autosomal dominant nonsyndromic deafness 69

An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DCUA; DFNA69; autosomal dominant deafness 69; unilateral or asymmetric congenital deafness