autosomal recessive nonsyndromic deafness 3

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 MYO15A gene on chromosome 17p11.

Signs and symptoms

• Profound sensorineural hearing impairment

Also known as: DFNB3; NRSD3; autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3