Mitral valve prolapse
Symptom Information:
Symptom ID: | HPO:0001634 | |||||||||||||||
Synonyms: |
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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 valve prolapse(HPO:0001634) MedDRA: Cardiac disorders(MedDRA:10007541) Cardiac valve disorders(MedDRA:10046973) Mitral valvular disorders(MedDRA:10027723) Mitral valve prolapse(HPO:0001634) |
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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) |