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Summary Literature (0)
MIM:278780 - XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG

Xenbase Genes: ercc5

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008926 - COFS syndrome
MONDO:0010216 - xeroderma pigmentosum group G
MONDO:0016006 - Cockayne syndrome
MONDO:0016354 - xeroderma pigmentosum-Cockayne syndrome complex
MONDO:0019600 - xeroderma pigmentosum

Disease Ontology (DO):
DOID:0110849 - xeroderma pigmentosum group G