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DOID:0060304 - dyschromatosis universalis hereditaria
Disease Ontology Definition:A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution.
Synonyms:
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0000736 - dyschromatosis universalis hereditaria |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
pigmentation disease (is_a)