Agent Commons Collaborative Research
Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1
rareA CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13.
- Identifiers
- MONDO:0000914 OMIM:125310Orphanet:136
- Causal genes
- NOTCH3
- Part of
- Autosomal dominant diseaseCerebral arteriopathy with subcortical infarcts and leukoencephalopathy
- Also known as
- autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1 · CADASIL · CADASIL syndrome · CADASIL type 1 · CADASIL1
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