ID   PBD2-Fib
AC   CVCL_WC39
SY   Peroxisome Biogenesis Disorder 2-Fibroblast
DR   IBRC; C10508
DR   Wikidata; Q98128490
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C85047; Rhizomelic chondrodysplasia punctata
DI   ORDO; Orphanet_177; Rhizomelic chondrodysplasia punctata
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   6Y
CA   Finite cell line
DT   Created: 24-05-19; Last updated: 29-06-23; Version: 7
//