Long Qt Syndrome 15; Lqt15

Clinical Features

Top most frequent phenotypes and symptoms related to Long Qt Syndrome 15; Lqt15

  • Seizures
  • Arrhythmia
  • Syncope
  • Bradycardia
  • Cardiac arrest
  • Spontaneous abortion
  • Ventricular fibrillation
  • Sinus bradycardia
  • Abnormal T-wave
  • Prolonged QTc interval

And another 1 symptoms. If you need more information about this disease we can help you.

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Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
No data available about the known clinical features onset.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.


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Long Qt Syndrome 15; Lqt15 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Comprehensive Cardiac Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).

RIT1, RYR2, SCN1B, SCN2B, SCN4B, SCN5A, SGCD, SLC22A5, BRAF, SNTA1, SOS1, TAZ, TCAP, TGFB3, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TTN , (...)

View the complete list with 86 more genes
Specificity
1 %
Genes
100 %
Long QT Syndrome Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).

RYR2, SCN4B, SCN5A, SNTA1, TRDN, CACNA1C, CALM1, CALM2, CASQ2, CAV3, AKAP9, ANK2, KCNE1, KCNE2, KCNH2, KCNJ2, KCNJ5, KCNQ1
Specificity
6 %
Genes
100 %
LQTS panel.

By Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS (Italy).

SCN4B, SCN5A, CACNA1C, CALM1, CALM2, CAV3, AKAP9, ANK2, KCNE1, KCNE2, KCNH2, KCNJ2, KCNQ1
Specificity
8 %
Genes
100 %
CALM2.

By Institute for Human Genetics University Clinic Freiburg (Germany).

CALM2
Specificity
100 %
Genes
100 %
Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam (Netherlands).

RYR2, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, SNTA1, TNNT2, TRDN, CACNA1C, CACNA1D, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, SLMAP, HCN4 , (...)

View the complete list with 27 more genes
Specificity
3 %
Genes
100 %
Long QT Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

SCN4B, SCN5A, SNTA1, CACNA1C, CALM1, CALM2, CAV3, AKAP9, ANK2, KCNE1, KCNE2, KCNH2, KCNJ2, KCNJ5, KCNQ1
Specificity
7 %
Genes
100 %
Long QT Syndrome via CALM2 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

CALM2
Specificity
100 %
Genes
100 %
Comprehensive Cardiac Arrhythmia Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RYR2, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, SNTA1, TGFB3, TNNI3, TRDN, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, LDB3, SLMAP , (...)

View the complete list with 35 more genes
Specificity
2 %
Genes
100 %

We have 47 more panels available in our App

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Sources and references

You can check the following sources for additional information.

OMIM Genetic Syndrome Finder

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