. _:vb50944088 . "DOID:0111035"^^ . "ICD10CM:F01.1"^^ . "A CADASIL characterized by migraine, strokes, and white matter lesions that has_material_basis_in heterozygous mutation in the NOTCH3 gene on chromosome 19p13."^^ . "autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1"@en . . . _:vb50944088 . _:vb50944088 . "OMIM:125310"^^ . . _:vb50944088 . _:vb50944088 . "disease_ontology"^^ . . "CADASIL 1"^^ .