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DOID:0050793 - short QT syndrome
Disease Ontology Definition:A heart conduction disease that is characterized by heart arrhythmia defined as a short QT interval on an EKG (less than 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart.
Synonyms:
Xenbase Genes
:
cacna2d1,
kcnh2,
kcnj2,
kcnq1
| MONDO:0000453 - short QT syndrome |
| MIM:609620 - SHORT QT SYNDROME 1; SQT1 |
| MIM:609621 - SHORT QT SYNDROME 2; SQT2 |
| MIM:609622 - SHORT QT SYNDROME 3; SQT3 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
heart conduction disease (is_a)