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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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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
Plasminogen Deficiency
Resources
Patient resources
Rare Diseases International (RDI)
https://www.rarediseasesinternational.org/
https://www.rarediseasesinternational.org/members-list/
(This page contains the list for international alliance of rare disorders websites)
National Organization for Rare Disorders (NORD)
203-744-0100
https://rarediseases.org/
https://rarediseases.org/contact-us/
(This page contains the links for US national rare disease organizations)
Genetic Alliance
202.966.5557
http://www.geneticalliance.org
info@geneticalliance.org
Genetics Home Reference (U.S. National Library of Medicine)
https://ghr.nlm.nih.gov/
Disorder Overview
Pattern of Inheritance
Clinical Manifestation
Differential Diagnosis
Laboratory Evaluation
Medications / Treatment
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References