Congenital nonspherocytic hemolytic anemia
MONDO:0006506Any 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
63 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Pyruvate kinase deficiency of red cells
(10)
Anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane
(1)
Anemia, nonspherocytic hemolytic, due to G6PD deficiency
(1)
Hemolytic anemia due to adenylate kinase deficiency
(1)
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency
(1)
Anemia, nonspherocytic hemolytic
(0)
Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism
(0)
Gamma-glutamylcysteine synthetase deficiency
(0)
Glutathione synthetase deficiency without 5-oxoprolinuria
(0)
Hemolytic anemia due to erythrocyte adenosine deaminase overproduction
(0)
Hemolytic anemia due to glucophosphate isomerase deficiency
(0)
Hemolytic anemia due to glutathione reductase deficiency
(0)
Non-spherocytic hemolytic anemia due to hexokinase deficiency
(0)