Term Name:	CADASIL 2
Synonyms:	autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2
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.
Ontology:	Human Disease [DOID:0111036]   ( DOID:0111036 )