Aortic dilatation
Symptom Information:
Symptom ID: | HPO:0001724 | |||||||||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of the vasculature(HPO:0002597) Abnormality of the systemic arterial tree(HPO:0011004) Abnormality of the aorta(HPO:0001679) Aortic dilatation(HPO:0001724) MedDRA: Vascular disorders(MedDRA:10047065) Vascular disorders NEC(MedDRA:10047066) Site specific vascular disorders NEC(MedDRA:10057188) Aortic dilatation(HPO:0001724) Aneurysms and artery dissections(MedDRA:10002363) Aortic aneurysms and dissections(MedDRA:10002889) Aortic dilatation(HPO:0001724) |
|||||||||||||||||||||||||||||||||
Database Frequency: | 24 / 7739 | |||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AORTIC ANEURYSM, FAMILIAL THORACIC 4 | (OMIM:132900) |
AORTIC ANEURYSM, FAMILIAL THORACIC 6 | (OMIM:611788) |
AORTIC ANEURYSM, FAMILIAL THORACIC 7 | (OMIM:613780) |
AORTIC ANEURYSM, FAMILIAL THORACIC 8 | (OMIM:615436) |
Alkaptonuria | (Orphanet:56) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2 | (OMIM:614980) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IB | (OMIM:614437) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Costello syndrome | (Orphanet:3071) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
Hereditary arterial and articular multiple calcification syndrome | (Orphanet:289601) |
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME | (OMIM:175050) |
Koolen-De Vries syndrome | (Orphanet:96169) |
MASS SYNDROME | (OMIM:604308) |
MELAS | (Orphanet:550) |
MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME | (OMIM:613834) |
Osteogenesis imperfecta type 1 | (Orphanet:216796) |
PHACE syndrome | (Orphanet:42775) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Temtamy syndrome | (Orphanet:1777) |