CADASIL 1 (Q32146322)
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CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13
- autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1
- CADASIL type 1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | CADASIL 1 |
CADASIL characterized by migraine, strokes, and white matter lesions that has material basis in heterozygous mutation in the NOTCH3 gene on chromosome 19p13 |
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Statements
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1 reference
Identifiers
1 reference
2 references
1 reference