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Summary Literature (0)
DOID:0110849 - xeroderma pigmentosum group G


Disease Ontology Definition:A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33.

Synonyms: XP group G, XP7, XPG, xeroderma pigmentosum VII

Xenbase Genes : ercc5

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010216 - xeroderma pigmentosum group G

OMIM:
OMIM:278780 - XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG

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)