Alpha thalassaemia
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
Alpha-thalassemia is an inherited haemoglobinopathy characterised by impaired synthesis of alpha-globin chains leading to a variable clinical picture depending on the number of affected alleles, and encompassing the alpha thalassaemia trait, haemoglobin H disease (HbH) and Bart's hydrops fetalis.
exclusions
sections/codes in this section (3A50.0-3A50.0)
- Mild alpha thalassaemia diseases (3A50.00)
- Thalassaemic alpha-chain variants (3A50.01)
- Haemoglobin H disease (– α/– – included) (3A50.02)
- Homozygous or compound heterozygous alpha0 thalassaemia (3A50.03)
- Other specified alpha thalassaemia (3A50.0Y)
- Alpha thalassaemia, unspecified (3A50.0Z)
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com