autosomal-mitochondrial sensorineural deafness Disease Ontology Browser

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Disease Ontology Browser

autosomal-mitochondrial sensorineural deafness (DOID:0111752)
Alliance: disease page
Alt IDs: OMIM:221745
Definition: A sensorineural hearing loss characterized by progressive, severe to profound deafness that has_material_basis_in digenic inheritance of mutations in the mitochondrial gene MTRNR1 and an unidentified nuclear gene.

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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