Human genes for antithrombin III deficiency
Antithrombin III deficiency [DOID:3755]
Antithrombin III deficiency is a rare hereditary disorder that generally comes to light when a patient suffers recurrent venous thrombosis and pulmonary embolism. Inheritance is usually autosomal dominant, though a few recessive cases have been noted.
Synonyms: antithrombin III deficiency, DOID:3755