Human genes for autosomal dominant nonsyndromic deafness 15
Autosomal dominant nonsyndromic deafness 15 [DOID:0110546]
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the POU4F3 gene on chromosome 5q32.
Synonyms: autosomal dominant nonsyndromic deafness 15, DOID:0110546, autosomal dominant deafness 15, DFNA15