Haemolytic anaemias

D55 Anaemia due to enzyme disorders

• D55 Anaemia due to enzyme disorders
• D55.0 Anaemia due to glucoses-6-phosphate dehydrogenase [G6PD] deficiency
• D55.1 Anaemia due to other disorders of glutathione metabolism
• D55.2 Anaemia due to disorders of glycolytic enzymes
• D55.3 Anaemia due to disorders of nucleotide metabolism
• D55.8 Other anaemias due to enzyme disorders
• D55.9 Anaemia due to enzyme disorder, unspecified

D56 Thalassaemia

• D56 Thalassaemia
• D56.0 Alpha thalassaemia
• D56.1 Beta thalassaemia
• D56.2 Delta-beta thalassaemia
• D56.3 Thalassaemia trait
• D56.4 Hereditary perstence of fetal haemoglobin [HPFH]
• D56.8 Other thalassaemias
• D56.9 Thalassaemias, unspecified

D57 Sickle-cell disorders

• D57 Sickle-cell disorders
• D57.0 Sickle-cell anaemia with crisis
• D57.1 Sickle-cell anaemia without crisis
• D57.2 Double heterozygous sickling disorders
• D57.3 Sickle-cell trait
• D57.8 Other sickle-cell disorders

D58 Other hereditary haemolytic anaemias

• D58 Other hereditary haemolytic anaemias
• D58.0 Hereditary spherocytosis
• D58.1 Hereditary elliptocytosis
• D58.2 Other haemoglobinopathies
• D58.8 Other specified hereditary haemolytic anaemias
• D58.9 Hereditary haemolytic anaemia, unspecified

D59 Acquired haemolytic anaemia

• D59 Acquired haemolytic anaemia
• D59.0 Drug-induced autoimmune haemolytic anaemia
• D59.1 Other autoimmune haemolytic anaemias
• D59.2 Drug-induced nonautoimmune haemolytic anaemia
• D59.3 Haemolytic-uraemic syndrome
• D59.4 Other nonautoimmune haemolytic anaemia
• D59.5 Paraxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]
• D59.6 Haemoglobinuria due to haemolysis from other external causes
• D59.8 Other acquired haemolytic anaemias
• D59.9 Acquired haemolytic anaemia, unspecified