Mitral valve prolapse 3

Preferred Label : Mitral valve prolapse 3;

Symbol : MVP3;

CISMeF acronym : MMVP3; MVP3;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Mitral valve prolapse, myxomatous 3; Myxomatous mitral valve prolapse 3; MMVP3;

Description : Mitral valve prolapse (MVP) is a common disorder characterized by histologic displacement or billowing of the mitral leaflets into the left atrium, often accompanied by mitral regurgitation. For a general phenotypic description and a discussion of genetic heterogeneity of mitral valve prolapse, see MMVP1 (157700).;

Inheritance : Autosomal dominant;

Prefixed ID : #610840;

Détails

Origin ID

610840;

UMLS CUI

C1835814;

Currated CISMeF NLP mapping
- mitral valve prolapse, myxomatous 3 [MeSH concept]
- mitral valve prolapse, myxomatous 3 [MeSH Supplementary Concept]
DO Cross reference
- mitral valve prolapse [DO Concept]
Genes related to phenotype
- Daz-interacting zinc finger protein 1 [OMIM gene]
HPO term(s)
- Age-dependent penetrance [HPO term]
- Autosomal dominant inheritance [HPO term]
- Mitral regurgitation [HPO term]
- Mitral valve prolapse [HPO term]
ORDO concept(s)
- Familial mitral valve prolapse [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- mitral valve prolapse, myxomatous 3 [MeSH Supplementary Concept]
- mitral valve prolapse, myxomatous 3 [MeSH concept]

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