OBO ID: DOID:0111035
Term Name: CADASIL 1 Search Ontology:
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 CADASIL 1 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NOTCH3 Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1 125310
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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