| familiaire bicuspide aortaklep (aandoening) | | familiaire bicuspide aortaklep | | familiaire BAV
| | Familial bicuspid aortic valve | | Familial BAV (bicuspid aortic valve)
| | A rare genetic aortic malformation defined as a presence of abnormal two-leaflet aortic valve in at least 2 first-degree relatives. It is frequently asymptomatic or may be associated with progressive aortic valve disease (aortic regurgitation and/or aortic stenosis, typically due to valve calcification) and a concomitant aortopathy (such as aortic dilation, aortic aneurysm and/or dissection). |
| | Id | 770435005 | | Status | Primitive |
| DHD Diagnosis thesaurus reference set |
| RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set | | Target | Q23.1 | | Term | Congenitale insufficiëntie van aortaklep |
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| SNOMED CT to Orphanet simple map | 402075 |
| SNOMED CT to ICD-10 extended map | | Target | Q23.1 | | Rule | TRUE | | Advice | ALWAYS Q23.1 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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