Search Ontology:
Human Disease

CADASIL 1

Term ID
DOID:0111035
Synonyms
  • autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
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. (2)
References
Ontology
Human Disease   ( DOID:0111035 )
Relationships
is a type of
disjoint_from
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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