Mild alpha thalassaemia diseases (Q39519): Difference between revisions
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Revision as of 04:58, 13 August 2026
A disease caused by genetically inherited factors affecting the alpha chain of the haemoglobin molecule. This disease is characterised by structural abnormalities of the haemoglobin molecule. This disease may present with mild anaemia: pallor, fatigue, shortness of breath. Confirmation is by identification of changes to the alpha chain by genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A50.00 |
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| English | Mild alpha thalassaemia diseases |
A disease caused by genetically inherited factors affecting the alpha chain of the haemoglobin molecule. This disease is characterised by structural abnormalities of the haemoglobin molecule. This disease may present with mild anaemia: pallor, fatigue, shortness of breath. Confirmation is by identification of changes to the alpha chain by genetic testing. |
