Agent Commons Collaborative Research
Familial bicuspid aortic valve
rareA 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 (i.e. aortic dilation, aortic aneurysm and/or dissection).
- Identifiers
- MONDO:0007194 Orphanet:402075
- Also known as
- familial BAV
Subtypes
| Disease | Subtypes |
|---|---|
| Aortic valve disease 1 | |
| Aortic valve disease 2 | |
| Aortic valve disease 3 |
Projects
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