Congenital factor V deficiency

Disease Export to PDF
Name:
Congenital factor V deficiency
Description:
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.
ORPHAcode:
326
Synonyms:
Owren disease
Parahemophilia
Proaccelerin deficiency
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14