has characteristic has characteristic mitral valve prolapse familial mitral valve prolapse https://www.malacards.org/card/mitral_valve_prolapse_1 OMIMPS:157700 MONDO:0008004 MVP GARD:0003687 SCTID:233858000 An instance of mitral valve prolapse (disease) that is caused by an inherited modification of the individual's genome. hereditary mitral valve prolapse (disease) Orphanet:741 UMLS:C0340364 mitral valve prolapse, familial mitral valve prolapse, familial, autosomal dominant MEDGEN:573696 congenital mitral valve insufficiency and/or stenosis inherited inherited mitral valve disease