Term Name:	autosomal recessive nonsyndromic deafness 22
Synonyms:	autosomal recessive deafness 22, DFNB22
Definition:	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.
Ontology:	Human Disease [DOID:0110480]   ( DOID:0110480 )