FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term APP-related cerebral amyloid angiopathy ID (Ontology) DOID:0070028 (Human Disease)
Definition A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of APP on chromosome 21q21.3.
Also Known As "Amyloidosis, Cerebroarterial, App-Related" ; "Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant" ; "Cerebral Amyloid Angiopathy, App-Related, Arctic Variant" (for all, see Synonyms field below)
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 APP-related cerebral amyloid angiopathy       1      1
 for disease ribbon | APP-related cerebral amyloid angiopathy       1       --
 model of | APP-related cerebral amyloid angiopathy       1       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease___
inherited metabolic disorder     |
 |__cerebral amyloid angiopathy__|
amyloidosis                      |
 |__cerebral amyloid angiopathy__|
                                 APP-related cerebral amyloid angiopathy  2 rec.
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Is a autosomal dominant disease
cerebral amyloid angiopathy
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Synonyms
  • "Amyloidosis, Cerebroarterial, App-Related" EXACT
    "Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant" EXACT
    "Cerebral Amyloid Angiopathy, App-Related, Arctic Variant" EXACT
    "Cerebral Amyloid Angiopathy, App-Related, Dutch Variant" EXACT
    "Cerebral Amyloid Angiopathy, App-Related, Flemish Variant" EXACT
    "Cerebral Amyloid Angiopathy, App-Related, Iowa Variant" EXACT
    "Cerebral Amyloid Angiopathy, App-Related, Italian Variant" EXACT
    "HCHWAD" EXACT OMO:0003012
Secondary IDs
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MIM:605714