Human genes for autosomal recessive nonsyndromic deafness 66
Autosomal recessive nonsyndromic deafness 66 [DOID:0110517]
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the DCDC2 gene on chromosome 6p22.
Synonyms: autosomal recessive nonsyndromic deafness 66, DOID:0110517, autosomal recessive deafness 66, DFNB66