autosomal recessive nonsyndromic deafness 7

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 TMC1 gene on chromosome 9q21.

Signs and symptoms

• Sensorineural hearing impairment
• Abnormal vestibular function

Also known as: DFNB11; DFNB7; autosomal recessive deafness 7