autosomal recessive nonsyndromic deafness 37

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.

Signs and symptoms

• Sensorineural hearing impairment
• Abnormal vestibular function
• Early-onset non-progressive night blindness
• Rod-cone dystrophy

Also known as: DFNB37; autosomal recessive deafness 37