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familiaire gedilateerde cardiomyopathie met geleidingsdefect door mutatie in LMNA-gen (aandoening)
familiaire gedilateerde cardiomyopathie met geleidingsdefect door mutatie in LMNA-gen
familiaire gedilateerde cardiomyopathie met geleidingsdefect door LMNA-mutatie
familiaire gedilateerde cardiomyopathie met geleidingsdefect door mutatie van lamin A/C
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation
A rare familial dilated cardiomyopathy with characteristics of left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy and elevated serum creatine kinase.
Id766883006
StatusPrimitive
Associated morphologydilatatie
Finding sitestructuur van myocardium
referentieset met complexe 'mapping' naar ICD-10
TargetI42.0
RuleTRUE
AdviceALWAYS I42.0 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified