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Summary Literature (0)
DOID:0110848 - xeroderma pigmentosum group F

Disease Ontology Definition:A xeroderma pigmentosum characterized by milder symptoms and later onset of skin cancer that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC4 gene on chromosome 16p13.

Synonyms: XP group F, XP6, XPF, xeroderma pigmentosum VI,

Xenbase Genes : ercc4

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010215 - xeroderma pigmentosum group F


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): xeroderma pigmentosum (is_a)