|
DOID:0060257 - dyschromatosis symmetrica hereditaria
Disease Ontology Definition:A pigmentation disease characterized by progressively pigmented and depigmented macules, often mixed in a reticulate pattern, concentrated on the dorsal extremities.
Synonyms: reticulate acropigmentation of Dohi
Xenbase Genes : adar
MONDO:0007483 - dyschromatosis symmetrica hereditaria |
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)