# Brugada syndrome 4

> Brugada syndrome that has material basis in heterozygous mutation in the gene encoding the beta-2 subunit of the voltage-dependent L-type calcium channel (CACNB2) on chromosome 10p12

**Wikidata**: [Q27677685](https://www.wikidata.org/wiki/Q27677685)  
**Source**: https://4ort.xyz/entity/brugada-syndrome-4


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)