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hereditary elliptocytosis (DOID:2373)
Annotations: Rat: (9) Mouse: (9) Human: (9) Chinchilla: (8) Bonobo: (9) Dog: (9) Squirrel: (9) Pig: (9)
Parent Terms Term With Siblings Child Terms
anemia +   
blood coagulation disease +   
blood group incompatibility +   
blood protein disease +   
bone marrow disease +   
congenital dyserythropoietic anemia +   
Congenital Hemolytic Anemia with Emphysema and Cutis Laxa 
congenital nonspherocytic hemolytic anemia +   
dehydrated hereditary stomatocytosis +   
Elevated Adenosine Triphosphate of Erythrocytes  
Familial Macrocytosis  
fetal erythroblastosis +   
glucosephosphate dehydrogenase deficiency +   
Hematologic Neoplasms +   
hemoglobinopathy +   
hemorrhagic disease +   
hereditary elliptocytosis +   
An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.
hereditary spherocytosis +   
Kabuki syndrome +   
leukocyte disease +   
Nonspherocytic Hemolytic Anemia due to Glucose Phosphate Isomerase Deficiency  
overhydrated hereditary stomatocytosis  
pancytopenia +   
polycythemia +   
Pregnancy Complications, Hematologic 
Red Cell Phospholipid Defect with Hemolysis 
Rh isoimmunization  
Rh-Null Disease, Amorph Type  
sickle cell anemia +   
Stomatocytosis II  
sulfhemoglobinemia +  
thalassemia +   
Tn polyagglutination syndrome  
Transfusion Reaction 
Transient Erythroblastopenia of Childhood 
Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia due to  
X-linked congenital hemolytic anemia  

Exact Synonyms: Hereditary Elliptocytoses ;   Hereditary Ovalocytoses ;   Hereditary Ovalocytosis ;   Stomatocytic Elliptocytosis, Hereditary ;   congenital elliptocytosis ;   ovalocytosis
Primary IDs: MESH:D004612
Alternate IDs: RDO:0005452
Xrefs: GARD:6621 ;   ICD10CM:D58.1 ;   ICD9CM:282.1 ;   NCI:C35882 ;   ORDO:288
Definition Sources: "DO", "DO", MESH:D004612

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