Term Name: CST3-related cerebral amyloid angiopathy
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.
Ontology: Human Disease [DOID:0070027]   ( DOID:0070027 )

Relationships
is a type of: autosomal dominant disease cerebral amyloid angiopathy