CST3-related cerebral amyloid angiopathy (DOID:0070027)
Alliance: disease page
Synonyms: Amyloidosis VI; Amyloidosis, Cerebroarterial, Icelandic Type; Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant; HCHWA; Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant
Alt IDs: OMIM:105150
Definition: A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of the CST3 gene on chromosome 20p11.21.