autosomal recessive nonsyndromic deafness 120

An autosomal recessive nonsyndromic deafness characterized by congenital or prelingual onset of severe to profound sensorineural hearing loss that has_material_basis_in homozygous mutation in the MINAR2 gene on chromosome 5q23.

Signs and symptoms

• Sensorineural hearing impairment

Also known as: DFNB120