Ischemic stroke

Symptom Information:

Symptom ID: HPO:0002140
Synonyms:
Ischemic stroke (disorder) [Orphanet:43110]
Ischemic stroke [Orphanet:43110]
Ischemic stroke [OMIM:Ischemic 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:0001297 "Stroke" [Orphanet:43110]
Orphanet:43110 "Transient cerebral ischemia/stroke" [Orphanet:43110]
OMIM: "Ischemic stroke" [OMIM:Ischemic 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:C0948008 "Ischemic stroke" [Orphanet:43110]
Is a (Direct Parents):
Orphanet Functional anomalies of the nervous system
MedDRA Cerebrovascular and spinal necrosis and vascular insufficiency
MedDRA Cerebrovascular and spinal vascular disorders NEC
HPO         Cerebral ischemia
Orphanet Stroke
HPO         Stroke
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)
                Abnormalities of the peripheral arteries(HPO:0005114)
                   Arterial stenosis(HPO:0100545)
                      Cerebral ischemia(HPO:0002637)
                         Ischemic stroke(HPO:0002140)
                Abnormality of cerebral artery(HPO:0009145)
                   Cerebral ischemia(HPO:0002637)
                      Ischemic stroke(HPO:0002140)
             Abnormality of the cerebral vasculature(HPO:0100659)
                Abnormality of cerebral artery(HPO:0009145)
                   Cerebral ischemia(HPO:0002637)
                      Ischemic stroke(HPO:0002140)
                Stroke(HPO:0001297)
                   Ischemic stroke(HPO:0002140)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216)
       Cerebrovascular and spinal necrosis and vascular insufficiency(MedDRA:10008192)
          Ischemic stroke(HPO:0002140)
    Vascular disorders NEC(MedDRA:10047066)
       Cerebrovascular and spinal vascular disorders NEC(MedDRA:10008193)
          Ischemic stroke(HPO:0002140)
Database Frequency: 70 / 7739
Resource:

All diseases associated with this symptom:

AORTIC ANEURYSM, FAMILIAL THORACIC 4 (OMIM:132900)
Alveolar echinococcosis (Orphanet:284)
Arterial tortuosity syndrome (Orphanet:3342)
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures (Orphanet:73229)
Baraitser-Winter syndrome (Orphanet:2995)
Behçet disease (Orphanet:117)
Budd-Chiari syndrome (Orphanet:131)
CADASIL (Orphanet:136)
CEDNIK syndrome (Orphanet:66631)
Carbamoylphosphate synthetase deficiency (Orphanet:147)
Cardiomyopathy, dilated, 1E (OMIM:601154)
Carney complex (Orphanet:1359)
Cerebroretinal vasculopathy (Orphanet:3421)
Chronic hiccup (Orphanet:396)
Citrullinemia type I (Orphanet:247525)
Classical homocystinuria (Orphanet:394)
Cogan syndrome (Orphanet:1467)
Dystrophic epidermolysis bullosa (Orphanet:303)
Ebstein malformation (Orphanet:1880)
Ehlers-Danlos syndrome due to tenascin-X deficiency (Orphanet:230839)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Erythromelalgia (Orphanet:1956)
Essential thrombocythemia (Orphanet:3318)
Fabry disease (Orphanet:324)
Familial Mediterranean fever (Orphanet:342)
Familial atrial myxoma (Orphanet:615)
Familial thrombocytosis (Orphanet:71493)
Giant cell arteritis (Orphanet:397)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Glycogen storage disease due to acid maltase deficiency, late-onset (Orphanet:420429)
Granulomatosis with polyangiitis (Orphanet:900)
HERNS syndrome (Orphanet:63261)
Hereditary cerebral hemorrhage with amyloidosis, Dutch type (Orphanet:100006)
Hereditary cerebral hemorrhage with amyloidosis, Icelandic type (Orphanet:100008)
Hereditary cerebral hemorrhage with amyloidosis, Iowa type (Orphanet:324708)
Hereditary cerebral hemorrhage with amyloidosis, Italian type (Orphanet:324713)
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type (Orphanet:324703)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hereditary vascular retinopathy (Orphanet:71291)
Hypoalphalipoproteinemia (Orphanet:31153)
Incontinentia pigmenti (Orphanet:464)
Kawasaki disease (Orphanet:2331)
Liddle syndrome (Orphanet:526)
MELAS (Orphanet:550)
MOYAMOYA DISEASE 6 WITH ACHALASIA (OMIM:615750)
Malignant atrophic papulosis (Orphanet:679)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Methylmalonic acidemia without homocystinuria (Orphanet:293355)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Ornithine transcarbamylase deficiency (Orphanet:664)
PORENCEPHALY 1 (OMIM:175780)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Polycythemia vera (Orphanet:729)
Porencephaly (Orphanet:2940)
Primary familial polycythemia (Orphanet:90042)
Pseudoxanthoma elasticum (Orphanet:758)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
Secondary polycythemia (Orphanet:98428)
Sneddon syndrome (Orphanet:820)
Sturge-Weber syndrome (Orphanet:3205)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER (OMIM:187300)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 (OMIM:600376)
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 (OMIM:610655)
Takayasu arteritis (Orphanet:3287)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Thoracic outlet syndrome (Orphanet:97330)
Waldenström macroglobulinemia (Orphanet:33226)
Williams syndrome (Orphanet:904)