Aneurysm
Symptom Information:
Symptom ID: | HPO:0002617 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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) Aneurysm(HPO:0002617) MedDRA: |
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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) |