Congenital factor VII deficiency
MONDO:0009211Factor VII (FVII) deficiency is a rare hereditary hemorrhagic disease caused by the diminution or absence of this coagulation factor.
Also known as: congenital factor VII deficiency, congenital proconvertin deficiency, hypoproconvertinemia, F7 deficiency, factor 7 deficiency, factor VII deficiency
48 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trials