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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 : abcb6


OMIM:
MIM:615402 - dyschromatosis universalis hereditaria 3; duh3

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)