Ischemic stroke
Symptom Information:
Symptom ID: | HPO:0002140 | ||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): | |||||||||||||||||||||||||
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) Abnormality of cerebral artery(HPO:0009145) Cerebral ischemia(HPO:0002637) Ischemic stroke(HPO:0002140) Stroke(HPO:0001297) Ischemic stroke(HPO:0002140) 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) 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) |
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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) |