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Standards Ontologies Notations
catecholaminergic polymorphic ventricular tachycardia 1

Summary
Synonym
  • CVPT1
  • arrhythmogenic right ventricular dysplasia 2
Definition
A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the RYR2 gene on chromosome 1q43.
Super Class
catecholaminergic polymorphic ventricular tachycardia
Disease Ontology
DOID:0060675
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6262 RYR2 ryanodine receptor 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
20191 Ryr2 ryanodine receptor 2, cardiac
Displaying 1 entry
Gene ID Gene Symbol Description Source
689560 Ryr2 ryanodine receptor 2
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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

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Last updated: December 9, 2024