Cerebral infarction

Symptom Information:

Symptom ID: MedDRA:10008118
Synonyms:
Cerebral infarction [OMIM:Cerebral infarction]
Quality:
Cross references:
OMIM: "Cerebral infarction" [OMIM:Cerebral infarction]
Is a (Direct Parents):
MedDRA Cerebrovascular and spinal necrosis and vascular insufficiency
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)
Database Frequency: 10 / 7739
Resource:

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)