Human genes for autosomal recessive nonsyndromic deafness 32
Autosomal recessive nonsyndromic deafness 32 [DOID:0110491]
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and male infertility in some affeted men that has_material_basis_in mutation in CDC14A on chromosome 1p21.2.
Synonyms: autosomal recessive nonsyndromic deafness 32, DOID:0110491, autosomal recessive deafness 105, autosomal recessive deafness 32, DFNB32 ...