewh_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3095. WTSIi474-B (HPSI0216i-dewh_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3096. WTSIi475-A (HPSI0514i-qajt_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3097. WTSIi476-A (HPSI0813i-peoj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3098. WTSIi477-A (HPSI0514i-kooz_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3099. WTSIi478-A (HPSI0414i-nolz_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3100. WTSIi479-A (HPSI0616i-beyk_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  3101. WTSIi480-A (HPSI0516i-iuoc_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3102. WTSIi480-B (HPSI0516i-iuoc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3103. WTSIi481-A (HPSI0716i-toba_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  3104. WTSIi482-A (HPSI0616i-gayk_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  3105. WTSIi483-A (HPSI0416i-ourj_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3106. WTSIi483-B (HPSI0416i-ourj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3107. WTSIi484-A (HPSI0716i-bakv_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3108. WTSIi484-B (HPSI0716i-bakv_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3109. WTSIi485-A (HPSI0614i-kecw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3110. WTSIi486-A (HPSI0516i-hapz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3111. WTSIi486-B (HPSI0516i-hapz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3112. WTSIi487-A (HPSI0516i-goek_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3113. WTSIi488-A (HPSI0516i-oazw_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3114. WTSIi488-B (HPSI0516i-oazw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3115. WTSIi493-A (HPSI0416i-ruah_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3116. WTSIi493-B (HPSI0416i-ruah_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3117. WTSIi495-A (HPSI0314i-kujn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3118. WTSIi496-A (HPSI0516i-yibc_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3119. WTSIi497-A (HPSI0616i-oajt_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  3120. WTSIi498-A (HPSI0616i-biln_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  3121. WTSIi499-A (HPSI0416i-xutl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3122. WTSIi501-A (HPSI0316i-circ_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  3123. WTSIi502-A (HPSI0216i-boho_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3124. WTSIi503-A (HPSI0416i-mapx_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  3125. WTSIi506-A (HPSI0616i-giql_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  3126. WTSIi507-A (HPSI0614i-uevq_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3127. WTSIi508-A (HPSI0416i-jewl_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3128. WTSIi508-B (HPSI0416i-jewl_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3129. WTSIi509-A (HPSI0416i-ourj_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3130. WTSIi510-A (HPSI0216i-xanu_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3131. WTSIi510-B (HPSI0216i-xanu_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3132. WTSIi512-A (HPSI0416i-ruah_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3133. WTSIi514-A (HPSI0416i-iooi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3134. WTSIi514-B (HPSI0416i-iooi_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3135. WTSIi515-A (HPSI0416i-bife_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  3136. WTSIi516-A (HPSI0216i-iogu_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3137. WTSIi516-B (HPSI0216i-iogu_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3138. WTSIi518-A (HPSI0416i-cihd_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  3139. WTSIi519-A (HPSI0416i-sevr_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  3140. WTSIi522-A (HPSI0516i-pews_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3141. WTSIi522-B (HPSI0516i-pews_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3142. WTSIi524-A (HPSI0616i-xuvy_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  3143. WTSIi525-A (HPSI0616i-bury_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  3144. WTSIi526-A (HPSI0316i-qeti_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  3145. WTSIi527-A (HPSI0216i-heub_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3146. WTSIi527-B (HPSI0216i-heub_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3147. WTSIi529-A (HPSI0716i-yipp_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  3148. WTSIi530-A (HPSI0215i-zett_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3149. WTSIi531-A (HPSI0616i-kayf_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  3150. WTSIi534-A (HPSI0616i-eomr_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  3151. WTSIi545-A (HPSI0416i-eapo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  3152. WTSIi548-A (HPSI0416i-mefc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3153. WTSIi548-B (HPSI0416i-mefc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3154. WTSIi554-A (HPSI0216i-dacv_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3155. WTSIi555-A (HPSI0316i-xaqm_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Congenital hyperinsulinism

