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congenital heart disease (MONDO:0005453)
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syndromic disease (MONDO:0002254)
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long QT syndrome ()

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Further data from MedGen, OMIM,ClinVar, CTD
Term ID:2442
Name:long QT syndrome
Definition:A condition that is characterized by episodes of fainting (syncope) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Romano-Ward syndrome and Jervell-Lange Nielsen syndrome.
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Synonyms:long Q-T syndrome; LQT; Romano-Ward syndrome; ventricular arrhythmia associated with long QT syndrome
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