loading...| Preferred Name |
CADASIL [Disease/Finding] |
|
| Synonyms |
Dementia, Hereditary Multi-Infarct Type |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000010974 |
|
| altLabel |
Dementia, Hereditary Multi-Infarct Type CADASIL Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy |
|
| cui |
C0751587 |
|
| MESH DEFINITION |
A familial, cerebral arteriopathy mapped to chromosome 19q12, and characterized by the presence of granular deposits in small CEREBRAL ARTERIES producing ischemic STROKE; PSEUDOBULBAR PALSY; and multiple subcortical infarcts (CEREBRAL INFARCTION). CADASIL is an acronym for Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. CADASIL differs from BINSWANGER DISEASE by the presence of MIGRAINE WITH AURA and usually by the lack of history of arterial HYPERTENSION. (From Bradley et al, Neurology in Clinical Practice, 2000, p1146) |
|
| MESH DUI |
D046589 |
|
| MeSH name |
CADASIL |
|
| MESH UI |
M0334725 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000010974 |
|
| NUI |
N0000010974 |
|
| prefLabel |
CADASIL [Disease/Finding] |
|
| tui |
T047 |
|
| subClassOf |