autosomal recessive nonsyndromic deafness 39

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21.

Signs and symptoms

• Prelingual sensorineural hearing impairment

Also known as: DFNB39; autosomal recessive deafness 39