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Ontology Browser
Term:
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 +   
hemoglobinopathy +   
hereditary elliptocytosis +   
A hematopoietic system disease characterized by oval or elliptical red blood cells, slight or absent hemolysis with little or no anemia; splenomegaly is often present. (DO)
hereditary spherocytosis +   
Nonspherocytic Hemolytic Anemia due to Glucose Phosphate Isomerase Deficiency  
overhydrated hereditary stomatocytosis  
Red Cell Phospholipid Defect with Hemolysis 
Rh-Null Disease, Amorph Type  
sickle cell anemia +   
Stomatocytosis II  
Transient Erythroblastopenia of Childhood 
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to  
X-linked congenital hemolytic anemia  

Synonyms
Exact Synonyms: Hereditary Elliptocytoses ;   Hereditary Ovalocytoses ;   Hereditary Ovalocytosis ;   congenital elliptocytosis ;   hereditary stomatocytic elliptocytosis ;   ovalocytosis
Broad Synonyms: ELLIPTOCYTOSIS
Primary IDs: MESH:D004612
Xrefs: GARD:6621 ;   ICD10CM:D58.1 ;   ICD9CM:282.1 ;   NCI:C35882 ;   ORDO:288
Definition Sources: http://en.wikipedia.org/wiki/Hereditary_elliptocytosis "DO" "DO", http://www.merckmanuals.com/professional/hematology_and_oncology/anemias_caused_by_hemolysis/hereditary_spherocytosis_and_hereditary_elliptocytosis.html "DO" "DO", https://research.nhgri.nih.gov/RBCmembrane/ "DO" "DO"

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