# long QT syndrome 12

> long QT syndrome that has_material_basis_in dominant inheritance of mutation in the SNTA1 gene on chromosome 20q11.21

**Wikidata**: [Q32139824](https://www.wikidata.org/wiki/Q32139824)  
**Source**: https://4ort.xyz/entity/long-qt-syndrome-12


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex
5. [Identifiers.org](http://www.ebi.ac.uk/miriam/main/collections/MIR:00000233)