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Ontology Browser
Term:
congenital nonspherocytic hemolytic anemia (EFO:1000641)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0) Naked Mole-rat: (0) Green Monkey: (0)
Parent Terms Term With Siblings Child Terms
abetalipoproteinemia 
Autosomal dominant methemoglobinemia 
beta-thalassemia and related diseases +  
congenital dyserythropoietic anemia +  
congenital dyserythropoietic anemia type 1 
congenital dyserythropoietic anemia type 2 
congenital dyserythropoietic anemia type 3 
congenital dyserythropoietic anemia type 4 
Congenital dyserythropoietic anemia type I 
Congenital dyserythropoietic anemia type II 
Congenital dyserythropoietic anemia type III 
Congenital dyserythropoietic anemia type IV 
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.
Constitutional deficiency anemia +  
Constitutional sideroblastic anemia +  
cryohydrocytosis 
cutaneous porphyria 
dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema 
elliptocytosis 2 
familial pseudohyperkalemia 
Fanconi anemia +  
glycogen storage disease due to aldolase A deficiency 
glycogen storage disease VII 
hemoglobin C disease 
hemoglobin D disease 
hemoglobin E disease  
Hemoglobin SC Disease 
hemoglobinopathy Toms River 
hemolytic anemia due to adenylate kinase deficiency 
hemolytic anemia due to diphosphoglycerate mutase deficiency 
hemolytic anemia due to erythrocyte adenosine deaminase overproduction 
hemolytic anemia due to glutathione reductase deficiency 
hemolytic anemia due to pyrimidine 5' nucleotidase deficiency 
hereditary cryohydrocytosis with reduced stomatin 
hereditary methemoglobinemia +  
hereditary persistence of fetal hemoglobin-sickle cell disease syndrome 
hereditary spherocytosis +  
myopathy, lactic acidosis, and sideroblastic anemia 
non-spherocytic hemolytic anemia due to hexokinase deficiency 
overhydrated hereditary stomatocytosis 
Pancreatic insufficiency - anemia - hyperostosis 
primary CD59 deficiency 
Rare constitutional hemolytic anemia +  
Recessive hereditary methemoglobinemia type 1 
Recessive hereditary methemoglobinemia type 2 
renal tubular acidosis, distal, 4, with hemolytic anemia 
Rh deficiency syndrome 
severe congenital hypochromic anemia with ringed sideroblasts 
Sickle cell - beta-thalassemia disease 
Sickle cell - hemoglobin C disease 
Sickle cell - hemoglobin D disease 
Sickle cell - hemoglobin E disease 
sickle cell anemia +   
sickle cell disease and related diseases 
sickle cell-beta-thalassemia disease syndrome 
sickle cell-hemoglobin d disease syndrome 
sickle cell-hemoglobin E disease syndrome 
southeast Asian ovalocytosis 
Thalassemia +  
triosephosphate isomerase deficiency 

Synonyms
Exact Synonyms: HNSHA ;   hereditary nonspherocytic hemolytic anaemia ;   hereditary nonspherocytic hemolytic anemia
Xrefs: DOID:2861 ;   ICD9:282.3 ;   MEDGEN:284 ;   MESH:D000746 ;   MONDO:0006506 ;   SCTID:301317008 ;   UMLS:C0002882
Definition Sources: MESH:D000746

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