atriale tachycardie
autosomaal dominante hereditaire aandoening
cardiale aritmie geassocieerd met genetische aandoening
familiaire aandoening
hereditaire aandoening van cardiovasculair systeem
tachyaritmie
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familiaire atriale tachyaritmie met hartprikkelgeleidingsstoornis in of onder bundel van His (aandoening)
familiaire atriale tachyaritmie met hartprikkelgeleidingsstoornis in of onder bundel van His
familiaire atriale tachyaritmie met hartblok in of onder atrioventriculaire bundel
familiaire atriale tachyaritmie met hartgeleidingsdefect in of onder bundel van His
familiaire atriale tachyaritmie met cardiale geleidingsstoornis in of onder fasciculus atrioventricularis
Familial atrial tachyarrhythmia, infra-Hisian cardiac conduction disease
A rare genetic cardiac disease characterized by variably expressed atrial tachyarrhythmia (such as atrial flutter, paroxysmal or chronic atrial fibrillation, ectopic atrial tachycardia, or multifocal atrial tachycardia), infra-Hisian conduction system disease, and vulnerability to dilated cardiomyopathy. Age of onset ranges between childhood and adulthood.
Id1197418004
StatusPrimitive
Finding sitestructuur van geleidingssysteem van hart
Has interpretationverhoogd
Interpretshartslagfrequentie
Finding sitestructuur van atrium cordis
SNOMED CT to Orphanet simple map436242
SNOMED CT to ICD-10 extended map
TargetI45.8
RuleTRUE
AdviceALWAYS I45.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified