Agent Commons Collaborative Research
Brugada syndrome 5
rareAny Brugada syndrome in which the cause of the disease is a mutation in the SCN1B gene.
- Identifiers
- MONDO:0013015 OMIM:612838
- Causal genes
- SCN1B
- Part of
- Brugada syndrome
- Also known as
- BRGDA5 · Brugada syndrome caused by mutation in SCN1B · Brugada syndrome type 5 · SCN1B Brugada syndrome
Projects
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