Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
ACANTHOCYTOSIS  
acquired von Willebrand syndrome 
Adenosine Triphosphate, Elevated, of Erythrocytes  
anemia +   
Bleeding Disorder, East Texas Type 
blood coagulation disease +   
blood group incompatibility +   
blood protein disease +   
bone marrow disease +   
Car Factor Deficiency 
coagulation protein disease +   
disseminated intravascular coagulation +   
Ecchymosis 
essential thrombocythemia  
Familial Macrocytosis  
fetal erythroblastosis +   
Fibrinolytic Defect 
Flaujeac Factor Deficiency  
Globulin Anomaly involving Beta (2A)-Globulin 
Hematologic Neoplasms +   
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 +   
Hyperheparinemia 
inherited blood coagulation disease +   
Kabuki syndrome +   
leukocyte disease +   
methemoglobinemia +   
pancytopenia +   
Plasma Clot Retraction Factor, Deficiency of 
platelet storage pool deficiency +   
Platelet-Type Bleeding Disorder 13  
platelet-type bleeding disorder 14  
polycythemia +   
Pregnancy Complications, Hematologic 
Prekallikrein Deficiency  
Preleukemias 
protein S deficiency +   
purpura +   
Rh deficiency syndrome  
Rh isoimmunization  
sulfhemoglobinemia +  
thrombophilia +   
Transfusion Reaction  

Synonyms
Exact Synonyms: Hemorrhagic Diatheses ;   Hemorrhagic Diathesis ;   Hemorrhagic Disorder ;   Hemorrhagic Disorders
Primary IDs: MESH:D006474 ;   RDO:0003677
Definition Sources: MESH:D006474

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