DISEASES

Disease-gene associations mined from literature

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