Congenital factor VII deficiency

Disease Export to PDF
Name:
Congenital factor VII deficiency
Description:
A rare, genetic, congenital vitamin K-dependant coagulation factor deficiency disorder characterized by decreased levels or absence of coagulation factor VII (FVII), resulting in bleeding diathesis of variable severity.
ORPHAcode:
327
Synonyms:
Congenital proconvertin deficiency
Hypoproconvertinemia
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14