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DOID:0110844 - xeroderma pigmentosum group C
Disease Ontology Definition:A xeroderma pigmentosum characterized by increased propensity to develop malignant melanoma that has_material_basis_in mutation in the XPC gene on chromosome 3p25.
Synonyms: XP group C, XP3, XPC, XPCC, xeroderma pigmentosum III
Echinobase Genes

MIM:278720 - xeroderma pigmentosum, complementation group c; xpc |
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)