Human genes for autosomal dominant nonsyndromic deafness 9
Autosomal dominant nonsyndromic deafness 9 [DOID:0110593]
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has_material_basis_in mutation in the COCH gene on chromosome 14q12.
Synonyms: autosomal dominant nonsyndromic deafness 9, DOID:0110593, autosomal dominant deafness 9, DFNA9