ID   HFSK9t
AC   CVCL_B504
DR   RCB; RCB1542
DR   Wikidata; Q54883303
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C84282; Trisomy 9
DI   ORDO; Orphanet_98131; Total autosomal trisomy
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_B503 ! HFL9t
SX   Male
AG   19FW
CA   Finite cell line
DT   Created: 06-06-12; Last updated: 29-06-23; Version: 9
//