autosomal recessive nonsyndromic deafness 16

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 STRC gene on chromosome 15q15.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNB16; autosomal recessive deafness 16