DISEASES

Disease-gene associations mined from literature

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