Brugada syndrome 9

Summary
Synonym
  • BRGDA9
Definition
A Brugada syndrome that has_material_basis_in heterozygous mutation in the KCND3 gene on chromosome 1p13.
Super Class
Brugada syndrome autosomal dominant disease
Disease Ontology
DOID:0110226
Mondo Disease Ontology
OMIM
The Human Phenotype Ontology
Displaying entries 11 - 12 of 12 in total
HPO ID HPO Term
HP:0001663 Ventricular fibrillation
HP:0004755 Supraventricular tachycardia
Displaying all 2 entries
Gene ID Gene Symbol Description
23171 GPD1L glycerol-3-phosphate dehydrogenase 1 like
781 CACNA2D1 calcium voltage-gated channel auxiliary subunit alpha2delta 1

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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