Search Ontology:
Human Disease

CST3-related cerebral amyloid angiopathy

Term ID
DOID:0070027
Synonyms
  • Amyloidosis VI
  • Amyloidosis, Cerebroarterial, Icelandic Type
  • Cerebral Hemorrhage, Hereditary, with Amyloidosis
  • Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant
  • HCHWA
  • Hereditary Cerebral Hemorrhage with Amyloidosis
  • Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant
Definition
A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of the CST3 gene on chromosome 20p11.21. https://www.ncbi.nlm.nih.gov/pubmed/2900981
References
Ontology
Human Disease   ( DOID:0070027 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models