Human genes for autosomal dominant nonsyndromic deafness 11
Autosomal dominant nonsyndromic deafness 11 [DOID:0110543]
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the MYO7A gene on chromosome 11q13.
Synonyms: autosomal dominant nonsyndromic deafness 11, DOID:0110543, autosomal dominant deafness 11, DFNA11