autosomal recessive nonsyndromic deafness 63

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 LRTOMT gene on chromosome 11q13.

Signs and symptoms

• Congenital sensorineural hearing impairment
• Abnormal vestibular function
• Abnormal fundus morphology

Also known as: DFNB63; autosomal recessive deafness 63