autosomal dominant nonsyndromic deafness 36

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the TMC1 gene on chromosome 9q21.

Signs and symptoms

• Sensorineural hearing impairment
• Tinnitus

Also known as: DFNA36; autosomal dominant deafness 36