Alpha thalassaemia (Q39515): Difference between revisions
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Latest revision as of 04:57, 13 August 2026
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A50.0 |
||
| English | Alpha thalassaemia |
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. |
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CID11:3A50.0
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dki-india-3A50.0
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Concluído
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13 August 2026
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