# short QT syndrome

> heart conduction disease that is characterized by heart arrhythmia defined as a short QT interval on an EKG (less than 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart

**Wikidata**: [Q1484058](https://www.wikidata.org/wiki/Q1484058)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Short_QT_syndrome)  
**Source**: https://4ort.xyz/entity/short-qt-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. Freebase Data Dumps. 2013
4. UniProt
5. Sudden death associated with short-QT syndrome linked to mutations in HERG.
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_6b033c3f-04de-4806-a9f3-0b318082b32e-2020-08-03T160000.000Z)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000055118/Orphanet_51083)
8. Mutation in the KCNQ1 gene leading to the short QT-interval syndrome
9. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000053918/Orphanet_51083)
10. A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene
11. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000123700/Orphanet_51083)
12. BabelNet
13. [Identifiers.org](https://registry.identifiers.org/registry/doid)
14. [Source](https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx)
15. [OpenAlex](https://docs.openalex.org/download-snapshot/snapshot-data-format)