Human genes for autosomal dominant nonsyndromic deafness 40
Autosomal dominant nonsyndromic deafness 40 [DOID:0110566]
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CRYM gene on chromosome 16p12.
Synonyms: autosomal dominant nonsyndromic deafness 40, DOID:0110566, autosomal dominant deafness 40, DFNA40