Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (37)
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,

Xenbase Genes : scn4b, kcne1, snta1, cav3.1, alg10, calm1, kcnh2, ank2, kcnj2, calm2, cav3.2, kcnj5, kcnq1, akap9, scn5a, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0002442 - long QT syndrome

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): intrinsic cardiomyopathy (is_a)