Human genes for autosomal dominant nonsyndromic deafness 44
Autosomal dominant nonsyndromic deafness 44 [DOID:0110569]
An autosomal dominant nonsyndromic deafness that is characterized postlingual onset with low to mild frequency progressive hearing loss and has_material_basis_in mutation in the CCDC50 gene on chromosome 3q28.
Synonyms: autosomal dominant nonsyndromic deafness 44, DOID:0110569, autosomal dominant deafness 44, DFNA44