Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
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, Cerebroarterial, Icelandic Type, Amyloidosis VI, 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

Xenbase Genes : cst3

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007098 - mandibular neural crest

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)