Human genes for autosomal dominant nonsyndromic deafness 6
Autosomal dominant nonsyndromic deafness 6 [DOID:0110584]
An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has_material_basis_in mutation in the WFS1 gene on chromosome 4p16.
Synonyms: autosomal dominant nonsyndromic deafness 6, DOID:0110584, autosomal dominant deafness 14, autosomal dominant deafness 38, autosomal dominant deafness 6 ...