Preferred Label : Xeroderma pigmentosum G;
ICD-11 definition : Xeroderma pigmentosum complementation group G (XPG) is an extremely rare subtype of
xeroderma pigmentosum (XP), a rare photodermatosis predisposing to skin cancers. Clinical
manifestations can vary as some patients present with a mild XP phenotype (UV sensitivity,
hyper- or hypo-pigmented skin lesions and increased incidence of skin cancer) and
others combine symptoms of XP with systemic and neurological manifestations of Cockayne
syndrome (XP/CS complex).;
ICD-11 synonym : XPG - [xeroderma pigmentosum G];
ICD-11 acronym : XPG;
Origin ID : 2086751990;
Automatic exact mappings (from CISMeF team)
Currated CISMeF NLP mapping
Xeroderma pigmentosum complementation group G (XPG) is an extremely rare subtype of
xeroderma pigmentosum (XP), a rare photodermatosis predisposing to skin cancers. Clinical
manifestations can vary as some patients present with a mild XP phenotype (UV sensitivity,
hyper- or hypo-pigmented skin lesions and increased incidence of skin cancer) and
others combine symptoms of XP with systemic and neurological manifestations of Cockayne
syndrome (XP/CS complex).