Cerebral ischemia
Symptom Information:
| Symptom ID: | HPO:0002637 | ||||
| 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 systemic arterial tree(HPO:0011004) Abnormalities of the peripheral arteries(HPO:0005114) Arterial stenosis(HPO:0100545) Cerebral ischemia(HPO:0002637) Abnormality of cerebral artery(HPO:0009145) Cerebral ischemia(HPO:0002637) Abnormality of the cerebral vasculature(HPO:0100659) Abnormality of cerebral artery(HPO:0009145) Cerebral ischemia(HPO:0002637) MedDRA: |
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| Database Frequency: | 17 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| CADASIL | (Orphanet:136) |
| Carney complex | (Orphanet:1359) |
| Cerebroretinal vasculopathy | (Orphanet:3421) |
| HERNS syndrome | (Orphanet:63261) |
| Hereditary cerebral hemorrhage with amyloidosis, Arctic type | (Orphanet:324723) |
| Hereditary cerebral hemorrhage with amyloidosis, Dutch type | (Orphanet:100006) |
| Hereditary cerebral hemorrhage with amyloidosis, Flemish type | (Orphanet:324718) |
| 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 vascular retinopathy | (Orphanet:71291) |
| INTERNAL CAROTID ARTERIES, HYPOPLASIA OF | (OMIM:243100) |
| MELAS | (Orphanet:550) |
| Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
| Polycythemia vera | (Orphanet:729) |
| Retinal vasculopathy and cerebral leukodystrophy | (Orphanet:247691) |
| Thiamine-responsive megaloblastic anemia syndrome | (Orphanet:49827) |