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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: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)