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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

Xenbase Genes : app

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011583 - cerebral amyloid angiopathy, APP-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)