About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory