Aortic regurgitation

Symptom Information:

Symptom ID: HPO:0001659
Synonyms:
Aortic insufficiency [HPO:0001659]
Aortic valve regurgitation [HPO:0001659]
Aortic valve insufficiency [Orphanet:34120]
Aortic valve regurgitation (disorder) [Orphanet:34120]
Aortic Valve Insufficiency [Orphanet:34120]
Aortic insufficiency [OMIM:Aortic insufficiency]
Aortic regurgitation [OMIM:Aortic regurgitation]
Aortic valve regurgitation [OMIM:Aortic valve regurgitation]
Aortic valve anomaly/incompetence/insufficiency/regurgitation/bicuspid [Orphanet:34120]
Aortic valve incompetence [Orphanet:34120]
Aortic valve incompetence [MedDRA:10002915]
Aortic incompetence [MedDRA:10002915]
Aortic regurgitation [MedDRA:10002915]
Rheumatic aortic incompetence [MedDRA:10002915]
Rheumatic aortic insufficiency [MedDRA:10002915]
Aortic valve insufficiency [MedDRA:10002915]
Aortic insufficiency (in some patients) [OMIM:Aortic insufficiency (in some patients)]
Aortic regurgitation (in some patients) [OMIM:Aortic regurgitation (in some patients)]
Aortic valve insufficiency [OMIM:Aortic valve insufficiency]
Quality:
Cross references:
Orphanet:34120 "Aortic valve anomaly/incompetence/insufficiency/regurgitation/bicuspid" [Orphanet:34120]
OMIM: "Aortic insufficiency" [OMIM:Aortic insufficiency]
OMIM: "Aortic regurgitation" [OMIM:Aortic regurgitation]
OMIM: "Aortic valve regurgitation" [OMIM:Aortic valve regurgitation]
OMIM: "Aortic insufficiency (in some patients)" [OMIM:Aortic insufficiency (in some patients)]
OMIM: "Aortic regurgitation (in some patients)" [OMIM:Aortic regurgitation (in some patients)]
OMIM: "Aortic valve insufficiency" [OMIM:Aortic valve insufficiency]
UMLS:C0003504 "Aortic Valve Insufficiency" [Orphanet:34120]
Is a (Direct Parents):
Orphanet Abnormality of the heart valves
HPO         Abnormality of the aortic valve
MedDRA Aortic valvular disorders
Orphanet Abnormality of the aortic valve
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 heart valves(HPO:0001654)
                   Abnormality of the aortic valve(HPO:0001646)
                      Aortic regurgitation(HPO:0001659)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Cardiac valve disorders(MedDRA:10046973)
       Aortic valvular disorders(MedDRA:10002911)
          Aortic regurgitation(HPO:0001659)
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

AORTIC ANEURYSM, FAMILIAL THORACIC 4 (OMIM:132900)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Arterial tortuosity syndrome (Orphanet:3342)
Autosomal dominant cutis laxa (Orphanet:90348)
CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL (OMIM:114065)
CHST3-related skeletal dysplasia (Orphanet:263463)
CUTIS LAXA, AUTOSOMAL DOMINANT 1 (OMIM:123700)
Chronic atrial and intestinal dysrhythmia syndrome (Orphanet:435988)
Congenital valvular dysplasia (Orphanet:1864)
D-2-@HYDROXYGLUTARIC ACIDURIA 1 (OMIM:600721)
D-2-hydroxyglutaric aciduria (Orphanet:79315)
Deafness - encephaloneuropathy - obesity - valvulopathy (Orphanet:254898)
Ehlers-Danlos syndrome, cardiac valvular type (Orphanet:230851)
Fabry disease (Orphanet:324)
GELEOPHYSIC DYSPLASIA 2 (OMIM:614185)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
HUNTER-MACDONALD SYNDROME (OMIM:611962)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
MARFANOID HABITUS WITH SITUS INVERSUS (OMIM:609008)
MARFANOID HYPERMOBILITY SYNDROME (OMIM:154750)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 (OMIM:614114)
MUCOLIPIDOSIS III ALPHA/BETA (OMIM:252600)
MUCOLIPIDOSIS III GAMMA (OMIM:252605)
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY (OMIM:601347)
Marfan syndrome type 1 (Orphanet:284963)
Mucolipidosis type 2 (Orphanet:576)
Mucolipidosis type 3 (Orphanet:577)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Nephronophthisis 15 (OMIM:614845)
SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1 (OMIM:106300)
Scheie syndrome (Orphanet:93474)
Syndromic diarrhea (Orphanet:84064)
TRICHOHEPATOENTERIC SYNDROME 1 (OMIM:222470)
Temtamy syndrome (Orphanet:1777)