Human genes for autosomal dominant nonsyndromic deafness 4B
Autosomal dominant nonsyndromic deafness 4B [DOID:0110574]
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CEACAM16 gene on chromosome 19q13.
Synonyms: autosomal dominant nonsyndromic deafness 4B, DOID:0110574, autosomal dominant deafness 4B, DFNA4B