autosomal recessive nonsyndromic deafness 18A

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the USH1C gene on chromosome 11p15.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNB18A; autosomal recessive deafness 18A