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Ontology Browser

Parent Terms Term With Siblings Child Terms
Activated Protein C Resistance  
alpha-2-plasmin inhibitor deficiency  
antithrombin III deficiency  
Bernard-Soulier syndrome +   
blood platelet disease +   
Chondrodysplasia Punctata with Coagulation Factor Deficiency 
congenital afibrinogenemia +   
Congenital Plasminogen Deficiency 
disseminated intravascular coagulation +   
Dysfibrinogenemia Causing Recurrent Thrombosis 
Essential Athrombia 
essential thrombocythemia  
factor V deficiency +   
A deficiency of blood coagulation factor V (known as proaccelerin or accelerator globulin or labile factor) leading to a rare hemorrhagic tendency known as Owren's disease or parahemophilia. It varies greatly in severity. Factor V deficiency is an autosomal recessive trait. (Dorland, 27th ed)
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 Hemorrhagic Diathesis due to Antithrombin 
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  
Flood Factor Deficiency 
Glanzmann's thrombasthenia +   
gray platelet syndrome +   
hemophilia B  
Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts  
Hermansky-Pudlak syndrome +   
Passovoy Factor 
Pechet Factor Deficiency 
Plasminogen Activator Inhibitor-1 Deficiency  
platelet 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 16  
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 +   
Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency  
purpura +   
Quebec platelet disorder  
Scott syndrome  
Tatsumi Factor Deficiency 
vascular hemostatic disease +   
vitamin K deficiency bleeding  
Vitamin K-Dependent Clotting Factors, Combined Deficiency Of, 1  
Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2  
von Willebrand's disease +   
Waterhouse-Friderichsen syndrome +  
Wiskott-Aldrich syndrome +   

Exact Synonyms: Factor V Deficiencies ;   Hereditary hypoproaccelerinaemia ;   Labile Factor Deficiencies ;   Labile Factor Deficiency ;   Owren Disease ;   Owren Parahemophilia ;   Owren's Disease ;   Owrens Disease ;   Parahemophilia ;   Parahemophilias ;   Proaccelerin deficiency ;   deficiency, labile
Primary IDs: MESH:D005166 ;   RDO:0001767
Alternate IDs: OMIM:227400
Xrefs: GARD:2237 ;   NCI:C98938
Definition Sources: MESH:D005166

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