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Ontology Browser

Parent Terms Term With Siblings Child Terms
acquired von Willebrand syndrome 
anemia +   
Bleeding Disorder, East Texas Type 
blood coagulation disease +   
blood group incompatibility +   
blood protein disease +   
bone marrow disease +   
Car Factor Deficiency 
Coagulation Protein Disorders +   
Deficiency of Plasma Clot Retraction Factor 
disseminated intravascular coagulation +   
Elevated Adenosine Triphosphate of Erythrocytes  
Familial Macrocytosis  
fetal erythroblastosis +   
Fibrinolytic Defect 
Globulin Anomaly involving Beta (2A)-Globulin 
Hematologic Neoplasms +   
Hematologic Pregnancy Complications 
hemorrhagic disease +   
Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (BLOOD COAGULATION DISORDERS) or another abnormality causing a structural flaw in the blood vessels (HEMOSTATIC DISORDERS).
hereditary elliptocytosis +   
Inherited Blood Coagulation Disease +   
Kabuki syndrome +   
leukocyte disease +   
pancytopenia +   
platelet storage pool deficiency +   
Platelet-Type Bleeding Disorder 13  
polycythemia +   
Prekallikrein Deficiency  
purpura +   
Rh isoimmunization  
sulfhemoglobinemia +  
thrombophilia +   
Tn polyagglutination syndrome  
Transfusion Reaction 
vitamin D-dependent rickets +   

Exact Synonyms: Hemorrhagic Diatheses ;   Hemorrhagic Diathesis ;   Hemorrhagic Disorder ;   Hemorrhagic Disorders
Primary IDs: MESH:D006474 ;   RDO:0003677
Xrefs: ICD10CM:D69.9 ;   ICD9CM:287.9
Definition Sources: MESH:D006474

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