# catecholaminergic polymorphic ventricular tachycardia 5

> catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has material basis in homozygous or compound heterozygous mutation in the TRDN gene on chromosome 6q22

**Wikidata**: [Q28024498](https://www.wikidata.org/wiki/Q28024498)  
**Source**: https://4ort.xyz/entity/catecholaminergic-polymorphic-ventricular-tachycardia-5


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human
5. [Identifiers.org](https://registry.identifiers.org/registry/doid)