autosomal recessive nonsyndromic deafness 61

An autosomal recessive nonsyndromic deafness that is characterized by early childhood-onset moderate to severe sensorineural hearing loss and has_material_basis_in mutation in the SLC26A5 gene on chromosome 7q22.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNB61; autosomal recessive deafness 61