Aortic valve stenosis
Symptom Information:
Symptom ID: | HPO:0001650 | |||||||||||||||||||
Synonyms: |
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Cross references: |
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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 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) |
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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) |