autosomal dominant nonsyndromic deafness 50 (DOID:0110576)
Alliance: disease page
Synonyms: autosomal dominant deafness 50; DFNA50
Alt IDs: OMIM:613074, ICD10CM:H90.3
Definition: An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the second decade of life with flat progressive hearing loss and has_material_basis_in mutation in the MIRN96 gene on chromosome 7q32.