| congenitaal lang-QT-intervalsyndroom (aandoening) | | congenitaal lang-QT-intervalsyndroom | | congenitaal lang-QT-syndroom
congenitaal LQTS
| | Familial long QT syndrome | | Inherited long QT syndrome
Congenital long QT syndrome
| | A rare group of genetic, cardiac rhythm diseases with characteristics of a prolongation of the QT interval at basal electrocardiography (ECG) and by a high risk of life-threatening arrhythmias. The two cardinal manifestations are syncopal episodes, which may lead to cardiac arrest and sudden cardiac death, and electrocardiographic abnormalities: prolongation of the QT interval and T wave abnormalities. Inheritance may be autosomal dominant or autosomal recessive and depends on the genes involved. |
| | SNOMED CT to Orphanet simple map | 768 |
| SNOMED CT to ICD-10 extended map | | Target | I49.8 | | Rule | TRUE | | Advice | ALWAYS I49.8 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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