CADASIL 1

Summary

DOID:0111035 - CADASIL 1

Disease Ontology Definition:A CADASIL characterized by migraine, strokes, and white matter lesions that has_material_basis_in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.

Synonyms: autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: notch3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0000914 - cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1

MONDO:0000914 - cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), CADASIL (is_a)