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Brugada syndrome 9

Disease Summary
Associated Targets (1)
Tclin

1


Mondo Description Any Brugada syndrome in which the cause of the disease is a mutation in the KCND3 gene.
Uniprot Description A tachyarrhythmia characterized by right bundle branch block and ST segment elevation on an electrocardiogram (ECG). It can cause the ventricles to beat so fast that the blood is prevented from circulating efficiently in the body. When this situation occurs, the individual will faint and may die in a few minutes if the heart is not reset.
Disease Ontology Description A Brugada syndrome that has material basis in heterozygous mutation in the KCND3 gene on chromosome 1p13.
Mondo Term and Equivalent IDs
MONDO:0014621:  Brugada syndrome 9
UMLS:C4225340: