Cerebral aneurysm
Symptom Information:
Symptom ID: | HPO:0004944 | |||||||
Synonyms: |
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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) Abnormality of the systemic arterial tree(HPO:0011004) Abnormality of cerebral artery(HPO:0009145) Cerebral aneurysm(HPO:0004944) Aneurysm(HPO:0002617) Cerebral aneurysm(HPO:0004944) Abnormality of the cerebral vasculature(HPO:0100659) Abnormality of cerebral artery(HPO:0009145) Cerebral aneurysm(HPO:0004944) MedDRA: Vascular disorders(MedDRA:10047065) Aneurysms and artery dissections(MedDRA:10002363) Cerebrovascular aneurysms and dissections(MedDRA:10008194) Cerebral aneurysm(HPO:0004944) |
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Database Frequency: | 12 / 7739 | |||||||
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All diseases associated with this symptom:
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures | (Orphanet:73229) |
Connective tissue disorder due to lysyl hydroxylase-3 deficiency | (Orphanet:300284) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Familial cerebral saccular aneurysm | (Orphanet:231160) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
LOEYS-DIETZ SYNDROME 1 | (OMIM:609192) |
LOEYS-DIETZ SYNDROME 2 | (OMIM:610168) |
Loeys-Dietz syndrome type 1 | (Orphanet:60030) |
MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME | (OMIM:613834) |
Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
POLYCYSTIC KIDNEY DISEASE 1 | (OMIM:173900) |