Aortic valve stenosis

Symptom Information:

Symptom ID: HPO:0001650
Synonyms:
Aortic stenosis [HPO:0001650]
Valvular aortic stenosis [HPO:0001650]
Aortic valve stenosis (disorder) [Orphanet:34140]
Aortic Valve Stenosis [Orphanet:34140]
Aortic stenosis [OMIM:Aortic stenosis]
Aortic valve stenosis [OMIM:Aortic valve stenosis]
Valvular aortic stenosis [OMIM:Valvular aortic stenosis]
Aortic valve atresia/stenosis/narrowing/supra-aortic/supra-valvular stenosis [Orphanet:34140]
Aortic valve stenosis [Orphanet:34140]
Aortic stenosis [Orphanet:34140]
Aortic valve stenosis [MedDRA:10002918]
Rheumatic aortic stenosis [MedDRA:10002918]
Stenosis aortic valve [MedDRA:10002918]
Aortic stenosis [MedDRA:10002906]
Aortic stricture [MedDRA:10002906]
Aorto-iliac arterial stenosis [MedDRA:10002906]
Abdominal aortic stenosis [MedDRA:10002906]
Aortic stenosis (in some patients) [OMIM:Aortic stenosis (in some patients)]
Aortic stenosis (variable) [OMIM:Aortic stenosis (variable)]
Quality:
Cross references:
Orphanet:34140 "Aortic valve atresia/stenosis/narrowing/supra-aortic/supra-valvular stenosis" [Orphanet:34140]
OMIM: "Aortic stenosis" [OMIM:Aortic stenosis]
OMIM: "Aortic valve stenosis" [OMIM:Aortic valve stenosis]
OMIM: "Valvular aortic stenosis" [OMIM:Valvular aortic stenosis]
OMIM: "Aortic stenosis (in some patients)" [OMIM:Aortic stenosis (in some patients)]
OMIM: "Aortic stenosis (variable)" [OMIM:Aortic stenosis (variable)]
UMLS:C0003507 "Aortic Valve Stenosis" [Orphanet:34140]
Is a (Direct Parents):
HPO         Abnormality of the aortic valve
MedDRA Aortic necrosis and vascular insufficiency
Orphanet Abnormality of the heart valves
MedDRA Aortic valvular disorders
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 valve stenosis(HPO:0001650)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216)
       Aortic necrosis and vascular insufficiency(MedDRA:10002901)
          Aortic valve stenosis(HPO:0001650)
Cardiac disorders(MedDRA:10007541)
    Cardiac valve disorders(MedDRA:10046973)
       Aortic valvular disorders(MedDRA:10002911)
          Aortic valve stenosis(HPO:0001650)
Database Frequency: 49 / 7739
Resource:

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
AORTIC VALVE DISEASE 1 (OMIM:109730)
Arterial tortuosity syndrome (Orphanet:3342)
Autosomal recessive infantile hypercalcemia (Orphanet:300547)
BARAITSER-WINTER SYNDROME 1 (OMIM:243310)
Baraitser-Winter syndrome (Orphanet:2995)
CALCIFIC AORTIC DISEASE WITH IMMUNOLOGIC ABNORMALITIES, FAMILIAL (OMIM:114065)
CHST3-related skeletal dysplasia (Orphanet:263463)
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 4 (OMIM:615779)
Dandy-Walker malformation - postaxial polydactyly (Orphanet:1566)
Emanuel syndrome (Orphanet:96170)
GELEOPHYSIC DYSPLASIA 1 (OMIM:231050)
GELEOPHYSIC DYSPLASIA 2 (OMIM:614185)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Geleophysic dysplasia (Orphanet:2623)
Glaucoma - ectopia - microspherophakia - stiff joints - short stature (Orphanet:2084)
Hurler-Scheie syndrome (Orphanet:93476)
Hypoplastic left heart syndrome 1 (OMIM:241550)
Joubert syndrome 28 (OMIM:617121)
LMNA-related cardiocutaneous progeria syndrome (Orphanet:363618)
Lymphoid interstitial pneumonia (Orphanet:79128)
MUCOLIPIDOSIS III GAMMA (OMIM:252605)
McDonough syndrome (Orphanet:2471)
Monosomy 18q (Orphanet:1600)
Mowat-Wilson syndrome (Orphanet:2152)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Myhre syndrome (Orphanet:2588)
Nephronophthisis 16 (OMIM:615382)
Nephronophthisis 9 (OMIM:613824)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Oculofaciocardiodental syndrome (Orphanet:2712)
PSYCHOMOTOR RETARDATION, EPILEPSY, AND CRANIOFACIAL DYSMORPHISM (OMIM:614501)
Pfeiffer-Palm-Teller syndrome (Orphanet:2871)
Progeria - short stature - pigmented nevi (Orphanet:2959)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
Renal-hepatic-pancreatic dysplasia (Orphanet:294415)
SC PHOCOMELIA SYNDROME (OMIM:269000)
SINGLETON-MERTEN SYNDROME 2 (OMIM:616298)
STORM SYNDROME (OMIM:185069)
Scheie syndrome (Orphanet:93474)
Singleton-Merten dysplasia (Orphanet:85191)
Tetrasomy 12p (Orphanet:884)
Von Willebrand disease type 1 (Orphanet:166078)
WEILL-MARCHESANI SYNDROME 1 (OMIM:277600)
WEILL-MARCHESANI SYNDROME 3 (OMIM:614819)
Weill-Marchesani syndrome (Orphanet:3449)
Williams syndrome (Orphanet:904)
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome (Orphanet:324410)