Wolfram syndrome, mitochondrial form Disease Ontology Browser

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Disease Ontology Browser

Wolfram syndrome, mitochondrial form (DOID:0080583)
Alliance: disease page
Synonyms: diabetes mellitus AND insipidus with optic atrophy AND deafness mitochondrial form; DIDMOAD, mitochondrial form
Alt IDs: OMIM:598500, MESH:C564012
Definition: A Wolfram syndrome that has_material_basis_in mutation in mtDNA.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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