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Ontology Browser

Parent Terms Term With Siblings Child Terms
anemia +     
anemia +   
Autosomal Dominant Tubulointerstitial Kidney Disease 4  
blood coagulation disease +   
blood group incompatibility +   
blood protein disease +   
bone marrow disease +   
Congenital Dyserythropoiesis with Internuclear Chromatin Bridges and Ultrastructurally Normal Erythroblast Heterochromatin 
Drug-induced Anemia  
Elevated Adenosine Triphosphate of Erythrocytes  
Familial Macrocytosis  
folic acid deficiency anemia +   
Hematologic Neoplasms +   
Hematologic Pregnancy Complications 
hypochromic anemia +   
Kabuki syndrome +   
leukocyte disease +   
macrocytic anemia +   
Malarial Anemia  
microcytic anemia +   
Mosaic Variegated Aneuploidy Syndrome 5  
neonatal anemia +   
normocytic anemia +   
pancytopenia +   
An anemia that is characterized by a reduction in the number of red blood cells, white blood cells, and platelets. (DO)
polyagglutination +   
polycythemia +   
protein-deficiency anemia 
pyridoxine deficiency anemia  
Refractory Anemia +   
Rh isoimmunization  
sulfhemoglobinemia +  
Thrombocytopenia, Anemia, and Myelofibrosis  
Tn polyagglutination syndrome  
Transfusion Reaction +   
X-Linked Anemia without Thrombocytopenia 
X-linked dyserythropoietic anemia  

Exact Synonyms: pancytopenias
Primary IDs: MESH:D010198
Xrefs: ICD10CM:D61.81 ;   ICD9CM:284.1 ;   NCI:C34889 ;   NCI:C80693
Definition Sources: "DO" "DO"

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