autosomal dominant nonsyndromic deafness 22

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.

Signs and symptoms

• Progressive sensorineural hearing impairment
• Sensorineural hearing impairment

Also known as: DFNA22; autosomal dominant deafness 22