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