ID   GM20613
AC   CVCL_DS98
DR   CLO; CLO_0028956
DR   Coriell; GM20613
DR   Wikidata; Q54851134
CC   Derived from site: In situ; Fetal umbilical vein; UBERON=UBERON_0002066.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C122795; Nephrotic syndrome - NPHS1 associated
DI   ORDO; Orphanet_839; Congenital nephrotic syndrome, Finnish type
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   18FW
CA   Finite cell line
DT   Created: 13-07-16; Last updated: 29-06-23; Version: 9
//