DISEASES

Disease-gene associations mined from literature

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