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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
antithrombin III deficiency  
autosomal hemophilia A 
Bernard-Soulier syndrome +   
Chediak-Higashi syndrome +   
congenital afibrinogenemia +   
Dysprothrombinemia 
Essential Athrombia 
factor V deficiency +   
factor VII deficiency  
factor VIII deficiency +   
factor X deficiency  
factor XI deficiency  
factor XII deficiency  
factor XIII deficiency +   
Factors VIII, IX and XI, Combined Deficiency of 
Familial Multiple Coagulation Factor Deficiency II 
Familial Multiple Coagulation Factor Deficiency IV 
Familial Multiple Coagulation Factor Deficiency VI 
Familial Platelet Disorder with Associated Myeloid Malignancy  
Glanzmann's thrombasthenia +   
gray platelet syndrome +   
hemophilia B  
Hermansky-Pudlak syndrome +   
A syndrome characterized by oculocutaneous albinism, bleeding problems due to platelet storage pool defect, visual impairment and lysosomal accumulation of ceroid lipofuscin. (DO)
high molecular weight kininogen deficiency  
Passovoy Factor 
Pechet Factor Deficiency 
Platelet Alpha/Delta Storage Pool Deficiency 
platelet-type bleeding disorder 10  
platelet-type bleeding disorder 11  
platelet-type bleeding disorder 12 
platelet-type bleeding disorder 14  
platelet-type bleeding disorder 15  
platelet-type bleeding disorder 17  
platelet-type bleeding disorder 18  
platelet-type bleeding disorder 19  
platelet-type bleeding disorder 20  
platelet-type bleeding disorder 3  
platelet-type bleeding disorder 8  
platelet-type bleeding disorder 9  
Prolonged Bleeding Time, Brachydactyly, and Mental Retardation  
protein C deficiency +   
prothrombin deficiency +   
Scott syndrome  
thrombophilia due to activated protein C resistance  
Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1  
Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2  
von Willebrand's disease +   
Wiskott-Aldrich syndrome +   

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.