# Brugada syndrome 9

> Brugada syndrome that has material basis in heterozygous mutation in the KCND3 gene on chromosome 1p13

**Wikidata**: [Q27164496](https://www.wikidata.org/wiki/Q27164496)  
**Source**: https://4ort.xyz/entity/brugada-syndrome-9


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Transient outward current (I(to)) gain-of-function mutations in the KCND3-encoded Kv4.3 potassium channel and Brugada syndrome
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)