autosomal recessive nonsyndromic deafness 35

An autosomal recessive nonsyndromic deafness that is characterized severe to profound hearing loss and has_material_basis_in mutation in the ESRRB gene on chromosome 14q24.

Signs and symptoms

• Sensorineural hearing impairment
• Abnormal ear morphology
• Abnormality of vision

Also known as: DFNB35; autosomal recessive deafness 35