  3156. WTSIi558-A (HPSI0516i-oadp_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  3157. WTSIi560-A (HPSI0214i-bute_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3158. WTSIi561-A (HPSI0813i-aomg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3159. WTSIi563-A (HPSI0516i-zujs_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3160. WTSIi564-A (HPSI0313i-fecs_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3161. WTSIi565-A (HPSI0313i-xovo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3162. WTSIi567-A (HPSI0813i-eiqh_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3163. WTSIi568-A (HPSI0216i-rihx_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3164. WTSIi569-A (HPSI0613i-qonr_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3165. WTSIi570-A (HPSI0213i-koun_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3166. WTSIi571-A (HPSI0513i-pedc_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3167. WTSIi573-A (HPSI0115i-qaqp_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3168. WTSIi573-B (HPSI0115i-qaqp_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Bardet-biedl syndrome

  3169. WTSIi576-A (HPSI0216i-feht_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3170. WTSIi580-A (HPSI0316i-aask_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Kabuki syndrome

  3171. WTSIi582-A (HPSI0613i-oesx_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3172. WTSIi590-A (HPSI0115i-gost_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3173. WTSIi591-A (HPSI0514i-oupf_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3174. WTSIi593-A (HPSI0514i-tert_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3175. WTSIi594-A (HPSI0115i-aoxv_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3176. WTSIi595-A (HPSI0814i-siqu_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3177. WTSIi596-A (HPSI0514i-oekw_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3178. WTSIi597-A (HPSI0414i-uawq_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3179. WTSIi598-A (HPSI1114i-kuul_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3180. WTSIi598-B (HPSI1114i-kuul_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3181. WTSIi599-A (HPSI0614i-lirf_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3182. WTSIi599-B (HPSI0614i-lirf_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3183. WTSIi602-A (HPSI0614i-puhk_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3184. WTSIi603-A (HPSI0614i-qunz_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3185. WTSIi607-A (HPSI1014i-xiyh_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3186. WTSIi609-A (HPSI0516i-suqd_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3187. WTSIi609-B (HPSI0516i-suqd_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3188. WTSIi610-A (HPSI1116i-naum_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  3189. WTSIi611-A (HPSI0816i-neow_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  3190. WTSIi612-A (HPSI0616i-mifg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  3191. WTSIi613-A (HPSI1116i-rafd_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  3192. WTSIi615-A (HPSI0115i-rakq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3193. WTSIi615-B (HPSI0115i-rakq_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3194. WTSIi617-A (HPSI0215i-uiao_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3195. WTSIi618-A (HPSI1114i-xiby_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3196. WTSIi618-B (HPSI1114i-xiby_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3197. WTSIi619-A (HPSI0115i-kozf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3198. WTSIi619-B (HPSI0115i-kozf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3199. WTSIi620-A (HPSI0616i-uegn_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  3200. WTSIi621-A (HPSI0916i-vorn_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3201. WTSIi621-B (HPSI0916i-vorn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3202. WTSIi622-A (HPSI0516i-menz_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3203. WTSIi622-B (HPSI0516i-menz_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3204. WTSIi623-A (HPSI0516i-yist_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  3205. WTSIi624-A (HPSI0616i-uofs_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  3206. WTSIi626-A (HPSI0914i-yuvg_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3207. WTSIi633-A (HPSI0714i-oatm_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3208. WTSIi634-A (HPSI0115i-timk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3209. WTSIi635-A (HPSI0414i-zabk_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_monogenic diabetes

