Congenital plasminogen activator inhibitor type 1 deficiency

Disease Export to PDF
Name:
Congenital plasminogen activator inhibitor type 1 deficiency
Description:
A rare hemorrhagic disorder due to a constitutional haemostatic factors defect characterized by premature lysis of hemostatic clots and a moderate bleeding tendency.
ORPHAcode:
465
Synonyms:
Congenital PAI-1 deficiency
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14