FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term CADASIL ID (Ontology) DOID:13945 (Human Disease)
Definition A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment.
Also Known As "cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy" ; "hereditary multi-infarct dementia"
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 Genes
 CADASIL       1
 for disease ribbon | CADASIL       1
 model of | CADASIL       1
Spanning Tree (Parents/Children)
Only view relationship: 
  cerebral degeneration
   |__leukodystrophy
       |__CADASIL  2 rec.
           |__CADASIL 1 1 rec.
           |__CADASIL 2 1 rec.
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Is a leukodystrophy
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Synonyms
  • "cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy" EXACT
    "hereditary multi-infarct dementia" EXACT
Secondary IDs
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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