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Brugada syndrome 5
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any Brugada syndrome in which the cause of the disease is a mutation in the SCN1B 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.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0110222
OMIM:612838
UMLS:C2748541
MONDO:0013015
High level summary of knowledge for a disease, including descriptions and datasource references.