autosomal recessive nonsyndromic deafness 32 (DOID:0110491)
Alliance: disease page
Synonyms: autosomal recessive deafness 32; autosomal recessive deafness 105; DFNB32; hearing impairment infertile male syndrome; HIIMS
Alt IDs: OMIM:608653, ICD10CM:H90.3
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and male infertility in some affected men that has_material_basis_in mutation in the CDC14A gene on chromosome 1p21.2.