|
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
:
abcb6
| MONDO:0000736 - dyschromatosis universalis hereditaria |
| MIM:127500 - DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 1; DUH1 |
| MIM:612715 - DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 2; DUH2 |
| 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)