autosomal recessive nonsyndromic deafness 36

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the ESPN gene on chromosome 1p36.

Signs and symptoms

• Sensorineural hearing impairment
• Vestibular areflexia

Also known as: DFNB36; autosomal recessive deafness 36