Wolfram syndrome, mitochondrial form

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Summary

Literature (0)

DOID:0080583 - Wolfram syndrome, mitochondrial form

Disease Ontology Definition:A Wolfram syndrome that has_material_basis_in mutation in mtDNA.

Synonyms: DIDMOAD, mitochondrial form, diabetes mellitus AND insipidus with optic atrophy AND deafness mitochondrial form,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): Wolfram syndrome (is_a)