Transient ischemic attack
Symptom Information:
Symptom ID: | HPO:0002326 | ||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Transient ischemic attack(HPO:0002326) Stroke(HPO:0001297) Transient ischemic attack(HPO:0002326) Abnormality of the systemic arterial tree(HPO:0011004) Abnormalities of the peripheral arteries(HPO:0005114) Arterial stenosis(HPO:0100545) Cerebral ischemia(HPO:0002637) Transient ischemic attack(HPO:0002326) Abnormality of cerebral artery(HPO:0009145) Cerebral ischemia(HPO:0002637) Transient ischemic attack(HPO:0002326) MedDRA: Nervous system disorders(MedDRA:10029205) Central nervous system vascular disorders(MedDRA:10007963) Transient cerebrovascular events(MedDRA:10044376) Transient ischemic attack(HPO:0002326) |
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Database Frequency: | 13 / 7739 | ||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
CADASIL | (Orphanet:136) |
Carney complex | (Orphanet:1359) |
Fabry disease | (Orphanet:324) |
HERNS syndrome | (Orphanet:63261) |
Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
MELAS | (Orphanet:550) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Sneddon syndrome | (Orphanet:820) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, OF RENDU, OSLER, AND WEBER | (OMIM:187300) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 2 | (OMIM:600376) |
TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 4 | (OMIM:610655) |
Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |
Toriello-Lacassie-Droste syndrome | (Orphanet:3339) |