autosomal recessive nonsyndromic deafness 49

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, stable hearing loss and has_material_basis_in mutation in the MARVELD2 gene on chromosome 5q13.

Signs and symptoms

• Prelingual sensorineural hearing impairment

Also known as: DFNB49; autosomal recessive deafness 49