OBO ID: DOID:0070027 |
Term Name: | CST3-related cerebral amyloid angiopathy | Search Ontology: | |
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Definition: | A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of the CST3 gene on chromosome 20p11.21. https://www.ncbi.nlm.nih.gov/pubmed/2900981 | ||
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Ontology: | Human Disease ( DOID:0070027 ) |
OTHER CST3-related cerebral amyloid angiopathy PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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