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Disease Ontology Browser
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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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11/19/2024
MGI 6.24 		The Jackson Laboratory