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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
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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
Hereditary Hemorrhagic Telangiectasia
Medications / Treatment
Disorder Overview
Pattern of Inheritance
Clinical Manifestation
Differential Diagnosis
Management
Laboratory Evaluation
Medications / Treatment
Research
Resources
References