congenital nonspherocytic hemolytic anemia
MONDO:0006506Mondo
Findings
No curated finding names congenital nonspherocytic hemolytic anemia yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0006506), read 2026-09-29. CC BY 4.0.
Where it sits
- Narrower terms (10)
- anemia, nonspherocytic hemolytic
- 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
Other names
2 names
Resolves to: congenital nonspherocytic hemolytic anemia
- Also called
- anemia, congenital, nonspherocytic hemolyticHereditary nonspherocytic hemolytic anemia