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


  • Europe: 1-9 in 1,000 000

Age of Onset

  • All ages
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