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Disease Ontology Browser
CADASIL 2 (DOID:0111036)
Alliance: disease page
Synonyms: autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2
Alt IDs: OMIM:616779, ICD10CM:F01.1
Definition: A CADASIL characterized by stroke, transient ischemic attacks, cognitive impairment, dementia, balance impairment, gait disturbance, headaches, and/or seizures associated with early confluent or confluent diffuse white matter hyperintensities that has_material_basis_in heterozygous mutation in the HTRA1 gene on chromosome 10q26.

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
12/10/2024
MGI 6.24 		The Jackson Laboratory