ID   GM16549
AC   CVCL_X436
DR   Coriell; GM16549
DR   Wikidata; Q54848637
CC   Derived from site: In situ; Placenta; UBERON=UBERON_0001987.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C85071; Smith-Lemli-Opitz syndrome
DI   ORDO; Orphanet_818; Smith-Lemli-Opitz syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   1D
CA   Finite cell line
DT   Created: 05-09-14; Last updated: 29-06-23; Version: 7
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