Cerebral infarction
Symptom Information:
Symptom ID: | MedDRA:10008118 | ||
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Is a (Whole tree): |
HPO:
MedDRA: Vascular disorders(MedDRA:10047065) Arteriosclerosis, stenosis, vascular insufficiency and necrosis(MedDRA:10003216) Cerebrovascular and spinal necrosis and vascular insufficiency(MedDRA:10008192) Cerebral infarction(MedDRA:10008118) |
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Database Frequency: | 10 / 7739 | ||
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All diseases associated with this symptom:
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
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) |
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism | (Orphanet:280679) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Sneddon syndrome | (Orphanet:820) |