xeroderma pigmentosum
AUTOSOMAL RECESSIVE DISEASE THAT IS CHARACTERIZED BY A DEFICIENCY IN THE ABILITY TO REPAIR ULTRAVIOLET DAMAGE THAT HAS MATERIAL BASIS IN AUTOSOMAL RECESSIVE INHERITANCE OF DNA REPAIR
Xeroderma Pigmentosum; Sunpoisoning; Xeroderma pigmentosa; Xeroderma pigmentosum, complementation group G; Xeroderma pigmentosum group d protein; Xeroderma pigmentosum, type 1; Xeroderma pigmentosum, type 2; Xeroderma pigmentosum, type 3; Xeroderma pigmentosum, type 4; Xeroderma pigmentosum, type 5; Xeroderma pigmentosum, type 6; Xeroderma pigmentosum, type 7; Xeroderma pigmentosum, variant type; Xeroderma pigmentosum type 1; Xeroderma pigmentosum type 2; Xeroderma pigmentosum type 3; Xeroderma pigmentosum type 4; Xeroderma pigmentosum type 5; Xeroderma pigmentosum type 6; Xeroderma pigmentosum type 7; Xeroderma pigmentosum variant type; Xeroderma pigmentosum type I; Xeroderma pigmentosum type II; Xeroderma pigmentosum type III; Xeroderma pigmentosum type IV; Xeroderma pigmentosum type V; Xeroderma pigmentosum type VI; Xeroderma pigmentosum type VII; Xeroderma pigmentosum I; Xeroderma pigmentosum II; Xeroderma pigmentosum III; Xeroderma pigmentosum IV; Xeroderma pigmentosum V; Xeroderma pigmentosum VI; Xeroderma pigmentosum VII; XP1; XP3; XP4; XP5; XP6; XP7; Xeroderma pigmentosum with normal DNA repair rates; Xeroderma pigmentosum group A; Xeroderma pigmentosum group B; Xeroderma pigmentosum group C; Xeroderma pigmentosum group D; Xeroderma pigmentosum group E; Xeroderma pigmentosum group F; Xeroderma pigmentosum group G; Allergy to light; Light allergy; Allergic to light; XPV; Cerebrooculofacioskeletal syndrome 3; Cockayne syndrome complex; Xeroderma pigmentosum, complementation group c; Xeroderma pigmentosum-Cockayne syndrome; Xeroderma pigmentosum–Cockayne syndrome; DDB2-Related Xeroderma Pigmentosum; Moon children
n. xeroderma pigmentosum, rara malattia genetica della pelle caratterizzata da una estrema fotosensibilità alla luce ultravioletta (medic.)