autosomal dominant nonsyndromic deafness 22

Summary
Synonym
  • DFNA22
  • autosomal dominant deafness 22
Definition
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.
Super Class
autosomal dominant nonsyndromic deafness
Disease Ontology
DOID:0110552
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
4646 MYO6 myosin VI
Displaying 1 entry
Gene ID Gene Symbol Description Source
17920 Myo6 myosin VI

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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: December 9, 2024