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catecholaminergic polymorphic ventricular tachycardia
Summary
- Definition
- A heart conduction disease characterized by adrenergically induced ventricular tachycardia manifesting as syncope and sudden death during exercise, stress or catecholamine infusion without the presence of structural cardiac abnormalities.
- Super Class
- heart conduction disease monogenic disease
External Links
- Disease Ontology
- DOID:0060674
- Mondo Disease Ontology
- ORDO
- OMIM
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 37 | ACADVL | acyl-CoA dehydrogenase very long chain | |
| 811 | CALR | calreticulin | |
| 1636 | ACE | angiotensin I converting enzyme | |
| 2523 | FUT1 | fucosyltransferase 1 (H blood group) | |
| 2992 | GYG1 | glycogenin 1 | |
| 5067 | CNTN3 | contactin 3 | |
| 5743 | PTGS2 | prostaglandin-endoperoxide synthase 2 | |
| 6319 | SCD | stearoyl-CoA desaturase | |
| 56994 | CHPT1 | choline phosphotransferase 1 | |
| 64083 | GOLPH3 | golgi phosphoprotein 3 |
Related Glycoprotein
