Human genes for autosomal dominant nonsyndromic deafness 23
Autosomal dominant nonsyndromic deafness 23 [DOID:0110553]
An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the SIX1 gene on chromosome 14q23.
Synonyms: autosomal dominant nonsyndromic deafness 23, DOID:0110553, autosomal dominant deafness 23, DFNA23