3A10.00 Haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2026-01
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
- Favism
- G6PD - [glucose-6-phosphate dehydrogenase deficiency] anaemia
- Haemolytic anaemia due toG6PD deficiency
- anaemia due to glucose-6-phosphate dehydrogenase deficiency
- anaemia due to pentose phosphate pathway defect
- favism anaemia
- glucose-6-phosphate dehydrogenase deficiency anaemia
- glucose-6-phosphate dehydrogenase deficiency with anaemia
- pentose phosphate pathway disorder anaemia
- Baghdad spring anaemia
- Hereditary haemolytic nonspherocytic type 1 anaemia
- anaemia due to haemolytic nonspherocytic (hereditary), type 1
- haemolytic nonspherocytic type 1 anaemia
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