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Disease Ontology Browser
CADASIL 1 (DOID:0111035)
Alliance: disease page
Synonyms: autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
Alt IDs: OMIM:125310, ICD10CM:F01.1
Definition: A CADASIL characterized by migraine, strokes, and white matter lesions that has_material_basis_in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.

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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last database update
01/24/2023
MGI 6.22
The Jackson Laboratory