Cerebral aneurysm

Symptom Information:

Symptom ID: HPO:0004944
Synonyms:
Cerebral artery aneurysm [HPO:0004944]
Intracranial aneurysm [HPO:0004944]
Cerebral aneurysm [OMIM:Cerebral aneurysm]
Cerebral artery aneurysm [OMIM:Cerebral artery aneurysm]
Intracranial aneurysm [OMIM:Intracranial aneurysm]
Cerebral aneurysm (uncommon) [OMIM:Cerebral aneurysm (uncommon)]
Intracranial aneurysm [MedDRA:10022758]
Quality:
Cross references:
OMIM: "Cerebral aneurysm" [OMIM:Cerebral aneurysm]
OMIM: "Cerebral artery aneurysm" [OMIM:Cerebral artery aneurysm]
OMIM: "Intracranial aneurysm" [OMIM:Intracranial aneurysm]
OMIM: "Cerebral aneurysm (uncommon)" [OMIM:Cerebral aneurysm (uncommon)]
Is a (Direct Parents):
MedDRA Cerebrovascular aneurysms and dissections
HPO         Abnormality of cerebral artery
HPO         Aneurysm
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)
             Abnormality of the cerebral vasculature(HPO:0100659)
                Abnormality of cerebral artery(HPO:0009145)
                   Cerebral aneurysm(HPO:0004944)
             Aneurysm(HPO:0002617)
                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)
Database Frequency: 12 / 7739
Resource:

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)