autosomal dominant nonsyndromic deafness 4A

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently sloping hearing audioprofiles and has_material_basis_in mutation in the MYH14 gene on chromosome 19q13.33.

Signs and symptoms

• Progressive sensorineural hearing impairment

Also known as: DFNA4A; autosomal dominant deafness 4A