exudative vitreoretinopathy 7

Summary
Synonym
  • EVR7
Definition
An exudative vitreoretinopathy that has_material_basis_in heterozygous mutation in the CTNNB1 gene on chromosome 3p22.1.
Super Class
autosomal dominant disease exudative vitreoretinopathy
Disease Ontology
DOID:0080264
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1499 CTNNB1 catenin beta 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
12387 Ctnnb1 catenin beta 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
84353 Ctnnb1 catenin beta 1

About Release Notes Help Feedback

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