Term Name:	autosomal recessive cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1
Synonyms:
Definition:	A CADASIL characterized by the onset of neurologic symptoms in infancy or early childhood that has_material_basis_in homozygous or compound heterozygous mutations in the NOTCH3 gene on chromosome 19p13.
Ontology:	Human Disease [DOID:0061227]   ( DOID:0061227 )