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syndroom van atriumseptumdefect en atrioventriculair geleidingsdefect (aandoening)
syndroom van atriumseptumdefect en atrioventriculair geleidingsdefect
Atrial septal defect, atrioventricular conduction defect syndrome
An extremely rare genetic congenital heart disease with the presence of atrial septal defect, mostly of the ostium secundum type, associated with conduction anomalies like atrioventricular block, atrial fibrillation or right bundle branch block. There is evidence this disease is caused by heterozygous mutation in the NKX2-5 gene on chromosome 5q35.
Id725145002
StatusPrimitive
Associated morphologydefect
Finding sitestructuur van septum interatriale
Occurrencecongenitaal
Pathological processproces van pathologische ontwikkeling
referentieset met complexe 'mapping' naar ICD-10
TargetQ21.1
RuleTRUE
AdviceALWAYS Q21.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified