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Congenital nonspherocytic hemolytic anemia

MONDO:0006506

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.

Also known as: anemia, congenital, nonspherocytic hemolytic

34 clinical trials for this condition and its sub-types, 1 tagged with Congenital nonspherocytic hemolytic anemia itself.

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