Human genes for autosomal dominant nonsyndromic deafness 25
Autosomal dominant nonsyndromic deafness 25 [DOID:0110555]
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second-sixth decade of life with high frequency progressive hearing loss and has_material_basis_in mutation in the SLC17A8 gene on chromosome 12q23.
Synonyms: autosomal dominant nonsyndromic deafness 25, DOID:0110555, autosomal dominant deafness 25, DFNA25