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Up to: Inherited hemoglobinopathy · Congenital anemia · Familial hemolytic anemia

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.

1 trial tagged with this condition →

Pyruvate kinase deficiency of red cells 10 trials
Anemia, nonspherocytic hemolytic 0 trials · 2 incl. sub-types Sub-types →
Hemolytic anemia due to adenylate kinase deficiency 1 trial
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency 1 trial
Gamma-glutamylcysteine synthetase deficiency 0 trials
Glutathione synthetase deficiency without 5-oxoprolinuria 0 trials
Hemolytic anemia due to erythrocyte adenosine deaminase overproduction 0 trials
Hemolytic anemia due to glucophosphate isomerase deficiency 0 trials
Hemolytic anemia due to glutathione reductase deficiency 0 trials
Non-spherocytic hemolytic anemia due to hexokinase deficiency 0 trials