Cadasil
Disease ID: disease_node_11298
Connections displayed (default: 10).
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| Dbxref | GARD:1049, ICD10CM:I67.850, MESH:D046589, MIM:600142, MIM:PS125310, NCI:C84606, ORDO:136, SNOMEDCT_US_2023_03_01:390723008, UMLS_CUI:C0751587 |
|---|---|
| Subclassof | DOID_10579 |
| Data Source | DOID, MESH |
| Synonyms | cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, hereditary multi-infarct dementia |
| Mesh Id | D046589 |
| Mesh Label | CADASIL |
| Mesh Subclassof | D030342, D015140, D002544, D059345, D002539 |
| Doid Label | CADASIL |
| Doid Description | A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment. |
| Disease Node Id | disease_node_11298 |
| Doid Id | DOID_13945 |
| Label | Cadasil |
- Outgoing r'ship
SUBCLASS_OFto/from Leukodystrophy(ID:disease_node_19911) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Cadasil 2(ID:disease_node_19912) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Cadasil 1(ID:disease_node_19913) (Disease)