FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
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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DO.org
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Data Class Field Records
Human Disease Models (FBhh)  DOID       2
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 Genes Human Disease Models
 cerebral amyloid angiopathy       1      2
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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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Synonyms
  • "Cerebral Hemorrhage, Hereditary, with Amyloidosis" EXACT
    "Hereditary Cerebral Hemorrhage with Amyloidosis" EXACT
Secondary IDs
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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