Dyschromatosis symmetrica hereditaria

Definition

A rare genodermatosis characterised by the presence of hyperpigmented and hypopigmented macules, principally located on the extremities and limbs.

Disease data

Classification

Disease

Synonyms

Acropigmentation of Dohi

ORPHA code

OMIM code

127400

ICD10 code

L81.8

ICD11 code

*Soruce

No additional description.

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Description of the disease *