DISEASES

Disease-gene associations mined from literature

Human genes for autosomal recessive nonsyndromic deafness 29

Autosomal recessive nonsyndromic deafness 29 [DOID:0110487]

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the CLDN14 gene on chromosome 21q22.

Synonyms:  autosomal recessive nonsyndromic deafness 29,  DOID:0110487,  autosomal recessive deafness 29,  DFNB29