Fraser syndrome 2

Summary
Synonym
  • FRASRS2
Definition
A Fraser syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the FREM2 gene on chromosome 13q13.3.
Super Class
Fraser syndrome
Disease Ontology
DOID:0111407
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
341640 FREM2 FRAS1 related extracellular matrix 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
242022 Frem2 Fras1 related extracellular matrix protein 2

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