familial mitral valve prolapse
MONDO:0008004Mondo
Findings
No curated finding names familial mitral valve prolapse yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
An instance of mitral valve prolapse (disease) that is caused by an inherited modification of the individual's genome.
Definition from the Mondo Disease Ontology (MONDO:0008004), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- DCHS1HGNC:13681
- Supportive · Orphanet · Autosomal dominant · 2021
Where it sits
Other names
1 name
Resolves to: familial mitral valve prolapse
- Also called
- hereditary mitral valve prolapse (disease)