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Disease Ontology Browser
CADASIL (DOID:13945)
Alliance: disease page
Synonyms: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; hereditary multi-infarct dementia
Alt IDs: OMIM:600142, ICD10CM:I67.850, MESH:D046589, NCI:C84606, OMIM:PS125310, ORDO:136, UMLS_CUI:C0751587
Definition: A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment.

Disease References using Mouse Models (9)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory