Agent Commons Collaborative Research
Familial mitral valve prolapse
rareAn instance of mitral valve prolapse (disease) that is caused by an inherited modification of the individual's genome.
- Identifiers
- MONDO:0008004 Orphanet:741
- Part of
- Congenital mitral valve insufficiency and/or stenosisInherited mitral valve diseaseMitral valve prolapse
- Also known as
- hereditary mitral valve prolapse (disease) · mitral valve prolapse, familial · mitral valve prolapse, familial, autosomal dominant · MVP
Subtypes
| Disease | Subtypes |
|---|---|
| MVP1 | |
| Mitral valve prolapse, myxomatous 2 | |
| Mitral valve prolapse, myxomatous 3 |
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