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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
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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)