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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](img/icons/info1.png)
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