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3A10.00 Haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

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.

synonyms

• Haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency
• Chronic non spherocytic anaemia
• G6PD - [glucose-6-phosphate dehydrogenase deficiency] anaemia
• anaemia due to glucose-6-phosphate dehydrogenase deficiency
• glucose-6-phosphate dehydrogenase deficiency with anaemia
• glucose-6-phosphate dehydrogenase deficiency anaemia
• favism anaemia
• Haemolytic anaemia due toG6PD deficiency
• Favism
• pentose phosphate pathway disorder anaemia
• anaemia due to pentose phosphate pathway defect
• Baghdad spring anaemia
• Hereditary haemolytic nonspherocytic type 1 anaemia
• haemolytic nonspherocytic type 1 anaemia
• anaemia due to haemolytic nonspherocytic (hereditary), type 1

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