# long QT syndrome 3

> long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SCN5A gene on chromosome 3p22.2

**Wikidata**: [Q32139750](https://www.wikidata.org/wiki/Q32139750)  
**Source**: https://4ort.xyz/entity/long-qt-syndrome-3


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21.
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000183873/MONDO_0011377)
6. [Identifiers.org](https://registry.identifiers.org/registry/doid)