has material basis in germline mutation in XPC xeroderma pigmentosum group C https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/xeroderma_pigmentosum_complementation_group_c https://www.malacards.org/card/xeroderma_pigmentosum_group_c_2 XP-C UMLS:C2752147 xeroderma pigmentosum, group C SCTID:25784009 MONDO:0010211 MEDGEN:416702 xeroderma pigmentosum 3 xeroderma pigmentosum, complementation group C xeroderma pigmentosum group C Orphanet:276255 xeroderma pigmentosum, type 3 GARD:0005626 MESH:C567886 DOID:0110844 XP3 An autosomal recessive inherited disorder caused by mutations in the XPC gene. This disease is characterized by increased sensitivity to sunlight with the development of carcinomas at an early age and is caused by a defect in nucleotide excision repair. XPCC NCIT:C114770 xeroderma pigmentosum, complementation group type C xeroderma pigmentosum group type C OMIM:278720 XPC XP, Group C xeroderma pigmentosum