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The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.
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Long QT Syndrome Type 2
Long QT Syndrome Type 2
Prevalence:
1/5000
cardiac
Official
·
OMIM:613688
Official
·
ORPHA768
Cardiac arrhythmia syndrome due to KCNH2 gene mutations.
Associated Genes
KCNH2
Potassium Voltage-Gated Channel Subfamily H Member 2
Chromosome 7
Autosomal Dominant