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Summary Literature (23)
DOID:2843 - long QT syndrome

Disease Ontology 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).

Synonyms: LQT, Romano-Ward syndrome, Romano-Ward syndrome (disorder), long Q-T syndrome

Referenced OMIM:

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : scn4b, kcne1, snta1, cav3.1, kcnj2, cav3.2, kcnj5, kcnq1, akap9, scn5a

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): intrinsic cardiomyopathy (is_a)

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Version: 4.14.0
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