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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: Alliance, 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)