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congenital nonspherocytic hemolytic anemia (DOID:2861)
Annotations: Rat: (13) Mouse: (13) Human: (14) Chinchilla: (12) Bonobo: (11) Dog: (13) Squirrel: (11) Pig: (12)
Parent Terms Term With Siblings Child Terms
congenital dyserythropoietic anemia +   
Congenital Hemolytic Anemia with Emphysema and Cutis Laxa 
congenital nonspherocytic hemolytic anemia +   
Any one of a group of congenital hemolytic anemias in which there is no abnormal hemoglobin or spherocytosis and in which there is a defect of glycolysis in the erythrocyte. Common causes include deficiencies in GLUCOSE-6-PHOSPHATE ISOMERASE; PYRUVATE KINASE; and GLUCOSE-6-PHOSPHATE DEHYDROGENASE.
Dehydrated Hereditary Stomatocytosis +   
glucosephosphate dehydrogenase deficiency +   
hemoglobin C disease  
hemoglobinopathy +   
hereditary elliptocytosis +   
hereditary spherocytosis +   
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: CNSHA ;   HNSHA ;   chronic nonspherocytic hemolytic anemia ;   hereditary nonspherocytic hemolytic anemia
Primary IDs: MESH:D000746 ;   RDO:0004830
Xrefs: ORDO:712
Definition Sources: MESH:D000746

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