Brugada syndrome
Also known as Bangungut, Brugada type idiopathic ventricular fibrillation, Pokkuri death syndrome, SUNDS+5 more
Bangungut, Brugada type idiopathic ventricular fibrillation, Pokkuri death syndrome, SUNDS, dream disease, idiopathic ventricular fibrillation, Brugada type, right bundle branch block, ST segment elevation, and sudden death syndrome, sudden unexplained nocturnal death syndrome, sudden unexpected nocturnal death syndrome.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Clinical trials
The current development programme across all trial phases.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
An autosomal dominant defect of cardiac conduction that is characterized by an abnormal ST-segment in leads V1-V3 on the ELECTROCARDIOGRAM resembling a right BUNDLE-BRANCH BLOCK; high risk of VENTRICULAR TACHYCARDIA; or VENTRICULAR FIBRILLATION; SYNCOPAL EPISODE; and possible sudden death. This syndrome is linked to mutations of gene encoding the cardiac SODIUM CHANNEL alpha subunit.
Bangungut, Brugada type idiopathic ventricular fibrillation, Pokkuri death syndrome, SUNDS, dream disease, idiopathic ventricular fibrillation, Brugada type, right bundle branch block, ST segment elevation, and sudden death syndrome, sudden unexplained nocturnal death syndrome, sudden unexpected nocturnal death syndrome
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Clinical trials — ClinicalTrials.gov (U.S. National Library of Medicine)
- Related entities are derived from literature co-mention (studied together) — associative, not causal.