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Ontology Browser

Parent Terms Term With Siblings Child Terms
thrombophilia +     
agammaglobulinemia +   
Antithrombin Deficiency Type 2 
antithrombin III deficiency  
Corticosteroid-Binding Globulin, Elevated 
Deficiency of Plasma Clot Retraction Factor 
disseminated intravascular coagulation +   
dysgammaglobulinemia +   
Factor V Excess with Spontaneous Thrombosis 
Familial Thrombomodulin Anomalies 
heparin cofactor II deficiency  
Hereditary Thrombophilia  
Hypergammaglobulinemia +   
Hypoglobulinemia and Absent B Cells 
Hypoproteinemia +   
Kininogen Deficiency, High Molecular Weight and Low Molecular Weight  
Paraproteinemias +   
protein C deficiency +   
protein S deficiency +   
A thrombophilia that is characterized by increased risk of developing abnormal blood clots. (DO)
prothrombin deficiency +   
prothrombin thrombophilia 
sickle cell anemia +   
sulfhemoglobinemia +  
thrombophilia due to activated protein C resistance  
thrombophilia due to decreased release of PLAT  
thrombophilia due to HRG deficiency  
thrombophilia due to thrombin defect  
thrombophilia due to thrombomodulin defect  
thrombotic thrombocytopenic purpura +   
X-linked thrombophilia due to factor IX defect  
X-Linked Thrombophilia due to Factor VIII Defect  

Exact Synonyms: Hereditary Thrombophilia Due To Protein S Deficiency ;   protein S deficiencies ;   protein S deficiency disease
Primary IDs: MESH:D018455
Xrefs: GARD:4524 ;   NCI:C99026
Definition Sources: "DO" "DO"

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