Search Ontology:
Human Disease

CADASIL

Term ID
DOID:13945
Synonyms
  • 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
  • GARD:1049
  • ICD10CM:I67.850
  • MESH:D046589
  • MIM:PS125310
  • NCI:C84606
  • ORDO:136
  • SNOMEDCT_US_2023_03_01:390723008
  • UMLS_CUI:C0751587
Ontology
Human Disease   ( DOID:13945 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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