Human genes for autosomal dominant nonsyndromic deafness 12
Autosomal dominant nonsyndromic deafness 12 [DOID:0110544]
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.
Synonyms: autosomal dominant nonsyndromic deafness 12, DOID:0110544, autosomal dominant deafness 12, autosomal dominant deafness 8, DFNA12 ...