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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.