C4510872_SNOMEDCT_US | Knowledge4COVID-19

Property	Value
?:definition	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.
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?:type	<https://research.tib.eu/covid-19/vocab/AnnotationDefinition>

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