autosomal recessive nonsyndromic deafness 37

Summary
Synonym
  • DFNB37
  • autosomal recessive deafness 37
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14.
Super Class
autosomal recessive nonsyndromic deafness
Disease Ontology
DOID:0110495
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

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.1.0

Last updated: December 9, 2024