# long QT syndrome 14

> long QT syndrome that has material basis in dominant inheritance of mutation in the CALM1 gene on chromosome 14q32.11

**Wikidata**: [Q32139852](https://www.wikidata.org/wiki/Q32139852)  
**Source**: https://4ort.xyz/entity/long-qt-syndrome-14


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. Calmodulin mutations associated with recurrent cardiac arrest in infants
4. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000198668/MONDO_0014548)
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)