Search Ontology:
Human Disease
CADASIL
- Term ID
- DOID:13945
- Synonyms
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- cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- hereditary multi-infarct dementia
- Definition
- A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment. (2)
- References
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- GARD:1049
- ICD10CM:I67.850
- MESH:D046589
- MIM:600142
- MIM:PS125310
- NCI:C84606
- ORDO:136
- SNOMEDCT_US_2023_03_01:390723008
- UMLS_CUI:C0751587
- Ontology
- Human Disease ( DOID:13945 )
- is a type of
-
- has subtype
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Other Pages
Genes Involved
Zebrafish Models