Haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency (Q39506): Difference between revisions
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13 August 2026
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Revision as of 04:57, 13 August 2026
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common hereditary erythrocyte enzyme deficiency that can manifest with severe neonatal jaundice which can lead to serious neurological consequences, or, most often, with acute haemolytic anaemia following ingestion of certain foods (fava beans), common drugs (some antimalaria drugs, sulphamides, analgesics), or in the course of an infection, in otherwise asymptomatic individuals.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A10.00 |
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| English | Haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency |
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common hereditary erythrocyte enzyme deficiency that can manifest with severe neonatal jaundice which can lead to serious neurological consequences, or, most often, with acute haemolytic anaemia following ingestion of certain foods (fava beans), common drugs (some antimalaria drugs, sulphamides, analgesics), or in the course of an infection, in otherwise asymptomatic individuals. |
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CID11:3A10.00
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dki-india-3A10.00
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Concluído
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13 August 2026
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