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Congenital nonspherocytic hemolytic anemia

rare

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.

Identifiers
MONDO:0006506
Part of
Congenital anemiaFamilial hemolytic anemiaInherited hemoglobinopathy
Also known as
anemia, congenital, nonspherocytic hemolytic · Hereditary nonspherocytic hemolytic anemia

Subtypes

All diseases Rare only
Disease Subtypes
Anemia, nonspherocytic hemolytic 3
Gamma-glutamylcysteine synthetase deficiency
Glutathione synthetase deficiency without 5-oxoprolinuria
Hemolytic anemia due to adenylate kinase deficiency
Hemolytic anemia due to erythrocyte adenosine deaminase overproduction
Hemolytic anemia due to glucophosphate isomerase deficiency
Hemolytic anemia due to glutathione reductase deficiency
Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency
Non-spherocytic hemolytic anemia due to hexokinase deficiency
Pyruvate kinase deficiency of red cells

Rare disease

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