disease has basis in disruption of disease caused by disruption of UV-damage excision repair progeroid syndrome hereditary photodermatosis xeroderma pigmentosum https://github.com/monarch-initiative/mondo/issues/1567 https://rarediseases.info.nih.gov/diseases/7910/xeroderma-pigmentosum MEDGEN:21943 Orphanet:910 NORD:1870 angioma pigmentosum atrophicum Kaposi disease icd11.foundation:1243068849 NANDO:1200608 melanosis lenticularis progressiva MONDO:0019600 MedDRA:10048220 pigmented epitheliomatosis SCTID:44600005 Xeroderma pigmentosum (XP) is a rare genodermatosis characterized by extreme sensitivity to ultraviolet (UV)-induced changes in the skin and eyes, and multiple skin cancers. It is subdivided into 8 complementation groups, according to the affected gene: classical XP (XPA to XPG) and XP variant (XPV). xeroderma of Kaposi DOID:0050427 NANDO:2100286 xeroderma pigmentosum syndrome xeroderma pigmentosa MESH:D014983 NANDO:2201002 ICD10CM:Q82.1 Kaposi dermatosis OMIMPS:278700 UMLS:C0043346 GARD:0007910 XP NCIT:C3452 atrophoderma pigmentosum DNA repair disease