Acromelanosis

Orpha code: 39OMIM code:

Definicja

A rare pigmentation anomaly of the skin characterized by otherwise asymptomatic hyperpigmentation of the skin over the dorsal side of fingers and toes which may rapidly spread towards proximal regions, like genitals, abdomen, and thighs. It is mostly seen in newborns or during the first years of life.

Disease data
Klasyfikacja

Disease

Kod ORPHA
39
Kod OMIM
-
Kod ICD10
L81.4
Kod ICD11
-

No additional description.

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