autosomal recessive nonsyndromic deafness 32

Term ID

DOID:0110491

Synonyms

• autosomal recessive deafness 32
• DFNB32
• hearing impairment infertile male syndrome
• HIIMS

(all 4)

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. (2)

References

• ICD10CM:H90.3
• MIM:608653

Ontology

Human Disease   ( DOID:0110491 )