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| Term | cerebral amyloid angiopathy | ID (Ontology) | DOID:9246 (Human Disease) |
| Definition | An amyloidosis where amyloid protein progressively deposits in cerebral blood vessel walls with subsequent degenerative vascular changes that usually result in spontaneous cerebral hemorrhage, ischemic lesions and progressive dementia. | ||
| Also Known As | "Cerebral Hemorrhage, Hereditary, with Amyloidosis" ; "Hereditary Cerebral Hemorrhage with Amyloidosis" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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disease of metabolism |__inherited metabolic disorder__ |__amyloidosis___________________| genetic disease | |__inherited metabolic disorder__| cerebral amyloid angiopathy 11 rec. |__APP-related cerebral amyloid angiopathy 2 rec. |__CST3-related cerebral amyloid angiopathy 3 rec. |__ITM2B-related cerebral amyloid angiopathy 1 3 rec. |__ITM2B-related cerebral amyloid angiopathy 2 3 rec. |
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| Is a |
inherited metabolic disorder amyloidosis |
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MESH:D028243 ORDO:85458 SNOMEDCT_US_2023_03_01:45639009 UMLS_CUI:C0268393 UMLS_CUI:C1510489 UMLS_CUI:C1527338 UMLS_CUI:C1956349 |
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