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Summary Literature (0)
DOID:0070028 - APP-related cerebral amyloid angiopathy


Disease Ontology Definition:A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of APP on chromosome 21q21.3.

Synonyms: Amyloidosis, Cerebroarterial, App-Related, Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant, Cerebral Amyloid Angiopathy, App-Related, Arctic Variant, Cerebral Amyloid Angiopathy, App-Related, Dutch Variant, Cerebral Amyloid Angiopathy, App-Related, Flemish Variant, Cerebral Amyloid Angiopathy, App-Related, Iowa Variant, Cerebral Amyloid Angiopathy, App-Related, Italian Variant, HCHWAD

In OMIM:
OMIM:605714 - CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED

In Mondo Disease Ontology:
MONDO:0011583 - cerebral amyloid angiopathy, APP-related

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : app

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): cerebral amyloid angiopathy (is_a)