Term Name:	autosomal-mitochondrial sensorineural deafness
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 )