autosomal recessive nonsyndromic deafness 32

Term ID

DOID:0110491

Synonyms

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

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 )