ID   GM16627
AC   CVCL_DS91
DR   CLO; CLO_0017349
DR   Coriell; GM16627
DR   Wikidata; Q54848673
CC   Derived from site: In situ; Chest, skin; UBERON=UBERON_0001868.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C35337; Congenital nephrotic syndrome
DI   ORDO; Orphanet_564127; Genetic nephrotic syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   3M
CA   Finite cell line
DT   Created: 13-07-16; Last updated: 29-06-23; Version: 8
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