Aortic root dilatation

Symptom Information:

Symptom ID: HPO:0002616
Synonyms:
increased aortic root diameter [HPO:0002616]
Aneurysm of the aortic sinus [Orphanet:34620]
Aortic root dilatation (disorder) [Orphanet:34620]
Congenital aneurysm of sinus of Valsalva (disorder) [Orphanet:34620]
Congenital aneurysm of sinus of Valsalva [Orphanet:34620]
Aortic root dilatation [Orphanet:34620]
Aortic root dilatation [OMIM:Aortic root dilatation]
Aortic root dilatation/dilation/aneurysm [Orphanet:34620]
Quality:
Cross references:
Orphanet:34620 "Aortic root dilatation/dilation/aneurysm" [Orphanet:34620]
OMIM: "Aortic root dilatation" [OMIM:Aortic root dilatation]
UMLS:C0265893 "Congenital aneurysm of sinus of Valsalva" [Orphanet:34620]
UMLS:C0238669 "Aortic root dilatation" [Orphanet:34620]
Is a (Direct Parents):
Orphanet Structural anomalies of the cardio-circulatory system
HPO         Dilatation of the ascending aorta
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)