Stroke
Symptom Information:
Symptom ID: | HPO:0001297 | ||||||||||||||||||||||||||||||
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) 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) |
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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) |