Catalog
Other haemoglobinopathies
No MMS code
Link to WHO Definition
Other haemoglobinopathies – http://id.who.int/icd/entity/1546263654
Any disease caused by determinants leading to abnormalities the integral structure of the haemoglobin molecule. This disease is characterised by decreased levels of red blood cells in the body. Confirmation is by identification of decreased red blood cell count in a blood sample.
Parents
Children
- Haemoglobin C trait
- 3A51.8 Low affinity haemoglobin
- Acquired haemoglobin H in myelodysplastic disorders
- 3A51.7 High affinity haemoglobin
- 3A51.9 Haemoglobin O disease
- 3A51.6 Haemoglobin D disease
- Compound HbC or beta thalassaemia heterozygotes
- Unstable haemoglobin haemolytic disease
- 3A51.B Haemoglobin C/beta thalassaemia compound heterozygosity
- Compound HbE beta thalassaemia heterozygotes
- 3A51.A Haemoglobin E disease
- Haemoglobin E trait
- 3A51.5 Haemoglobin C disease
- FB81.4 Osteonecrosis due to haemoglobinopathy
- Stransky-Regala type haemolytic anaemia
- Haemoglobin C A disorder