DISEASES

Disease-gene associations mined from literature

Human genes for autosomal dominant nonsyndromic deafness 28

Autosomal dominant nonsyndromic deafness 28 [DOID:0110557]

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the GRHL2 gene on chromosome 8q22.

Synonyms:  autosomal dominant nonsyndromic deafness 28,  DOID:0110557,  DFNA28,  autosomal dominant deafness 28