OBO ID: DOID:0070028
Term Name: APP-related cerebral amyloid angiopathy Search Ontology:
Synonyms:
  • Amyloidosis, Cerebroarterial, App-Related
  • Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant
  • Cerebral Amyloid Angiopathy, App-Related, Arctic Variant
  • Cerebral Amyloid Angiopathy, App-Related, Dutch Variant
  • Cerebral Amyloid Angiopathy, App-Related, Flemish Variant
  • Cerebral Amyloid Angiopathy, App-Related, Iowa Variant
  • Cerebral Amyloid Angiopathy, App-Related, Italian Variant
  • HCHWAD
Definition: A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of APP on chromosome 21q21.3. https://www.ncbi.nlm.nih.gov/pubmed/2111584
References:
Ontology: Human Disease   ( DOID:0070028 )
Relationships
is a type of:
OTHER APP-related cerebral amyloid angiopathy PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
APP Cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants 605714
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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