Aneurysm

Symptom Information:

Symptom ID: HPO:0002617
Synonyms:
Aneurysmal disease [HPO:0002617]
Aneurysms (internal carotid artery, cerebral artery, subclavian) [OMIM:Aneurysms (internal carotid artery, cerebral artery, subclavian)]
Quality:
Cross references:
OMIM: "Aneurysms (internal carotid artery, cerebral artery, subclavian)" [OMIM:Aneurysms (internal carotid artery, cerebral artery, subclavian)]
UMLS:C0002940 "Aneurysm" [HPO:0002617]
Is a (Direct Parents):
HPO         Abnormality of the vasculature
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)
             Aneurysm(HPO:0002617)
MedDRA:
Database Frequency: 34 / 7739
Resource:

All diseases associated with this symptom:

Arrhythmogenic right ventricular dysplasia, familial, 10 (OMIM:610193)
Arrhythmogenic right ventricular dysplasia, familial, 4 (OMIM:602087)
Arrhythmogenic right ventricular dysplasia, familial, 6 (OMIM:604401)
Arrhythmogenic right ventricular dysplasia, familial, 9 (OMIM:609040)
Arterial tortuosity syndrome (Orphanet:3342)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis (OMIM:615821)
Cogan syndrome (Orphanet:1467)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Fabry disease (Orphanet:324)
Glycogen storage disease due to acid maltase deficiency, infantile onset (Orphanet:308552)
Hughes-Stovin syndrome (Orphanet:228116)
Interventricular septum aneurysm (Orphanet:99092)
Isolated polycystic liver disease (Orphanet:2924)
Kawasaki disease (Orphanet:2331)
Loeys-Dietz syndrome type 1 (Orphanet:60030)
Marfan syndrome (Orphanet:558)
Menkes disease (Orphanet:565)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Multiple osteochondromas (Orphanet:321)
Noonan syndrome with multiple lentigines (Orphanet:500)
Occipital horn syndrome (Orphanet:198)
Orofaciodigital syndrome type 1 (Orphanet:2750)
PHACE syndrome (Orphanet:42775)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Pseudoxanthoma elasticum (Orphanet:758)
Relapsing polychondritis (Orphanet:728)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
Takayasu arteritis (Orphanet:3287)
Tuberous sclerosis (Orphanet:805)
Vein of Galen aneurysm (Orphanet:1053)
Wyburn-Mason syndrome (Orphanet:53719)