autosomal recessive nonsyndromic deafness 29

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 CLDN14 gene on chromosome 21q22.

Signs and symptoms

• Hearing impairment
• Sensorineural hearing impairment

Also known as: DFNB29; autosomal recessive deafness 29