autosomal recessive nonsyndromic deafness 30

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutations in the MYO3A gene on chromosome 10p12.1.

Signs and symptoms

• Progressive sensorineural hearing impairment
• Progressive hearing impairment

Also known as: DFNB30; autosomal recessive deafness 30