ID   DD2644
AC   CVCL_9K50
DR   ECACC; 96050810
DR   Wikidata; Q54830324
CC   Part of: ECACC chromosomal abnormality collection.
CC   Karyotypic information: 46,XY.ish 22q11-2(cH748x2) (ECACC=96050810).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
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: 23-02-16; Last updated: 29-06-23; Version: 6
//