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

Echinobase Genes : ercc4


MIM:
MIM:278760 - xeroderma pigmentosum, complementation group f; xpf

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

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