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:3755 - antithrombin III deficiency

Disease Ontology Definition:A thrombophilia that is characterized by the tendency to form clots in the veins.

Synonyms: AT III deficiency, hereditary thrombophilia due to congenital antithrombin deficiency,

Xenbase Genes : serpinc1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013144 - hereditary antithrombin deficiency


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

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