ID   PBD1-Fib
AC   CVCL_WC38
SY   Peroxisome Biogenesis Disorder 1-Fibroblast
DR   IBRC; C10511
DR   Wikidata; Q98128489
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C85239; Zellweger syndrome
DI   ORDO; Orphanet_912; Zellweger syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   2M
CA   Finite cell line
DT   Created: 24-05-19; Last updated: 29-06-23; Version: 7
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