Abnormality of the heart valves

Symptom Information:

Symptom ID: HPO:0001654
Valvular abnormality [HPO:0001654]
Valvular heart disease [HPO:0001654]
Valvular heart disease [Orphanet:34020]
Heart valve disorder (disorder) [Orphanet:34020]
Congenital anomaly of heart valve (disorder) [Orphanet:34020]
Congenital anomaly of heart valve [Orphanet:34020]
Heart valve disease [Orphanet:34020]
Valvular heart disease [OMIM:Valvular heart disease]
Cardiac valvulopathy [Orphanet:34020]
Cardiac valve disease [Orphanet:34020]
Cardiac valve disease [MedDRA:10061406]
Heart valve disorders [MedDRA:10061406]
Valvular heart disease NOS [MedDRA:10061406]
Cardiac valvulopathy [MedDRA:10061406]
Combined valvular disease [MedDRA:10061406]
Valvular heart disease (aortic and mitral valves) [OMIM:Valvular heart disease (aortic and mitral valves)]
Valvular heart disease (in a subset of patients) [OMIM:Valvular heart disease (in a subset of patients)]
Cross references:
Orphanet:34020 "Cardiac valvulopathy" [Orphanet:34020]
OMIM: "Valvular heart disease" [OMIM:Valvular heart disease]
OMIM: "Valvular heart disease (aortic and mitral valves)" [OMIM:Valvular heart disease (aortic and mitral valves)]
OMIM: "Valvular heart disease (in a subset of patients)" [OMIM:Valvular heart disease (in a subset of patients)]
UMLS:C0265820 "Congenital anomaly of heart valve" [Orphanet:34020]
UMLS:C0018824 "Heart valve disease" [Orphanet:34020]
Is a (Direct Parents):
MedDRA Cardiac valve disorders NEC
Orphanet Structural anomalies of the cardio-circulatory system
HPO         obsolete Malformation of the heart and great vessels
Is a (Whole tree): HPO:
    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 heart valves(HPO:0001654)
Cardiac disorders(MedDRA:10007541)
    Cardiac valve disorders(MedDRA:10046973)
       Cardiac valve disorders NEC(MedDRA:10046971)
          Abnormality of the heart valves(HPO:0001654)
Database Frequency: 49 / 7739

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
3C syndrome (Orphanet:7)
Alkaptonuria (Orphanet:56)
Autosomal dominant cutis laxa (Orphanet:90348)
CHILD syndrome (Orphanet:139)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cardiomyopathy-cataract-hip spine disease (Orphanet:1345)
Chronic atrial and intestinal dysrhythmia syndrome (Orphanet:435988)
Cogan syndrome (Orphanet:1467)
Cutis laxa (Orphanet:209)
Cutis laxa-Marfanoid syndrome (Orphanet:171719)
Ehlers-Danlos syndrome type 1 (Orphanet:90309)
Ehlers-Danlos syndrome with periventricular heterotopia (Orphanet:82004)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Ellis Van Creveld syndrome (Orphanet:289)
Fabry disease (Orphanet:324)
GM1 gangliosidosis (Orphanet:354)
GM1 gangliosidosis type 1 (Orphanet:79255)
Gaucher disease (Orphanet:355)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Gaucher disease type 3 (Orphanet:77261)
Geleophysic dysplasia (Orphanet:2623)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Kawasaki disease (Orphanet:2331)
Mosaic trisomy 9 (Orphanet:99776)
Mucolipidosis type 2 (Orphanet:576)
Mucolipidosis type 3 (Orphanet:577)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mucopolysaccharidosis type 4 (Orphanet:582)
Mucopolysaccharidosis type 4A (Orphanet:309297)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
Nephronophthisis 12 (OMIM:613820)
Nephronophthisis 2 (OMIM:602088)
Nephronophthisis 3 (OMIM:604387)
Pallister-Hall syndrome (Orphanet:672)
Rheumatic fever (Orphanet:3099)
Scheie syndrome (Orphanet:93474)
Short stature - valvular heart disease - characteristic facies (Orphanet:2868)
Sneddon syndrome (Orphanet:820)
Takayasu arteritis (Orphanet:3287)
Wolf-Hirschhorn syndrome (Orphanet:280)