# Brugada syndrome 2

> Brugada syndrome that has material basis in heterozygous mutation in the GPD1L gene on chromosome 3p22

**Wikidata**: [Q27677683](https://www.wikidata.org/wiki/Q27677683)  
**Source**: https://4ort.xyz/entity/brugada-syndrome-2


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Mutation in glycerol-3-phosphate dehydrogenase 1 like gene (GPD1-L) decreases cardiac Na+ current and causes inherited arrhythmias
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)