Term Name:	autosomal dominant nonsyndromic deafness 12
Synonyms:	autosomal dominant deafness 12, autosomal dominant deafness 8, DFNA12, DFNA8
Definition:	An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and mid-frequency hearing loss and has_material_basis_in mutation in the TECTA gene on chromosome 11q23.
Ontology:	Human Disease [DOID:0110544]   ( DOID:0110544 )