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.
Finding sitestructuur van hart
Global Patient Set
SNOMED CT to Orphanet simple map768
SNOMED CT to ICD-10 extended map
AdviceALWAYS I49.8
CorrelationSNOMED CT source code to target map code correlation not specified