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, autosomal dominant deafness 28, DFNA28