loading...| Preferred Name |
long QT syndrome |
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| Synonyms |
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| 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]. |
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| ID |
http://purl.obolibrary.org/obo/DOID_2843 |
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| comment |
OMIM mapping confirmed by DO. [SN]. |
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| 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). |
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| hasAlternativeId |
DOID:4069 |
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| hasDbXref |
ICD9CM:426.82 ICD10CM:I45.81 UMLS_CUI:C0023976 SNOMEDCT_US_2016_03_01:9651007 MESH:D008133 NCI:C85049 NCI:C34786 MESH:D029597 UMLS_CUI:C0035828 SNOMEDCT_US_2016_03_01:20852007 SNOMEDCT_US_2016_03_01:395649008 |
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| hasExactSynonym |
long Q-T syndrome LQT Romano-Ward syndrome (disorder) Romano-Ward syndrome |
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| hasOBONamespace |
disease_ontology |
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| id |
DOID:2843 |
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| imported from | ||
| inSubset | ||
| label |
long QT syndrome |
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| prefixIRI |
DOID:2843 |
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| prefLabel |
long QT syndrome |
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| subClassOf |
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