Congenital factor II deficiency
What is Congenital factor II deficiency?
A rare inherited bleeding disorder due to reduced activity of factor II (FII, prothrombin) and characterized by mucocutaneous and soft tissue 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.