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Echinobase
Summary Literature (0)
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,

Echinobase Genes :


OMIM:
MIM:127400 - dyschromatosis symmetrica hereditaria; dsh

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)