| 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. |
| | Id | 725145002 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q21.1 | | Term | Atriumseptumdefect |
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| SNOMED CT to Orphanet simple map | 1479 |
| SNOMED CT to ICD-10 extended map | | Target | Q21.1 | | Rule | TRUE | | Advice | ALWAYS Q21.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION | | Correlation | SNOMED CT source code to target map code correlation not specified |
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