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
External Links
Disease Ontology
DOID:2843
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
Related Genes
Displaying entries 1 - 10 of 11 in total
Gene ID Gene Symbol Description Source
34 ACADM acyl-CoA dehydrogenase medium chain
1543 CYP1A1 cytochrome P450 family 1 subfamily A member 1
3784 KCNQ1 potassium voltage-gated channel subfamily Q member 1
5067 CNTN3 contactin 3
5728 PTEN phosphatase and tensin homolog
6319 SCD stearoyl-CoA desaturase
6518 SLC2A5 solute carrier family 2 member 5
6713 SQLE squalene epoxidase
23205 ACSBG1 acyl-CoA synthetase bubblegum family member 1
84920 ALG10 ALG10 alpha-1,2-glucosyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
16535 Kcnq1 potassium voltage-gated channel, subfamily Q, member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
84020 Kcnq1 potassium voltage-gated channel subfamily Q member 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024