autosomal recessive nonsyndromic deafness 31

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the WHRN gene on chromosome 9q32.

Signs and symptoms

• Sensorineural hearing impairment
• Absent vestibular function

Also known as: DFNB31; autosomal recessive deafness 31