Abnormality of the cerebral vasculature
Symptom Information:
| Symptom ID: | HPO:0100659 | ||||
| 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) MedDRA: |
||||
| Database Frequency: | 25 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| 3M syndrome | (Orphanet:2616) |
| Autoimmune polyendocrinopathy type 1 | (Orphanet:3453) |
| Celiac disease, epilepsy and cerebral calcification syndrome | (Orphanet:1459) |
| Cerebral arteriovenous malformation | (Orphanet:46724) |
| Essential thrombocythemia | (Orphanet:3318) |
| GAPO syndrome | (Orphanet:2067) |
| Hereditary cerebral hemorrhage with amyloidosis, Icelandic type | (Orphanet:100008) |
| Hereditary cerebral hemorrhage with amyloidosis, Iowa type | (Orphanet:324708) |
| Hereditary cerebral hemorrhage with amyloidosis, Piedmont type | (Orphanet:324703) |
| Hereditary hemorrhagic telangiectasia | (Orphanet:774) |
| Hereditary thrombophilia due to congenital protein C deficiency | (Orphanet:745) |
| Hereditary thrombophilia due to congenital protein S deficiency | (Orphanet:743) |
| Holoprosencephaly - caudal dysgenesis | (Orphanet:2165) |
| Isolated 3-methylcrotonyl-CoA carboxylase deficiency | (Orphanet:6) |
| Lymphedema - cerebral arteriovenous anomaly | (Orphanet:86914) |
| Microcephalic osteodysplastic primordial dwarfism type 2 | (Orphanet:2637) |
| Moyamoya disease | (Orphanet:2573) |
| Pseudoxanthoma elasticum | (Orphanet:758) |
| Secondary polycythemia | (Orphanet:98428) |
| Sneddon syndrome | (Orphanet:820) |
| Sturge-Weber syndrome | (Orphanet:3205) |
| Vein of Galen aneurysm | (Orphanet:1053) |
| Von Hippel-Lindau disease | (Orphanet:892) |
| Werner syndrome | (Orphanet:902) |
| Williams syndrome | (Orphanet:904) |