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| Term | long QT syndrome | ID (Ontology) | DOID:2843 (Human Disease) |
| 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). | ||
| Also Known As | "long Q-T syndrome" ; "LQT" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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cardiomyopathy |__intrinsic cardiomyopathy |__long QT syndrome 23 rec. |__Andersen-Tawil syndrome 1 rec. |__Jervell-Lange Nielsen syndrome 1 rec. |__long QT syndrome 1 2 rec. |__long QT syndrome 2 3 rec. |__long QT syndrome 3 2 rec. |__long QT syndrome 4 |__long QT syndrome 5 |__long QT syndrome 6 |__long QT syndrome 8 1 rec. |__long QT syndrome 9 |__long QT syndrome 10 |__long QT syndrome 11 1 rec. |__long QT syndrome 12 1 rec. |__long QT syndrome 13 2 rec. |__long QT syndrome 14 8 rec. |__long QT syndrome 15 8 rec. |__long QT syndrome 16 8 rec. |
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| Is a | intrinsic cardiomyopathy | ||
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GARD:6922 ICD10CM:I45.81 ICD9CM:426.82 MESH:D008133 MIM:PS192500 NCI:C34786 ORDO:768 SNOMEDCT_US_2023_03_01:9651007 UMLS_CUI:C0023976 |
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