DISEASES

Disease-gene associations mined from literature

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

Linkouts:  OMIM