Catalog
Haemolytic anaemias due to disorders of glycolytic enzymes
No MMS code
Link to WHO Definition
Haemolytic anaemias due to disorders of glycolytic enzymes – http://id.who.int/icd/entity/265398117
This is a form of anaemia due to haemolysis, the abnormal breakdown of red blood cells (RBCs), either in the blood vessels (intravascular haemolysis) or elsewhere in the human body (extravascular). This diagnosis is due to the metabolic pathway that converts glucose C6H12O6, into pyruvate, CH3COCOO- + H+.
Parents
Children
- Glycogen storage disease due to aldolase A deficiency
- Glycogen storage disease due to phosphoglycerate kinase 1 deficiency
- Haemolytic anaemia due to red cell enolase deficiency
- Nonspherocytic haemolytic anaemia due to hexokinase deficiency
- Glycogen storage disease due to muscle phosphofructokinase deficiency
- Haemolytic anaemia due to red cell diphosphoglycerate mutase deficiency
- Haemolytic anaemia due to red cell pyruvate kinase deficiency
- Haemolytic anaemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency
- Haemolytic anaemia due to triose phosphate-isomerase deficiency
- Haemolytic anaemia due to glucose-phosphate isomerase deficiency
- Haemolytic nonspherocytic hereditary anaemia, type 2