autosomal recessive nonsyndromic deafness 23

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 PCDH15 gene on chromosome 10q21.

Signs and symptoms

• Sensorineural hearing impairment
• Visual impairment

Also known as: DFNB23; autosomal recessive deafness 23