autosomal dominant nonsyndromic deafness 6

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.

Signs and symptoms

• Progressive sensorineural hearing impairment
• Low-frequency sensorineural hearing impairment

Also known as: DFNA14; DFNA38; DFNA6; DFNA6/14/38; autosomal dominant deafness 14