Human genes for autosomal dominant nonsyndromic deafness 10
Autosomal dominant nonsyndromic deafness 10 [DOID:0110542]
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the third or forth decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the EYA4 gene on chromosome 6q23.
Synonyms: autosomal dominant nonsyndromic deafness 10, DOID:0110542, autosomal dominant deafness 10, DFNA10