"ICD10CM:F01.1"^^ . "OMIM:616779"^^ . _:vb50944090 . "CADASIL 2"^^ . "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."^^ . _:vb50944090 . _:vb50944090 . "DOID:0111036"^^ . . "autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2"@en . "disease_ontology"^^ . . . . _:vb50944090 . _:vb50944090 .