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Congenital factor V deficiency
What is Congenital factor V deficiency?
Congenital factor V deficiency is an inherited bleeding disorder due to reduced plasma levels of factor V (FV) and characterized by mild to severe bleeding symptoms.
Other condition names
Owren disease
Parahemophilia
Proaccelerin deficiency
Inheritance type
Autosomal recessive
Prevalence
Europe: 1-9 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.