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Congenital factor V deficiency

rare

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.

Identifiers
MONDO:0009210 OMIM:227400Orphanet:326
Causal genes
F5
Part of
Factor V deficiencyHemorrhagic diseaseInherited blood coagulation disorder
Also known as
hereditary Factor V deficiency · labile factor deficiency · Owren disease · Parahemophilia · Proaccelerin deficiency

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