Arterial dissection

Symptom Information:

Symptom ID: HPO:0005294
Arterial rupture [Orphanet:35630]
Rupture of artery (disorder) [Orphanet:35630]
Rupture of artery [Orphanet:35630]
Arterial dissection [OMIM:Arterial dissection]
Arterial rupture [OMIM:Arterial rupture]
Arterial rupture [MedDRA:10003173]
Cross references:
Orphanet:35630 "Arterial rupture" [Orphanet:35630]
OMIM: "Arterial dissection" [OMIM:Arterial dissection]
OMIM: "Arterial rupture" [OMIM:Arterial rupture]
UMLS:C0155760 "Rupture of artery" [Orphanet:35630]
Is a (Direct Parents):
MedDRA Non-site specific vascular disorders NEC
HPO         Abnormality of the systemic arterial tree
Orphanet Abnormality of cardiovascular system physiology
Is a (Whole tree): HPO:
    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)
                Arterial dissection(HPO:0005294)
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Non-site specific vascular disorders NEC(MedDRA:10047067)
          Arterial dissection(HPO:0005294)
Database Frequency: 8 / 7739

All diseases associated with this symptom:

Arterial dissection - lentiginosis (Orphanet:1682)
Connective tissue disorder due to lysyl hydroxylase-3 deficiency (Orphanet:300284)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Ehlers-Danlos syndrome, kyphoscoliotic type (Orphanet:1900)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
Marfan syndrome (Orphanet:558)