autosomal recessive nonsyndromic deafness 32

Summary

DOID:0110491 - autosomal recessive nonsyndromic deafness 32

Disease Ontology 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.

Synonyms: DFNB32, HIIMS, autosomal recessive deafness 105, autosomal recessive deafness 32, hearing impairment infertile male syndrome,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cdc14a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012091 - autosomal recessive nonsyndromic hearing loss 32

MONDO:0012091 - autosomal recessive nonsyndromic hearing loss 32

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive nonsyndromic deafness (is_a)