Human genes for autosomal dominant nonsyndromic deafness 49
Autosomal dominant nonsyndromic deafness 49 [DOID:0110572]
An autosomal dominant nonsyndromic deafness that is characterized by moderate loss for low and mid frequencies and mild loss for high frequencies and has_material_basis_in variation in the chromosome region 1q21-q23.
Synonyms: autosomal dominant nonsyndromic deafness 49, DOID:0110572, autosomal dominant deafness 49, DFNA49