Abnormality of the mitral valve
Symptom Information:
Symptom ID: | HPO:0001633 | ||
Synonyms: |
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Quality: | |||
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) MedDRA: |
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Database Frequency: | 69 / 7739 | ||
Resource: |
All diseases associated with this symptom:
16q24.3 microdeletion syndrome | (Orphanet:261250) |
19p13.12 microdeletion syndrome | (Orphanet:254346) |
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
3C syndrome | (Orphanet:7) |
8p11.2 deletion syndrome | (Orphanet:251066) |
Acro-cardio-facial syndrome | (Orphanet:2008) |
Acromegaly | (Orphanet:963) |
Acroosteolysis, dominant type | (Orphanet:955) |
Alkaptonuria | (Orphanet:56) |
Anophthalmia - megalocornea - cardiopathy - skeletal anomalies | (Orphanet:1101) |
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy | (Orphanet:1192) |
Behçet disease | (Orphanet:117) |
Brachydactyly - mesomelia - intellectual deficit - heart defects | (Orphanet:1277) |
Brachymorphism - onychodysplasia - dysphalangism | (Orphanet:1292) |
Brittle cornea syndrome | (Orphanet:90354) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cardiomyopathy, familial hypertrophic, 14 | (OMIM:613251) |
Cardiospondylocarpofacial syndrome | (Orphanet:3238) |
Chronic atrial and intestinal dysrhythmia syndrome | (Orphanet:435988) |
Coffin-Lowry syndrome | (Orphanet:192) |
Cogan syndrome | (Orphanet:1467) |
Cohen syndrome | (Orphanet:193) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Costello syndrome | (Orphanet:3071) |
Criss-cross heart | (Orphanet:1461) |
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, classic type | (Orphanet:287) |
Ehlers-Danlos syndrome, kyphoscoliotic type | (Orphanet:1900) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
FACES syndrome | (Orphanet:1969) |
Fabry disease | (Orphanet:324) |
Familial isolated hypertrophic cardiomyopathy | (Orphanet:155) |
Fragile X syndrome | (Orphanet:908) |
Gaucher disease | (Orphanet:355) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Geleophysic dysplasia | (Orphanet:2623) |
Heart defects - limb shortening | (Orphanet:1354) |
Hurler syndrome | (Orphanet:93473) |
Hydrocephaly - tall stature - joint laxity | (Orphanet:2181) |
Hypogonadism - mitral valve prolapse - intellectual deficit | (Orphanet:2233) |
Hypoplastic left heart syndrome | (Orphanet:2248) |
Hypospadias - hypertelorism - coloboma and deafness | (Orphanet:157788) |
LEOPARD SYNDROME 3 | (OMIM:613707) |
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus | (Orphanet:83473) |
Microphthalmia with linear skin defects syndrome | (Orphanet:2556) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Oculogastrointestinal muscular dystrophy | (Orphanet:1876) |
Polymyositis | (Orphanet:732) |
Polyvalvular heart disease syndrome | (Orphanet:228410) |
Pseudoxanthoma elasticum | (Orphanet:758) |
Relapsing polychondritis | (Orphanet:728) |
Rheumatic fever | (Orphanet:3099) |
Short stature - valvular heart disease - characteristic facies | (Orphanet:2868) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Sneddon syndrome | (Orphanet:820) |
Stickler syndrome | (Orphanet:828) |
Stickler syndrome type 1 | (Orphanet:90653) |
Syndactyly - telecanthus - anogenital and renal malformations | (Orphanet:140952) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Von Willebrand disease | (Orphanet:903) |
Weill-Marchesani syndrome | (Orphanet:3449) |
Williams syndrome | (Orphanet:904) |
X-linked mandibulofacial dysostosis | (Orphanet:1131) |