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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 the CST3 gene on chromosome 20p11.21.

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

Echinobase Genes :


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

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

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