autosomal dominant nonsyndromic deafness 13

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has_material_basis_in mutation in the COL11A2 gene on chromosome 6p21.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNA13; autosomal dominant deafness 13