Abnormality of the mitral valve

Symptom Information:

Symptom ID: HPO:0001633
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the atrioventricular valves
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:
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)
Beh├žet 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)