  3210. WTSIi636-A (HPSI0514i-yewo_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3211. WTSIi638-A (HPSI0916i-zipi_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3212. WTSIi638-B (HPSI0916i-zipi_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3213. WTSIi641-A (HPSI0516i-aaun_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3214. WTSIi641-B (HPSI0516i-aaun_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3215. WTSIi643-A (HPSI0514i-suul_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3216. WTSIi643-B (HPSI0514i-suul_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3217. WTSIi644-A (HPSI0115i-sehp_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3218. WTSIi644-B (HPSI0115i-sehp_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3219. WTSIi645-A (HPSI0514i-xufp_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3220. WTSIi646-A (HPSI1114i-zuuy_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3221. WTSIi646-B (HPSI1114i-zuuy_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3222. WTSIi648-A (HPSI0616i-mesv_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  3223. WTSIi654-A (HPSI0115i-uupc_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3224. WTSIi657-A (HPSI0916i-moyn_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  3225. WTSIi658-A (HPSI0816i-fuuy_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  3226. WTSIi659-A (HPSI1116i-wakr_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  3227. WTSIi660-A (HPSI0115i-tiku_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3228. WTSIi660-B (HPSI0115i-tiku_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3229. WTSIi661-A (HPSI0614i-xubw_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3230. WTSIi662-A (HPSI1116i-mebq_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3231. WTSIi662-B (HPSI1116i-mebq_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3232. WTSIi665-A (HPSI0616i-euia_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  3233. WTSIi666-A (HPSI0514i-xayd_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3234. WTSIi669-A (HPSI0816i-aorf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3235. WTSIi669-B (HPSI0816i-aorf_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Usher syndrome

  3236. WTSIi670-A (HPSI0614i-juzt_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3237. WTSIi672-A (HPSI0516i-quqp_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3238. WTSIi672-B (HPSI0516i-quqp_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3239. WTSIi673-A (HPSI0616i-vaqx_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  3240. WTSIi674-A (HPSI1116i-vozo_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  3241. WTSIi674-B (HPSI1116i-vozo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Alport syndrome

  3242. WTSIi675-A (HPSI0616i-iuse_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  3243. WTSIi676-A (HPSI0616i-heba_11)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  3244. WTSIi679-A (HPSI0316i-ponl_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3245. WTSIi679-B (HPSI0316i-ponl_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3246. WTSIi680-A (HPSI0516i-peoo_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  3247. WTSIi685-A (HPSI0416i-ioys_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3248. WTSIi685-B (HPSI0416i-ioys_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3249. WTSIi686-A (HPSI0616i-baxr_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  3250. WTSIi687-A (HPSI0916i-vajy_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete: genetic macular dystrophy

  3251. WTSIi688-A (HPSI1116i-wiau_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  3252. WTSIi689-A (HPSI0616i-newl_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare hypertrophic cardiomyopathy

  3253. WTSIi690-A (HPSI0115i-jotn_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3254. WTSIi690-B (HPSI0115i-jotn_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3255. WTSIi691-A (HPSI1116i-eiyy_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  3256. WTSIi693-A (HPSI1116i-zies_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  3257. WTSIi694-A (HPSI0816i-oemk_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  3258. WTSIi697-A (HPSI0516i-dewa_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3259. WTSIi697-B (HPSI0516i-dewa_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3260. WTSIi698-A (HPSI1116i-aimh_5)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  3261. WTSIi699-A (HPSI0916i-hikt_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3262. WTSIi699-B (HPSI0916i-hikt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3263. WTSIi700-A (HPSI0115i-iuad_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3264. WTSIi700-B (HPSI0115i-iuad_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3265. WTSIi703-A (HPSI0816i-hizl_3)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Spastic paraplegia

  3266. WTSIi705-A (HPSI0314i-xagu_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3267. WTSIi709-A (HPSI0516i-kumr_11)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete cln3 disease

  3268. WTSIi712-A (HPSI1016i-riwg_8)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Rare genetic neurological disorder

  3269. WTSIi713-A (HPSI0816i-xoga_7)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Retinitis pigmentosa

  3270. WTSIi715-A (HPSI0115i-payf_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3271. WTSIi717-A (HPSI0916i-helh_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3272. WTSIi717-B (HPSI0916i-helh_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3273. WTSIi718-A (HPSI0616i-duve_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Obsolete_immune system disease

  3274. WTSIi720-A (HPSI0916i-jejm_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hereditary ataxia

  3275. WTSIi722-A (HPSI0115i-jakt_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3276. WTSIi726-A (HPSI0115i-boqx_2)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3277. WTSIi727-A (HPSI0115i-bimq_4)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3278. WTSIi732-A (HPSI0616i-kalo_6)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Hematologic disease

