dyschromatosis universalis hereditaria

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Echinobase

Summary

Literature (0)

DOID:0060304 - dyschromatosis universalis hereditaria

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

Synonyms:

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: abcb6

MIM:

MIM:615402 - dyschromatosis universalis hereditaria 3; duh3

MIM:615402 - dyschromatosis universalis hereditaria 3; duh3

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): pigmentation disease (is_a)