autosomal recessive nonsyndromic deafness 1B

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12.

Signs and symptoms

• Hearing impairment
• Abnormal vestibular function

Also known as: DFNB1B; autosomal recessive deafness 1B