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Echinobase
Summary Literature (0)
DOID:0070027 - CST3-related cerebral amyloid angiopathy

Disease Ontology Definition:A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of CST3 on chromosome 20p11.21.

Synonyms: Amyloidosis VI, Amyloidosis, Cerebroarterial, Icelandic Type, Cerebral Hemorrhage, Hereditary, with Amyloidosis, HCHWA, Hereditary Cerebral Hemorrhage with Amyloidosis,

Echinobase Genes :


OMIM:
MIM:105150 - cerebral amyloid angiopathy, cst3-related

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): cerebral amyloid angiopathy (is_a)