Stroke

Symptom Information:

Symptom ID: HPO:0001297
Synonyms:
Cerebral vascular events [HPO:0001297]
Cerebrovascular accident [HPO:0001297]
CEREBROVASCULAR ACCIDENTS [HPO:0001297]
Ischemic stroke [Orphanet:43110]
Ischemic stroke (disorder) [Orphanet:43110]
Cerebral vascular events [OMIM:Cerebral vascular events]
Cerebrovascular accident [OMIM:Cerebrovascular accident]
Cerebrovascular accidents [OMIM:Cerebrovascular accidents]
Stroke [OMIM:Stroke]
Transient cerebral ischemia/stroke [Orphanet:43110]
Ischaemic stroke [Orphanet:43110]
Cerebrovascular accident [Orphanet:43110]
Ischaemic stroke [MedDRA:10061256]
Ischaemic stroke NOS [MedDRA:10061256]
Ischemic stroke [MedDRA:10061256]
Cerebrovascular accident [MedDRA:10008190]
Accident cerebrovascular [MedDRA:10008190]
Apoplexy [MedDRA:10008190]
Cerebrovascular accident NOS [MedDRA:10008190]
CVA [MedDRA:10008190]
Middle cerebral artery stroke [MedDRA:10008190]
Stroke [MedDRA:10008190]
Worsening of stroke [MedDRA:10008190]
Late effects of cerebral stroke [MedDRA:10008190]
Apoplectic fit [MedDRA:10008190]
Cerebrovascular accident (in some patients) [OMIM:Cerebrovascular accident (in some patients)]
Stroke (in some patients) [OMIM:Stroke (in some patients)]
Stroke (rare) [OMIM:Stroke (rare)]
Stroke (uncommon) [OMIM:Stroke (uncommon)]
Strokes [OMIM:Strokes]
Quality:
Cross references:
HPO:0002140 "Ischemic stroke" [Orphanet:43110]
Orphanet:43110 "Transient cerebral ischemia/stroke" [Orphanet:43110]
OMIM: "Cerebral vascular events" [OMIM:Cerebral vascular events]
OMIM: "Cerebrovascular accident" [OMIM:Cerebrovascular accident]
OMIM: "Cerebrovascular accidents" [OMIM:Cerebrovascular accidents]
OMIM: "Stroke" [OMIM:Stroke]
OMIM: "Cerebrovascular accident (in some patients)" [OMIM:Cerebrovascular accident (in some patients)]
OMIM: "Stroke (in some patients)" [OMIM:Stroke (in some patients)]
OMIM: "Stroke (rare)" [OMIM:Stroke (rare)]
OMIM: "Stroke (uncommon)" [OMIM:Stroke (uncommon)]
OMIM: "Strokes" [OMIM:Strokes]
UMLS:C0038454 "Stroke" [HPO:0001297]
UMLS:C0948008 "Ischemic stroke" [Orphanet:43110]
Is a (Direct Parents):
MedDRA Cerebrovascular and spinal necrosis and vascular insufficiency
MedDRA Cerebrovascular and spinal vascular disorders NEC
HPO         Abnormality of the cerebral vasculature
Orphanet Functional anomalies of the nervous system
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 cerebral vasculature(HPO:0100659)
                Stroke(HPO:0001297)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216)
       Cerebrovascular and spinal necrosis and vascular insufficiency(MedDRA:10008192)
          Stroke(HPO:0001297)
    Vascular disorders NEC(MedDRA:10047066)
       Cerebrovascular and spinal vascular disorders NEC(MedDRA:10008193)
          Stroke(HPO:0001297)
Database Frequency: 44 / 7739
Resource:

All diseases associated with this symptom:

ABDOMINAL OBESITY-METABOLIC SYNDROME 3 (OMIM:615812)
AORTIC ANEURYSM, FAMILIAL THORACIC 4 (OMIM:132900)
Acyl-CoA dehydrogenase 9 deficiency (Orphanet:99901)
Alagille syndrome due to 20p12 microdeletion (Orphanet:261600)
Alagille syndrome due to a JAG1 point mutation (Orphanet:261619)
Atrial fibrillation, familial, 3 (OMIM:607554)
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures (Orphanet:73229)
Barth syndrome (Orphanet:111)
CADASIL (Orphanet:136)
CEREBRAL CAVERNOUS MALFORMATIONS 2 (OMIM:603284)
Carbamoylphosphate synthetase deficiency (Orphanet:147)
Cardiomyopathy, dilated, 1E (OMIM:601154)
Cardiomyopathy, dilated, 1S (OMIM:613426)
Carney complex (Orphanet:1359)
Cerebroretinal vasculopathy (Orphanet:3421)
Chuvash erythrocytosis (Orphanet:238557)
Citrullinemia type I (Orphanet:247525)
Classical homocystinuria (Orphanet:394)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Fabry disease (Orphanet:324)
Familial isolated dilated cardiomyopathy (Orphanet:154)
Fibromuscular dysplasia of arteries (Orphanet:336)
HERNS syndrome (Orphanet:63261)
Hereditary cerebral hemorrhage with amyloidosis, Dutch type (Orphanet:100006)
Hereditary cerebral hemorrhage with amyloidosis, Icelandic type (Orphanet:100008)
Hereditary vascular retinopathy (Orphanet:71291)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency (Orphanet:395)
JUVENILE POLYPOSIS/HEREDITARY HEMORRHAGIC TELANGIECTASIA SYNDROME (OMIM:175050)
Leigh syndrome (Orphanet:506)
MELAS (Orphanet:550)
Malignant atrophic papulosis (Orphanet:679)
Nodular neuronal heterotopia (Orphanet:2149)
Ornithine transcarbamylase deficiency (Orphanet:664)
Papillary fibroelastoma of the heart (Orphanet:208600)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
STROKE, ISCHEMIC (OMIM:601367)
Sneddon syndrome (Orphanet:820)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
WOLFF-PARKINSON-WHITE SYNDROME (OMIM:194200)
Williams syndrome (Orphanet:904)
[DEL] PSEUDOXANTHOMA ELASTICUM (OMIM:264800)