Mitral regurgitation
Symptom Information:
Symptom ID: | HPO:0001653 | ||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |