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Disease Ontology Browser
dyschromatosis universalis hereditaria (DOID:0060304)
Alliance: disease page
Alt IDs: OMIM:127500, OMIM:612715, OMIM:615402, MESH:C535730, ORDO:241, UMLS_CUI:C2930995
Definition: A pigmentation disease characterized by reticulate hyper- and hypo-pigmentated macules in a generalized distribution.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.11
The Jackson Laboratory