Search Ontology:
Human Disease

APP-related cerebral amyloid angiopathy

Term ID
DOID:0070028
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 Pages
Genes Involved
Zebrafish Models