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short QT syndrome
Summary
- Definition
- A 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.
- Super Class
- heart conduction disease
External Links
- Disease Ontology
- DOID:0050793
- MGI genotype (from TogoID)
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P51787 | Potassium voltage-gated channel subfamily KQT member 1 | |
| Q12809 | Voltage-gated inwardly rectifying potassium channel KCNH2 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| O35219 | Voltage-gated inwardly rectifying potassium channel KCNH2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001663 | Ventricular fibrillation |
| HP:0005110 | Atrial fibrillation |
| HP:0001645 | Sudden cardiac death |
| HP:0001962 | Palpitations |
| HP:0001279 | Syncope |
| HP:0004308 | Ventricular arrhythmia |
| HP:0001662 | Bradycardia |
| HP:0012232 | Shortened QT interval |
| HP:0001678 | Atrioventricular block |
