MeSH Browser

MeSH Supplementary: Barlow syndrome
Unique ID: C537478
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537478
Entry Term(s): Mitral regurgitation, familial; Mitral valve prolapse, familial, X-linked; Myxomatous valvular disease, familial
Registry Numbers: 0
Heading Mapped to: *Mitral Valve Prolapse
Frequency: 66
Note: A genetically heterogeneous hereditary form of mitral valve prolapse that appears to be inherited as an autosomal dominant or x-linked trait and exhibits both sex- and age-dependent PENETRANCE. OMIM: 157700
Date of Entry: 2010/08/25
Revision Date: 2017/10/19

Barlow syndrome MeSH Supplementary Concept Data 2025