autosomal dominant nonsyndromic deafness 50

An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the second decade of life with flat progressive hearing loss and has_material_basis_in mutation in the MIRN96 gene on chromosome 7q32.

Signs and symptoms

• Progressive sensorineural hearing impairment
• Sensorineural hearing impairment
• Progressive hearing impairment
• Tinnitus

Also known as: DFNA50; autosomal dominant deafness 50