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Digital medicine Outcomes Value Set (DOVeS) Ontology
Last uploaded:
December 13, 2023
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| Preferred Name | long QT syndrome | |
| Synonyms |
long Q-T syndrome LQT long QT syndrome ventricular arrhythmia associated with long QT syndrome |
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| Definitions |
A condition that is characterized by episodes of fainting (syncope) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Romano-Ward syndrome (also known as long QT syndrome 1) and Jervell-Lange Nielsen syndrome. |
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| ID |
http://purl.obolibrary.org/obo/MONDO_0002442 |
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| altLabel |
long Q-T syndrome LQT long QT syndrome ventricular arrhythmia associated with long QT syndrome
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| definition |
A condition that is characterized by episodes of fainting (syncope) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Romano-Ward syndrome (also known as long QT syndrome 1) and Jervell-Lange Nielsen syndrome.
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| disease has feature | ||
| has_exact_synonym |
long Q-T syndrome LQT long QT syndrome ventricular arrhythmia associated with long QT syndrome
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| label |
long QT syndrome
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| prefixIRI |
MONDO:0002442
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| prefLabel |
long QT syndrome
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| textual definition |
A condition that is characterized by episodes of fainting (syncope) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are Romano-Ward syndrome (also known as long QT syndrome 1) and Jervell-Lange Nielsen syndrome.
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| subClassOf |
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