DISEASES

Disease-gene associations mined from literature

Human genes for autosomal dominant nonsyndromic deafness 21

Autosomal dominant nonsyndromic deafness 21 [DOID:0110551]

An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 6p24.1-p22.3.

Synonyms:  autosomal dominant nonsyndromic deafness 21,  DOID:0110551,  DFNA21,  autosomal dominant deafness 21