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:0080348 - Alzheimer's disease 1

Disease Ontology Definition:An Alzheimer's disease that has_material_basis_in mutation heterozygous mutation in the APP gene, which encodes the amyloid precursor protein, on chromosome 21q21.

Synonyms: Alzheimer's disease 1, early onset,

Xenbase Genes : app, ace, paxip1, nos3, a2m, mpo, apbb2, sorl1, blmh



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

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