Skip to content
Home
About
Disorders
Rare Congenital Disorders of Fibrinogen
Prothrombin (Factor II) Deficiency
Plasminogen Deficiency
Plasminogen Activator Inhibitor Type 1 Deficiency
Factor V Deficiency
Combined FV and FVIII Deficiency
Congenital Platelet Function Disorders
Alpha 2-Antiplasmin Deficiency
Factor VII Deficiency
Factor X Deficiency
Hereditary Hemorrhagic Telangiectasia
Factor XI Deficiency
FXIII Deficiency
Congenital Deficiency of Vitamin K-Dependent Clotting Factors
Authors
Resources
Menu
Home
About
Disorders
Rare Congenital Disorders of Fibrinogen
Prothrombin (Factor II) Deficiency
Plasminogen Deficiency
Plasminogen Activator Inhibitor Type 1 Deficiency
Factor V Deficiency
Combined FV and FVIII Deficiency
Congenital Platelet Function Disorders
Alpha 2-Antiplasmin Deficiency
Factor VII Deficiency
Factor X Deficiency
Hereditary Hemorrhagic Telangiectasia
Factor XI Deficiency
FXIII Deficiency
Congenital Deficiency of Vitamin K-Dependent Clotting Factors
Authors
Resources
Contact
Congenital Deficiency of Vitamin K-Dependent Clotting Factors
Research
Researchers with a special interest in the area of
VKCFD
:
Source:
www.orpha.net
Disorder Overview
Pattern of Inheritance
Clinical Manifestation
Differential Diagnosis
Laboratory Evaluation
Medications / Treatment
Research
Resources
References