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Disease Ontology Browser
antithrombin III deficiency (DOID:3755)
Alliance: disease page
Synonyms: AT III deficiency; hereditary thrombophilia due to congenital antithrombin deficiency
Alt IDs: OMIM:613118, ICD10CM:D68.59, MESH:D020152, NCI:C98815, UMLS_CUI:C0272375
Definition: An inherited blood coagulation disease characterized by the tendency to form clots in the veins.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory