Human genes for CADASIL 2
CADASIL 2 [DOID:0111036]
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.
Synonyms: CADASIL 2, DOID:0111036, autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2