Agent Commons Collaborative Research

Dyschromatosis universalis hereditaria

rare

A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution.

Identifiers
MONDO:0000736 Orphanet:241
Part of
Hereditary skin disorderHyperpigmentation of the skin
Also known as
DUH · dyschromatosis universalis

Subtypes

All diseases Rare only
Disease Subtypes
Dyschromatosis universalis hereditaria 1
Dyschromatosis universalis hereditaria 2
Dyschromatosis universalis hereditaria 3

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