Mitral regurgitation

Symptom Information:

Symptom ID: HPO:0001653
Synonyms:
Mitral incompetence [HPO:0001653]
Mitral insufficiency [HPO:0001653]
MITRAL REGURGITATION, MILD [HPO:0001653]
Mitral valve insufficiency [HPO:0001653]
Mitral valve regurgitation [HPO:0001653]
Mitral valve insufficiency [Orphanet:34040]
Mitral valve regurgitation (disorder) [Orphanet:34040]
Mitral Valve Insufficiency [Orphanet:34040]
Mitral insufficiency [OMIM:Mitral insufficiency]
Mitral regurgitation [OMIM:Mitral regurgitation]
Mitral regurgitation, mild [OMIM:Mitral regurgitation, mild]
Mitral valve insufficiency [OMIM:Mitral valve insufficiency]
Mitral valve regurgitation [OMIM:Mitral valve regurgitation]
Mitral valve prolapse/incompetence/insufficiency/regurgitation/ring anomaly [Orphanet:34040]
Mitral valve incompetence [Orphanet:34040]
Mitral valve incompetence [MedDRA:10027727]
Mitral incompetence [MedDRA:10027727]
Mitral insufficiency [MedDRA:10027727]
Mitral regurgitation [MedDRA:10027727]
Rheumatic mitral incompetence [MedDRA:10027727]
Rheumatic mitral insufficiency [MedDRA:10027727]
Mitral valve incompetence aggr. [MedDRA:10027727]
Mitral regurgitation (in some patients) [OMIM:Mitral regurgitation (in some patients)]
Mitral valve insufficiency (in some patients) [OMIM:Mitral valve insufficiency (in some patients)]
Mitral valve regurgitation (1 family) [OMIM:Mitral valve regurgitation (1 family)]
Intramitral mitral ring [Orphanet:34040]
Quality:
Cross references:
Orphanet:34040 "Mitral valve prolapse/incompetence/insufficiency/regurgitation/ring anomaly" [Orphanet:34040]
OMIM: "Mitral insufficiency" [OMIM:Mitral insufficiency]
OMIM: "Mitral regurgitation" [OMIM:Mitral regurgitation]
OMIM: "Mitral regurgitation, mild" [OMIM:Mitral regurgitation, mild]
OMIM: "Mitral valve insufficiency" [OMIM:Mitral valve insufficiency]
OMIM: "Mitral valve regurgitation" [OMIM:Mitral valve regurgitation]
OMIM: "Mitral regurgitation (in some patients)" [OMIM:Mitral regurgitation (in some patients)]
OMIM: "Mitral valve insufficiency (in some patients)" [OMIM:Mitral valve insufficiency (in some patients)]
OMIM: "Mitral valve regurgitation (1 family)" [OMIM:Mitral valve regurgitation (1 family)]
UMLS:C0026266 "Mitral Valve Insufficiency" [Orphanet:34040]
Is a (Direct Parents):
Orphanet Mitral valve prolapse
Orphanet Abnormality of the heart valves
MedDRA Mitral valvular disorders
HPO         Abnormality of the mitral valve
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 regurgitation(HPO:0001653)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Cardiac valve disorders(MedDRA:10046973)
       Mitral valvular disorders(MedDRA:10027723)
          Mitral regurgitation(HPO:0001653)
Database Frequency: 64 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Aspartylglucosaminuria (Orphanet:93)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Atrial fibrillation, familial, 10 (OMIM:614022)
Atrial standstill (Orphanet:1344)
Autosomal dominant cutis laxa (Orphanet:90348)
Autosomal recessive progressive external ophthalmoplegia (Orphanet:254886)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
CHST3-related skeletal dysplasia (Orphanet:263463)
CUTIS LAXA, AUTOSOMAL DOMINANT 1 (OMIM:123700)
CUTIS LAXA, AUTOSOMAL DOMINANT 2 (OMIM:614434)
Cardiomyopathy, dilated, 1II (OMIM:615184)
Cardiomyopathy, dilated, 1KK (OMIM:615248)
Cardiospondylocarpofacial syndrome (Orphanet:3238)
Carney complex (Orphanet:1359)
Chronic atrial and intestinal dysrhythmia syndrome (Orphanet:435988)
Coffin-Lowry syndrome (Orphanet:192)
Congenital contractural arachnodactyly (Orphanet:115)
Congenital heart block (Orphanet:60041)
Congenital valvular dysplasia (Orphanet:1864)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Deafness - encephaloneuropathy - obesity - valvulopathy (Orphanet:254898)
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome (Orphanet:2229)
ENDOCARDIAL FIBROELASTOSIS AND COARCTATION OF ABDOMINAL AORTA (OMIM:226100)
Ehlers-Danlos syndrome, cardiac valvular type (Orphanet:230851)
Fabry disease (Orphanet:324)
Familial isolated hypertrophic cardiomyopathy (Orphanet:155)
GELEOPHYSIC DYSPLASIA 2 (OMIM:614185)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
His bundle tachycardia (Orphanet:3283)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypoplastic left heart syndrome (Orphanet:2248)
Hypoplastic left heart syndrome 1 (OMIM:241550)
Hypoplastic left heart syndrome 2 (OMIM:614435)
Incessant infant ventricular tachycardia (Orphanet:45453)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (OMIM:175050)
LMNA-related cardiocutaneous progeria syndrome (Orphanet:363618)
Left ventricular noncompaction 1 (OMIM:604169)
Left ventricular noncompaction 8 (OMIM:615373)
Loeffler endocarditis (Orphanet:75566)
MARFANOID HYPERMOBILITY SYNDROME (OMIM:154750)
MITRAL VALVE PROLAPSE, MYXOMATOUS 2 (OMIM:607829)
MITRAL VALVE PROLAPSE, MYXOMATOUS 3 (OMIM:610840)
Marfan syndrome type 1 (Orphanet:284963)
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus (Orphanet:83473)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Nephronophthisis 2 (OMIM:602088)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Polyvalvular heart disease syndrome (Orphanet:228410)
Pseudoxanthoma elasticum (Orphanet:758)
RIENHOFF SYNDROME (OMIM:615582)
Spondyloepimetaphyseal dysplasia with joint laxity (Orphanet:93359)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
Weill-Marchesani syndrome (Orphanet:3449)
Williams syndrome (Orphanet:904)