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Summary Literature (1)
DOID:13945 - CADASIL

Disease Ontology Definition:A leukodystrophy characterized by recurrent subcortical ischemic stroke and cognitive impairment.

Synonyms: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, hereditary multi-infarct dementia,

Xenbase Genes : htra1, notch3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007432 - cerebral arteriopathy with subcortical infarcts and leukoencephalopathy


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): leukodystrophy (is_a)