Term Name:	CADASIL 1
Synonyms:	autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 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.
Ontology:	Human Disease [DOID:0111035]   ( DOID:0111035 )