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Ontology Browser

Parent Terms Term With Siblings Child Terms
congenital dyserythropoietic anemia +   
Congenital Hemolytic Anemia with Emphysema and Cutis Laxa 
congenital nonspherocytic hemolytic anemia +   
Dehydrated Hereditary Stomatocytosis +   
glucosephosphate dehydrogenase deficiency +   
Heinz Body Anemias  
hemoglobin C disease  
hemoglobinopathy +   
A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
hereditary elliptocytosis +   
hereditary spherocytosis +   
Lethal Congenital Nonspherocytic Hemolytic Anemia with Genital and Other Abnormalities 
Nonspherocytic Hemolytic Anemia due to Glucose Phosphate Isomerase Deficiency  
Red Cell Phospholipid Defect with Hemolysis 
Rh-Null Disease, Amorph Type  
sickle cell anemia +   
Stomatocytosis I  
Stomatocytosis II  
thalassemia +   
Transient Erythroblastopenia of Childhood 
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to  

Exact Synonyms: hemoglobinopathies
Related Synonyms: Hb Footscray ;   Hemoglobin Adana ;   Hemoglobin Aghia Sophia ;   Hemoglobin Agrinio ;   Hemoglobin Clinico-Madrid ;   Hemoglobin Footscray ;   Hemoglobin Icaria ;   Hemoglobin Sallanches ;   abnormal hemoglobin ;   hemoglobin Val de Marne
Primary IDs: MESH:D006453
Alternate IDs: RDO:0004839
Xrefs: GARD:12455 ;   NCI:C3092
Definition Sources: MESH:D006453

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