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