loading...| Preferred Name | long QT syndrome | |
| Synonyms |
long Q-T syndrome Romano-Ward syndrome LQT |
|
| Definitions |
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]. |
|
| ID |
http://purl.obolibrary.org/obo/DOID_2843 |
|
| comment |
OMIM mapping confirmed by DO. [SN]. |
|
| database_cross_reference |
ICD9CM:426.82 UMLS_CUI:C0035828 MESH:D008133 CSP2005:4009-0053 SNOMEDCT_US_2018_03_01:9651007 MESH:D029597 OMIM:PS192500 ORDO:101016 SNOMEDCT_US_2018_03_01:20852007 UMLS_CUI:C0023976 ICD10CM:I45.81 GARD:6922 NCI:C34786 NCI:C85049 ORDO:768 |
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| fromArticle |
true |
|
| fromILAE |
true |
|
| has exact synonym |
long Q-T syndrome Romano-Ward syndrome LQT |
|
| has_alternative_id |
DOID:4069 |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:2843 |
|
| imported from | ||
| in subset |
http://purl.oboInOwllibrary.org/oboInOwl/doid#NCIthesaurus http://purl.oboInOwllibrary.org/oboInOwl/doid#DO_FlyBase_slim |
|
| label |
long QT syndrome |
|
| notation |
DOID:2843 |
|
| prefLabel |
long QT syndrome |
|
| see also |
https://www.epilepsydiagnosis.org/epilepsy-imitators.html#longqt |
|
| 文本定义 |
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). |
|
| subClassOf |