Dyschromatosis universalis hereditaria

Orpha code: 241OMIM code: 615402

Definicja

A rare, genetic, pigmentation anomaly of the skin characterized by generalized, irregularly shaped, asymptomatic, hyper- and hypopigmented macules distributed in a reticular pattern involving the trunk, limbs, and sometimes the face. The palms, soles and mucosa are usually not affected. Systemic abnormalities have been rarely reported.

Disease data
Klasyfikacja

Disease

Kod ORPHA
241
Kod OMIM
615402
Kod ICD10
L81.8
Kod ICD11
-

No additional description.

Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl