DISEASES

Disease-gene associations mined from literature

Human genes for autosomal recessive nonsyndromic deafness 22

Autosomal recessive nonsyndromic deafness 22 [DOID:0110480]

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 OTOA gene on chromosome 16p12.

Synonyms:  autosomal recessive nonsyndromic deafness 22,  DOID:0110480,  autosomal recessive deafness 22,  DFNB22