ID   HPSI0916i-moyn_1
AC   CVCL_LM47
SY   WTSIi657-B; WTSIi711-A
DR   BioSamples; SAMEA104130575
DR   ECACC; 77650761
DR   HipSci; HPSI0916i-moyn_1
DR   hPSCreg; WTSIi657-B
DR   Wikidata; Q54891529
CC   From: University College London; London; United Kingdom.
CC   From: Wellcome Trust Sanger Institute; Hinxton; United Kingdom.
CC   Population: Caucasian.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C140264; Genetic macular dystrophy
DI   ORDO; Orphanet_522574; Rare genetic macular disorder
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_LM48 ! HPSI0916i-moyn_4
SX   Male
AG   55-59Y
CA   Induced pluripotent stem cell
DT   Created: 15-11-17; Last updated: 29-06-23; Version: 11
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