C98815Level 6
Antithrombin III Deficiency
**Semantic type:** Disease or Syndrome
**Definition:** A rare disorder characterized by the presence of low levels of antithrombin III which prohibits the formation of blood clots. It may be inherited, usually in an autosomal dominant pattern, or acquired. It may lead to venous thrombosis and pulmonary embolism.
GET
/api/v1/systems/nci_thesaurus/nodes/C98815Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.