  3279. WTSIi740-A (HPSI0215i-romx_1)

    United Kingdom Wellcome Sanger Institute (WTSI)
    Disease:

    Normal (average)

  3280. WYUi004-A (WYU-G6)

    China Wuyi University (WYU)
    Disease:

    Normal (average)

  3281. XMUi001-A

    China Xiamen University (XMU)
    Disease:

    Primary coenzyme q10 deficiency 7

  3282. XWHNi003-A

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

    Alzheimer's disease

  3283. XWHNi004-A

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

    Normal (average)

  3284. YBLi001-A (YBL/IPSC01/CONTROL)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  3285. YBLi002-A (YBL/IPSC002/CONTROL)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  3286. YBLi004-A (YBL/SH/2018/0062)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  3287. YBLi005-A (YBL/OS/2021/00196)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  3288. YBLi007-A (YBL/SH/2018/0067)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  3289. YBLi008-A (YBL/SH/2018/0050)

    India Yashraj Biotechnology ltd Navi Mumbai India (YBL)
    Disease:

    Normal (average)

  3290. YCMi004-A

    South Korea College of Medicine (YCM)
    Disease:

    Dilated cardiomyopathy

  3291. YCMi009-A (YCMi009-hDCM009-A)

    South Korea College of Medicine (YCM)
    Disease:

    Obsolete_dilated cardiomyopathy

  3292. YSCHi002-A (2ABWS)

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

    Obsolete_epilepsy

  3293. YUi002-A (VK0846 #1 and ASmut1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  3294. YUi004-A (PZ8594 #2 and ASmut3)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  3295. YUi007-A (SD6010 #3 and ASdel2)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  3296. YUi009-A (DY5863 #21 and ASupd1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  3297. YUi010-A (AK7856 #1 and ASupd2)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  3298. YUi011-A (ZM9576 #9 and ASupd3)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  3299. YUi012-A (QC7748 #2 and ASupd4)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  3300. YUi013-A (UI5640 #8 and ASicd1)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  3301. YUi014-A (DX6976 #7 and ASicd2)

    United States Yale University (YU)
    Disease:

    Angelman syndrome

  3302. YUi016-A (VJ9612 #5 and ASctr1)

    United States Yale University (YU)
    Disease:

    Normal (average)

  3303. ZIPi013-B (ZIP13 clone 2)

    Germany Zentrum für Integrative Psychiatrie-ZiP gGmbH, Stem Cell Lab (ZIP)
    Disease:

    Normal (average)

  3304. ZJUCi001-A

    China Zhejiang children hospital (ZJUC)
    Disease:

    Dilated cardiomyopathy

  3305. ZZUi004-A (ZZU-iPS-SCA3-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 3

  3306. ZZUi013-A (ZZU-iPS-AD-MEOX2-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Obsolete_alzheimer's disease

  3307. ZZUi017-A (ZZU-iPS-SCA6-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Spinocerebellar ataxia type 6

  3308. ZZUi019-A (ZZU-iPS-Normal-002)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  3309. ZZUi036-A (ZZU-iPS-NIID-NOTCH2NLC-001)

    China The first affiliated hospital (ZZU)
    Disease:

    Normal (average)

  3310. ZZUCSBi001-A

    China Shu-Ang Li (ZZUCSB)
    Disease:

    Normal (average)

  3311. ZZUNEUi010-A (CMF001-A)

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

    Juvenile amyotrophic lateral sclerosis

  3312. ZZUNEUi027-A

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

    Long qt syndrome 2

  3313. WAe009-A-Z

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

    Obsolete_congenital heart disease

  3314. WAe009-A-C

    China The Second Affiliated Hospital (ZZUSA)
    Disease:

    Heart failure

  3315. ZZUSAHi004-A

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

    Familial long qt syndrome

  3316. WAe009-A-P

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

    Cardiac valvular defect