Ascending aortic aneurysm
Symptom Information:
Symptom ID: | HPO:0002631 | ||||
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) Abnormality of the vasculature(HPO:0002597) Abnormality of the systemic arterial tree(HPO:0011004) Abnormality of the aorta(HPO:0001679) Aortic dilatation(HPO:0001724) Dilatation of the ascending aorta(HPO:0005111) Ascending aortic aneurysm(HPO:0002631) Aortic aneurysm(HPO:0004942) Ascending aortic aneurysm(HPO:0002631) Aneurysm(HPO:0002617) Aortic aneurysm(HPO:0004942) Ascending aortic aneurysm(HPO:0002631) MedDRA: |
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Database Frequency: | 9 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA | (OMIM:219100) |
LOEYS-DIETZ SYNDROME 1 | (OMIM:609192) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
LOEYS-DIETZ SYNDROME, TYPE 2A | (OMIM:608967) |
LUJAN-FRYNS SYNDROME | (OMIM:309520) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
Marfan syndrome type 1 | (Orphanet:284963) |
Marfan syndrome type 2 | (Orphanet:284973) |