# Brugada syndrome 5

> Brugada syndrome that has material basis in heterozygous mutation in the SCN1B gene on chromosome 19q13

**Wikidata**: [Q27677687](https://www.wikidata.org/wiki/Q27677687)  
**Source**: https://4ort.xyz/entity/brugada-syndrome-5


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)