ORPHA:82
Hereditary thrombophilia due to congenital antithrombin deficiency
Also called Hereditary thrombophilia due to congenital antithrombin 3 deficiency
- Body system
- Bone diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Adolescent, Adult
- Estimated prevalence
- 1-5 / 10 000 (Worldwide)
- Rarity class
- 1-5 / 10 000
ORPHA:82 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Reduced antithrombin III activity
- Reduced antithrombin antigen
- Pulmonary embolism
- Deep venous thrombosis
- Superficial thrombophlebitis
- Recurrent thromboembolism