Aortic root dilatation
Symptom Information:
Symptom ID: | HPO:0002616 | ||||||||
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) Dilatation of the ascending aorta(HPO:0005111) Aortic root dilatation(HPO:0002616) MedDRA: |
||||||||
Database Frequency: | 27 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Arterial tortuosity syndrome | (Orphanet:3342) |
Autosomal recessive cutis laxa type 1 | (Orphanet:90349) |
Blau syndrome | (Orphanet:90340) |
Cogan syndrome | (Orphanet:1467) |
Congenital contractural arachnodactyly | (Orphanet:115) |
Distal 22q11.2 microdeletion syndrome | (Orphanet:261330) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome with periventricular heterotopia | (Orphanet:82004) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Fabry disease | (Orphanet:324) |
Fragile X syndrome | (Orphanet:908) |
Giant cell arteritis | (Orphanet:397) |
Kawasaki disease | (Orphanet:2331) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
Lethal restrictive dermopathy | (Orphanet:1662) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
MARFANOID HABITUS WITH SITUS INVERSUS | (OMIM:609008) |
Marfan syndrome | (Orphanet:558) |
Marfan syndrome type 1 | (Orphanet:284963) |
Noonan syndrome | (Orphanet:648) |
PHACE syndrome | (Orphanet:42775) |
Relapsing polychondritis | (Orphanet:728) |
Takayasu arteritis | (Orphanet:3287) |
Zimmermann-Laband syndrome | (Orphanet:3473) |