autosomal recessive nonsyndromic deafness 32

Summary
Synonym
  • DFNB32
  • HIIMS
  • autosomal recessive deafness 105
  • autosomal recessive deafness 32
  • hearing impairment infertile male syndrome
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.
Super Class
autosomal recessive nonsyndromic deafness
External Links
Disease Ontology
DOID:0110491
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entry 11 - 11 of 11 in total
Gene ID Gene Symbol Description Source
340990 OTOG otogelin

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024