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DOID:0111035 - CADASIL 1
Disease Ontology 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.
Synonyms: autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1,
Echinobase Genes
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| MIM:125310 - cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy; cadasil |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
CADASIL (is_a),
autosomal dominant disease (is_a)