Mitral valve prolapse

Symptom Information:

Symptom ID: HPO:0001634
Synonyms:
Mitral valve prolapse (disorder) [Orphanet:34040]
Mitral Valve Prolapse Syndrome [Orphanet:34040]
Mitral valve prolapse [OMIM:Mitral valve prolapse]
Mitral valve prolapse/incompetence/insufficiency/regurgitation/ring anomaly [Orphanet:34040]
Mitral valve prolapse [Orphanet:34040]
Mitral valve prolapse [MedDRA:10027730]
Barlow's syndrome [MedDRA:10027730]
Floppy mitral valve [MedDRA:10027730]
Mitral leaflet prolapse [MedDRA:10027730]
Prolapsed mitral valve [MedDRA:10027730]
Mitral valve prolapse (1 family) [OMIM:Mitral valve prolapse (1 family)]
Mitral valve prolapse (rare) [OMIM:Mitral valve prolapse (rare)]
Mitral valve prolapse (seen in patients with contiguous gene defect) [OMIM:Mitral valve prolapse (seen in patients with contiguous gene defect)]
Mitral valve prolapse (uncommon) [OMIM:Mitral valve prolapse (uncommon)]
Intramitral mitral ring [Orphanet:34040]
Quality:
Cross references:
Orphanet:34040 "Mitral valve prolapse/incompetence/insufficiency/regurgitation/ring anomaly" [Orphanet:34040]
OMIM: "Mitral valve prolapse" [OMIM:Mitral valve prolapse]
OMIM: "Mitral valve prolapse (1 family)" [OMIM:Mitral valve prolapse (1 family)]
OMIM: "Mitral valve prolapse (rare)" [OMIM:Mitral valve prolapse (rare)]
OMIM: "Mitral valve prolapse (seen in patients with contiguous gene defect)" [OMIM:Mitral valve prolapse (seen in patients with contiguous gene defect)]
OMIM: "Mitral valve prolapse (uncommon)" [OMIM:Mitral valve prolapse (uncommon)]
UMLS:C0026267 "Mitral Valve Prolapse Syndrome" [Orphanet:34040]
Is a (Direct Parents):
HPO         Abnormality of the mitral valve
Orphanet Abnormality of the heart valves
MedDRA Mitral valvular disorders
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormal heart morphology(HPO:0001627)
             obsolete Malformation of the heart and great vessels(HPO:0002564)
                Abnormality of the atrioventricular valves(HPO:0006705)
                   Abnormality of the mitral valve(HPO:0001633)
                      Mitral valve prolapse(HPO:0001634)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Cardiac valve disorders(MedDRA:10046973)
       Mitral valvular disorders(MedDRA:10027723)
          Mitral valve prolapse(HPO:0001634)
Database Frequency: 69 / 7739
Resource:

All diseases associated with this symptom:

AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM (OMIM:104350)
AORTIC ANEURYSM, FAMILIAL THORACIC 9 (OMIM:616166)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Autosomal recessive progressive external ophthalmoplegia (Orphanet:254886)
BRITTLE CORNEA SYNDROME 1 (OMIM:229200)
Brittle cornea syndrome (Orphanet:90354)
CARDIOFACIOCUTANEOUS SYNDROME 2 (OMIM:615278)
Cardiomyopathy, familial hypertrophic, 21 (OMIM:614676)
Carney complex (Orphanet:1359)
Classical homocystinuria (Orphanet:394)
Cohen syndrome (Orphanet:193)
Congenital contractural arachnodactyly (Orphanet:115)
Congenital valvular dysplasia (Orphanet:1864)
Costello syndrome (Orphanet:3071)
Dahlberg-Borer-Newcomer syndrome (Orphanet:1563)
Dermato-cardio-skeletal syndrome, Borrone type (Orphanet:1266)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome type 2 (Orphanet:90318)
Ehlers-Danlos syndrome, cardiac valvular type (Orphanet:230851)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, fibronectinemic type (Orphanet:75501)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Fabry disease (Orphanet:324)
Faisalabad histiocytosis (Orphanet:254707)
Familial mitral valve prolapse (Orphanet:741)
Fragile X syndrome (Orphanet:908)
Frontometaphyseal dysplasia (Orphanet:1826)
GELEOPHYSIC DYSPLASIA 2 (OMIM:614185)
H syndrome (Orphanet:168569)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
Hypertaurinuric cardiomyopathy (OMIM:145350)
Hypoplastic left heart syndrome (Orphanet:2248)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (OMIM:175050)
LOEYS-DIETZ SYNDROME 1 (OMIM:609192)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
LOEYS-DIETZ SYNDROME 4 (OMIM:614816)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Left ventricular noncompaction 2 (OMIM:609470)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
MARFANOID HABITUS WITH SITUS INVERSUS (OMIM:609008)
MASS SYNDROME (OMIM:604308)
MITRAL VALVE PROLAPSE, MYXOMATOUS 2 (OMIM:607829)
MITRAL VALVE PROLAPSE, MYXOMATOUS 3 (OMIM:610840)
Marfan syndrome type 1 (Orphanet:284963)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Noonan syndrome (Orphanet:648)
OSTEOGENESIS IMPERFECTA, TYPE I (OMIM:166200)
Oculofaciocardiodental syndrome (Orphanet:2712)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Osteogenesis imperfecta type 1 (Orphanet:216796)
PSEUDOXANTHOMA ELASTICUM, FORME FRUSTEPSEUDOXANTHOMA ELASTICUM, HETEROZYGOUS, INCLUDED (OMIM:177850)
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome (Orphanet:254723)
Polyvalvular heart disease syndrome (Orphanet:228410)
Pseudoxanthoma elasticum (Orphanet:758)
Rosaï-Dorfman disease (Orphanet:158014)
STICKLER SYNDROME, TYPE I (OMIM:108300)
STORM SYNDROME (OMIM:185069)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Spondylo-ocular syndrome (Orphanet:85194)
Steinert myotonic dystrophy (Orphanet:273)
Stickler syndrome (Orphanet:828)
Tel Hashomer camptodactyly syndrome (Orphanet:3292)
Von Willebrand disease type 1 (Orphanet:166078)
Williams syndrome (Orphanet:904)
[DEL] PSEUDOXANTHOMA ELASTICUM (OMIM:264800)