Aortic dilatation

Symptom Information:

Symptom ID: HPO:0001724
Synonyms:
Aortic aneurysm [Orphanet:34660]
Aortic aneurysm (disorder) [Orphanet:34660]
Aortic aneurysm without mention of rupture NOS [Orphanet:34660]
Aortic Aneurysm [Orphanet:34660]
Aortic dilatation [OMIM:Aortic dilatation]
Aortic dilatation/dilation [Orphanet:34660]
Aortic aneurysm of unspecified site without mention of rupture [Orphanet:34660]
Aortic aneurysm [MedDRA:10002882]
Abdominal aneurysm [MedDRA:10002882]
Abdominal aneurysm without mention of rupture [MedDRA:10002882]
Abdominal aortic aneurysm [MedDRA:10002882]
Aneurysm aortic [MedDRA:10002882]
Aneurysm of abdominal aorta [MedDRA:10002882]
Aneurysm of aorta [MedDRA:10002882]
Aneurysm of aortic arch [MedDRA:10002882]
Aneurysm of arch of aorta [MedDRA:10002882]
Aneurysm of ascending aorta [MedDRA:10002882]
Aneurysm of descending aorta [MedDRA:10002882]
Aortic aneurysm of unspecified site without mention of rupture [MedDRA:10002882]
Thoracic aneurysm without mention of rupture [MedDRA:10002882]
Thoracic aortic aneurysm [MedDRA:10002882]
Thoracoabdominal aneurysm, without mention of rupture [MedDRA:10002882]
Thoracoabdominal aortic aneurysm [MedDRA:10002882]
Aortic aneurysm enlargement [MedDRA:10002882]
Ascending aortic aneurysm enlargement [MedDRA:10002882]
Descending thoracic aortic aneurysm enlargement [MedDRA:10002882]
Abdominal aortic aneurysm enlargement [MedDRA:10002882]
Abdominal aortic aneurysm (in some patients) [OMIM:Abdominal aortic aneurysm (in some patients)]
Aortic aneurysms (ascending or aortic arch) [OMIM:Aortic aneurysms (ascending or aortic arch)]
Aortic dilatation (1 family) [OMIM:Aortic dilatation (1 family)]
Aortic dilatation (reported in 1 patient) [OMIM:Aortic dilatation (reported in 1 patient)]
Thoracic aortic aneurysm [OMIM:Thoracic aortic aneurysm]
Aortic dilatation [MedDRA:10057453]
Quality:
Cross references:
HPO:0004942 "Aortic aneurysm" [Orphanet:34660]
Orphanet:34660 "Aortic dilatation/dilation" [Orphanet:34660]
OMIM: "Aortic dilatation" [OMIM:Aortic dilatation]
OMIM: "Abdominal aortic aneurysm (in some patients)" [OMIM:Abdominal aortic aneurysm (in some patients)]
OMIM: "Aortic aneurysms (ascending or aortic arch)" [OMIM:Aortic aneurysms (ascending or aortic arch)]
OMIM: "Aortic dilatation (1 family)" [OMIM:Aortic dilatation (1 family)]
OMIM: "Aortic dilatation (reported in 1 patient)" [OMIM:Aortic dilatation (reported in 1 patient)]
OMIM: "Thoracic aortic aneurysm" [OMIM:Thoracic aortic aneurysm]
UMLS:C0340629 "Aortic aneurysm without mention of rupture NOS" [Orphanet:34660]
UMLS:C0003486 "Aortic Aneurysm" [Orphanet:34660]
Is a (Direct Parents):
MedDRA Aortic aneurysms and dissections
MedDRA Site specific vascular disorders NEC
HPO         Abnormality of the aorta
Orphanet Structural anomalies of the cardio-circulatory system
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)