Long Qt Syndrome
Disease ID: disease_node_4835
Connections displayed (default: 10).
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| Dbxref | 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 |
|---|---|
| Subclassof | DOID_0060036 |
| Data Source | DOID, MESH |
| Synonyms | LQT, long Q-T syndrome, Romano-Ward syndrome |
| Mesh Id | D008133 |
| Mesh Label | Long QT Syndrome |
| Mesh Subclassof | D006330, D001145, D000075224 |
| Doid Label | long QT syndrome |
| Doid Description | 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). OMIM mapping confirmed by DO. [SN]. |
| Has Symptom | SYMP_0000287 |
| Disease Node Id | disease_node_4835 |
| Doid Id | DOID_2843 |
| Label | Long Qt Syndrome |
| Doid Alternate Ids | DOID_4069 |
- Outgoing r'ship
HAS_SYMPTOMto/from Arrhythmia(ID:disease_node_21133) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Long Qt Syndrome 16(ID:disease_node_16875) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Long Qt Syndrome 1(ID:disease_node_16880) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Long Qt Syndrome 8(ID:disease_node_16879) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Long Qt Syndrome 14(ID:disease_node_16877) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Long Qt Syndrome 13(ID:disease_node_16878) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Long Qt Syndrome 15(ID:disease_node_16876) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Intrinsic Cardiomyopathy(ID:disease_node_16869) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Jervell-Lange Nielsen Syndrome(ID:disease_node_11031) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Andersen Syndrome(ID:disease_node_11420) (Disease)