autosomal dominant nonsyndromic deafness 12

An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNA12; DFNA8; autosomal dominant deafness 12; autosomal dominant deafness 8