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Dyschromatosis universalis hereditaria

MONDO:0000736

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

Also known as: dyschromatosis universalis, DUH

9 clinical trials for this condition and its sub-types.

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Sub-types

Dyschromatosis universalis hereditaria 1 (0) Dyschromatosis universalis hereditaria 2 (0) Dyschromatosis universalis hereditaria 3 (0)

Broader categories

Disease (618) Hereditary disease (172) Skin disorder (123) Human disease (14) Hyperpigmentation of the skin (11) Skin pigmentation disorder (11) Hereditary skin disorder (5) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)
Trials to join now! 4 Not yet recruiting 2 Not yet finished but already full! 1 Completed 2
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