autosomal dominant nonsyndromic deafness 49

An autosomal dominant nonsyndromic deafness that is characterized by moderate loss for low and mid frequencies and mild loss for high frequencies and has_material_basis_in variation in the chromosome region 1q21-q23.

Signs and symptoms

• Sensorineural hearing impairment
• Progressive hearing impairment

Also known as: DFNA49; autosomal dominant deafness 49