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DO Term : dyschromatosis universalis hereditaria [DOID:0060304] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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

synonyms:
MESH:C535730,
GARD:1996,
ORDO:241,
NCI:C173131,
UMLS_CUI:C2930995,
615402,
OMIM:615402,
OMIM:612715,
127500,
612715,
OMIM:127500

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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