D55-D59
Haemolytic anaemias
- D55.0Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
- D55.1Anaemia due to other disorders of glutathione metabolism
- D55.2Anaemia due to disorders of glycolytic enzymes
- D55.3Anaemia due to disorders of nucleotide metabolism
- D55.8Other anaemias due to enzyme disorders
- D55.9Anaemia due to enzyme disorder, unspecified
- D56.0Alpha thalassaemia
- D56.1Beta thalassaemia
- D56.2Delta-beta thalassaemia
- D56.3Thalassaemia trait
- D56.4Hereditary persistence of fetal haemoglobin [HPFH]
- D56.8Other thalassaemias
- D56.9Thalassaemia, unspecified
- D57.0Sickle-cell anaemia with crisis
- D57.1Sickle-cell anaemia without crisis
- D57.2Double heterozygous sickling disorders
- D57.3Sickle-cell trait
- D57.8Other sickle-cell disorders
- D58.0Hereditary spherocytosis
- D58.1Hereditary elliptocytosis
- D58.2Other haemoglobinopathies
- D58.8Other specified hereditary haemolytic anaemias
- D58.9Hereditary haemolytic anaemia, unspecified
- D59.0Drug-induced autoimmune haemolytic anaemia
- D59.1Other autoimmune haemolytic anaemias
- D59.2Drug-induced nonautoimmune haemolytic anaemia
- D59.3Haemolytic-uraemic syndrome
- D59.4Other nonautoimmune haemolytic anaemias
- D59.5Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]
- D59.6Haemoglobinuria due to haemolysis from other external causes
- D59.8Other acquired haemolytic anaemias
- D59.9Acquired haemolytic anaemia, unspecified