Term Name: | autosomal-mitochondrial sensorineural deafness |
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Synonyms: | |
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. |
Ontology: | Human Disease [DOID:0111752] ( DOID:0111752 ) |