DISEASES

Disease-gene associations mined from literature

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,  DFNA11,  autosomal dominant deafness 11