Chapter III
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
(D50-D89)
Haemolytic anaemias
(D55-D59)
| D55 | Anaemia due to enzyme disorders Latin: Anaemia haemolytica enzymopathica | |||||||
| Excludes: | drug-induced enzyme deficiency anaemia (D59.2) | |||||||
| D55.0 | Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency | |||||||
| Favism G6PD deficiency anaemia | ||||||||
| D55.1 | Anaemia due to other disorders of glutathione metabolism | |||||||
| Anaemia (due to): · enzyme deficiencies, except G6PD, related to the hexose monophosphate [HMP] shunt pathway · haemolytic nonspherocytic (hereditary), type I | ||||||||
| D55.2 | Anaemia due to disorders of glycolytic enzymes | |||||||
| Anaemia: · haemolytic nonspherocytic (hereditary), type II · hexokinase deficiency · pyruvate kinase [PK] deficiency · triose-phosphate isomerase deficiency | ||||||||
| 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 Latin: Thalassanaemia | |||||||
| D56.0 | Alpha thalassaemia | |||||||
| Excludes: | hydrops fetalis due to haemolytic disease (P56.-) | |||||||
| D56.1 | Beta thalassaemia | |||||||
| Cooley's anaemia Severe beta thalassaemia Thalassaemia: · intermedia · major | ||||||||
| D56.2 | Delta-beta thalassaemia | |||||||
| D56.3 | Thalassaemia trait | |||||||
| D56.4 | Hereditary persistence of fetal haemoglobin [HPFH] | |||||||
| D56.8 | Other thalassaemias | |||||||
| D56.9 | Thalassaemia, unspecified | |||||||
| Mediterranean anaemia (with other haemoglobinopathy) Thalassaemia (minor)(mixed)(with other haemoglobinopathy) | ||||||||
| D57 | Sickle-cell disorders Latin: Drepanocytosis | |||||||
| Excludes: | other haemoglobinopathies (D58.-) | |||||||
| D57.0 | Sickle-cell anaemia with crisis | |||||||
| Hb-SS disease with crisis | ||||||||
| D57.1 | Sickle-cell anaemia without crisis | |||||||
| Sickle-cell: | ||||||||
| · anaemia · disease · disorder | } } } | NOS | ||||||
| D57.2 | Double heterozygous sickling disorders | |||||||
| Disease: · Hb-SC · Hb-SD · Hb-SE · sickle-cell thalassaemia | ||||||||
| D57.3 | Sickle-cell trait | |||||||
| Hb-S trait Heterozygous haemoglobin S | ||||||||
| D57.8 | Other sickle-cell disorders | |||||||
| D58 | Other hereditary haemolytic anaemias Latin: Anaemiae haemolyticae hereditariae aliae | |||||||
| D58.0 | Hereditary spherocytosis | |||||||
| Acholuric (familial) jaundice Congenital (spherocytic) haemolytic icterus Minkowski-Chauffard syndrome | ||||||||
| D58.1 | Hereditary elliptocytosis | |||||||
| Elliptocytosis (congenital) Ovalocytosis (congenital)(hereditary) | ||||||||
| D58.2 | Other haemoglobinopathies | |||||||
| Abnormal haemoglobin NOS Congenital Heinz body anaemia Disease: · Hb-C · Hb-D · Hb-E Haemoglobinopathy NOS Unstable haemoglobin haemolytic disease | ||||||||
| Excludes: | familial polycythaemia (D75.0) Hb-M disease (D74.0) hereditary persistence of fetal haemoglobin [HPFH] (D56.4) high-altitude polycythaemia (D75.1) methaemoglobinaemia (D74.-) | |||||||
| D58.8 | Other specified hereditary haemolytic anaemias | |||||||
| Stomatocytosis | ||||||||
| D58.9 | Hereditary haemolytic anaemia, unspecified | |||||||
| D59 | Acquired haemolytic anaemia Latin: Anaemia haemolytica acquisita | |||||||
| D59.0 | Drug-induced autoimmune haemolytic anaemia | |||||||
| Use additional external cause code (Chapter XX), if desired, to identify drug. | ||||||||
| D59.1 | Other autoimmune haemolytic anaemias | |||||||
| Autoimmune haemolytic disease (cold type)(warm type) Chronic cold haemagglutinin disease Cold agglutinin: · disease · haemoglobinuria Haemolytic anaemia: · cold type (secondary)(symptomatic) · warm type (secondary)(symptomatic) | ||||||||
| Excludes: | Evans' syndrome (D69.3) haemolytic disease of fetus and newborn (P55.-) paroxysmal cold haemoglobinuria (D59.6) | |||||||
| D59.2 | Drug-induced nonautoimmune haemolytic anaemia | |||||||
| Drug-induced enzyme deficiency anaemia | ||||||||
| Use additional external cause code (Chapter XX), if desired, to identify drug. | ||||||||
| D59.3 | Haemolytic-uraemic syndrome | |||||||
| D59.4 | Other nonautoimmune haemolytic anaemias | |||||||
| Haemolytic anaemia: · mechanical · microangiopathic · toxic | ||||||||
| Use additional external cause code (Chapter XX), if desired, to identify cause. | ||||||||
| D59.5 | Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli] | |||||||
| Excludes: | haemoglobinuria NOS (R82.3) | |||||||
| D59.6 | Haemoglobinuria due to haemolysis from other external causes | |||||||
| Haemoglobinuria: · from exertion · march · paroxysmal cold | ||||||||
| Use additional external cause code (Chapter XX), if desired, to identify cause. | ||||||||
| Excludes: | haemoglobinuria NOS (R82.3) | |||||||
| D59.8 | Other acquired haemolytic anaemias | |||||||
| D59.9 | Acquired haemolytic anaemia, unspecified | |||||||
| Idiopathic haemolytic anaemia, chronic | ||||||||
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