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long QT syndrome
Summary
- Synonym
-
- LQT
- long Q-T syndrome
- Definition
- An autosomal genetic disease that is characterized by delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsade de pointes (TDP, a form of irregular heartbeat that originates from the ventricles).
- Super Class
- intrinsic cardiomyopathy
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 287 | ANK2 | ankyrin 2 | |
| 3753 | KCNE1 | potassium voltage-gated channel subfamily E regulatory subunit 1 | |
| 3757 | KCNH2 | potassium voltage-gated channel subfamily H member 2 | |
| 3784 | KCNQ1 | potassium voltage-gated channel subfamily Q member 1 | |
| 6331 | SCN5A | sodium voltage-gated channel alpha subunit 5 | |
| 9992 | KCNE2 | potassium voltage-gated channel subfamily E regulatory subunit 2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9Z0N7 | Potassium voltage-gated channel subfamily KQT member 1 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| G5EFJ9 | Potassium voltage-gated channel unc-103 |
