Cerebral ischemia
Symptom Information:
Symptom ID: | HPO:0002637 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
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) Abnormality of the systemic arterial tree(HPO:0011004) Abnormality of cerebral artery(HPO:0009145) Cerebral ischemia(HPO:0002637) Abnormalities of the peripheral arteries(HPO:0005114) Arterial stenosis(HPO:0100545) Cerebral ischemia(HPO:0002637) MedDRA: |
||||
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) |