Term Name:	xeroderma pigmentosum group G
Synonyms:	xeroderma pigmentosum VII, XP group G, XP7, XPG
Definition:	A xeroderma pigmentosum that has_material_basis_in homozygous or compound heterozygous mutation in the ERCC5 gene on chromosome 13q33.
Ontology:	Human Disease [DOID:0110849]   ( DOID:0110849 )