autosomal recessive nonsyndromic deafness 21

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 TECTA gene on chromosome 11q23.3.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNB21; autosomal recessive deafness 21