Brugada syndrome 1
Also known as BRGDA1, Brugada syndrome caused by mutation in SCN5A, Brugada syndrome type 1, SCN5A Brugada syndrome+3 more
BRGDA1, Brugada syndrome caused by mutation in SCN5A, Brugada syndrome type 1, SCN5A Brugada syndrome, Cardiac conduction defect, nonspecific, right bundle branch block, St segment elevation, and sudden death syndrome, sudden unexplained nocturnal death syndrome.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
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.
BRGDA1, Brugada syndrome caused by mutation in SCN5A, Brugada syndrome type 1, SCN5A Brugada syndrome, Cardiac conduction defect, nonspecific, right bundle branch block, St segment elevation, and sudden death syndrome, sudden unexplained nocturnal death syndrome
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.