autosomal dominant nonsyndromic deafness 5

Summary
Synonym
  • DFNA5
  • autosomal dominant deafness 5
Definition
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life and high frequency progressive hearing loss, and has_material_basis_in heterozygous mutation in the gasdermin E (GSDME) gene on chromosome 7p15.
Super Class
autosomal dominant nonsyndromic deafness
External Links
Disease Ontology
DOID:0110575
Mondo Disease Ontology
OMIM
Related Genes
Displaying entry 11 - 11 of 11 in total
Gene ID Gene Symbol Description Source
340990 OTOG otogelin

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 v4.0.0

Last updated: August 19, 2024