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Metadata
ID DOID:0070027
Name CST3-related cerebral amyloid angiopathy
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
Xrefs

OMIM:105150

Synonyms

Amyloidosis VI [EXACT]

Amyloidosis, Cerebroarterial, Icelandic Type [EXACT]

Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant [EXACT]

HCHWA [EXACT]

Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant [EXACT]

Parent Relationships

is_a cerebral amyloid angiopathy

is_a autosomal dominant disease

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