Aortic regurgitation
Symptom Information:
Symptom ID: | HPO:0001659 | |||||||||||||||||||
Synonyms: |
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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 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) |
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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) |