Term Name:	autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 2
Synonyms:
Definition:	A CADASIL characterized by alopecia, spondylosis, and progressive motor dysfunction and dementia. Onset is usually in the second or third decade that has_material_basis_in homozygous or compound heterozygous mutation in the HTRA1 gene on chromosome 10q26.
Ontology:	Human Disease [DOID:0061228]   ( DOID:0061228 )