autosomal recessive nonsyndromic deafness 22

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 OTOA gene on chromosome 16p12.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNB22; autosomal recessive deafness 22