Human genes for autosomal dominant nonsyndromic deafness 50
Autosomal dominant nonsyndromic deafness 50 [DOID:0110576]
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.
Synonyms: autosomal dominant nonsyndromic deafness 50, DOID:0110576, autosomal dominant deafness 50, DFNA50