Congenital factor II deficiency
What is Congenital factor II deficiency?
An inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous bleeding symptoms.
Other condition names
- Dysprothrombinemia
- Hypoprothrombinemia
- Prothrombin deficiency
Inheritance type
Autosomal recessive
Prevalence
- Europe: <1 in 1,000 000
Age of Onset
- All ages
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.