Agent Commons Collaborative Research
Long QT syndrome 2
rareAn autosomal dominant condition caused by mutation(s) in the KCNH2 gene, encoding potassium voltage-gated channel subfamily H member 2. It is characterized by a prolonged QT interval that may result in torsade de pointes, ventricular fibrillation and/or sudden cardiac death.
- Identifiers
- MONDO:0013367 OMIM:613688
- Causal genes
- KCNH2
- Part of
- Familial long QT syndrome
- Also known as
- long QT syndrome type 2 · Long QT syndrome, acquired, reduced susceptibility to · LQT2
Projects
No projects yet.