Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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(D50–D89) Diseases Of The Blood And Blood-Forming Organs And Certain Disorders Involving The Immune Mechanism |
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D50–D53 |
Nutritional anemias |
|
D55–D59 |
Haemolytic anaemias |
|
D60–D64 |
Aplastic and other anaemias |
|
D65–D69 |
Coagulation defects, purpura and other haemorrhagic conditions |
|
D70–D77 |
Other diseases of blood and blood-forming organs |
|
D80–D89 |
Certain disorders involving the immune mechanism |
|
D50–D53 |
Nutritional anemias |
|
D55–D59 |
Haemolytic anaemias |
|
D60–D64 |
Aplastic and other anaemias |
|
D65–D69 |
Coagulation defects, purpura and other haemorrhagic conditions |
|
D70–D77 |
Other diseases of blood and blood-forming organs |
|
D50–D53 |
Nutritional anemias[edit] |
|
D50 |
Iron deficiency anaemia |
|
D50.0 |
Iron deficiency anaemia secondary to blood loss (chronic) |
|
D50.1 |
Sideropenic dysphagia Kelly-Paterson syndrome Plummer-Vinson syndrome |
|
D50.8 |
Other iron deficiency anaemias |
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D50.9 |
Iron deficiency anaemia, unspecified |
|
D51 |
Vitamin B12 deficiency anaemia |
|
D51.0 |
Vitamin B12 deficiency anaemia due to intrinsic factor deficiency Pernicious anemia |
|
D51.1 |
Vitamin B 12 deficiency anaemia due to selective vitamin B 12 malabsorption with proteinuria |
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|
Megaloblastic hereditary anaemia |
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D51.2 |
Transcobalamin II deficiency |
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D51.3 |
Other dietary vitamin B 12 deficiency anaemia |
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D51.8 |
Other vitamin B 12 deficiency anaemias |
|
D51.9 |
Vitamin B 12 deficiency anaemia, unspecified |
|
D52 |
Folate deficiency anaemia |
|
D52.0 |
Dietary folate deficiency anaemia Nutritional megaloblastic anaemia |
|
D52.1 |
Drug-induced folate deficiency anaemia |
|
D52.8 |
Other folate deficiency anaemias |
|
D52.9 |
Folate deficiency anaemia, unspecified |
|
D53 |
Other nutritional anaemias |
|
D53.0 |
Protein deficiency anaemia |
|
D53.1 |
Other megaloblastic anaemias, not elsewhere classified |
|
D53.2 |
Scorbutic anaemia |
|
D53.8 |
Other specified nutritional anaemias |
|
D53.9 |
Nutritional anaemia, unspecified |
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(D55–D59) Haemolytic anaemias |
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|
D55 |
Anaemia due to enzyme disorders |
|
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 |
|
D55.2 |
Anaemia due to disorders of glycolytic enzymes hexokinase deficiency pyruvate kinase 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 |
|
D56.0 |
Alpha thalassaemia |
|
D56.1 |
Beta thalassaemia |
|
D56.2 |
Delta-beta thalassaemia |
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D56.3 |
Thalassaemia trait |
|
D56.4 |
Hereditary persistence of fetal haemoglobin (HPFH) |
|
D56.8 |
Other thalassaemias |
|
D56.9 |
Thalassaemia, unspecified |
|
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 |
|
D58.0 |
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 Haemoglobinopathy NOS Unstable haemoglobin haemolytic disease |
|
D58.8 |
Other specified hereditary haemolytic anaemias Stomatocytosis |
|
D59 |
Acquired haemolytic anaemia |
|
D59.0 |
Drug-induced autoimmune haemolytic anaemia |
|
D59.1 |
Other autoimmune haemolytic anaemias Warm autoimmune hemolytic anemia |
|
D59.2 |
Drug-induce nonautoimmune haemolytic anaemia |
|
D59.3 |
Haemolytic-uraemic syndrome |
|
D59.4 |
Other nonautoimmune haemolytic anaemias Microangiopathic hemolytic anemia |
|
D59.5 |
Paroxysmal nocturnal haemoglobinuria (Marchiafava-Micheli) |
|
D59.6 |
Haemoglobinuria due to haemolysis from other external causes paroxysmal cold haemoglobinuria |
|
D59.8 |
Other acquired haemolytic anaemias |
|
D59.9 |
Acquired haemolytic anaemia, unspecified |
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(D60–D64) Aplastic and other anaemias |
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|
D60 |
Acquired pure red cell aplasia (erythroblastopenia) |
|
D61 |
Other aplastic anaemias |
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D61.0 |
Constitutional aplastic anaemia Blackfan-Diamond syndrome Familial hypoplastic anaemia Fanconi's anaemia Pancytopenia with malformations |
|
D61.1 |
Drug-induced aplastic anaemia |
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D61.2 |
Aplastic anaemia due to other external agents |
|
D61.3 |
Idiopathic aplastic anaemia |
|
D61.8 |
Other specified aplastic anaemias |
|
D61.9 |
Aplastic anaemia, unspecified Hypoplastic anaemia NOS Medullary hypoplasia Panmyelophthisis |
|
D62 |
Acute posthaemorrhagic anaemia |
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D63 |
Anaemia in chronic diseases classified elsewhere |
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D64 |
Other anaemias |
|
D64.0 |
Hereditary sideroblastic anaemia |
|
D64.1 |
Secondary sideroblastic anaemia due to disease |
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D64.2 |
Secondary sideroblastic anaemia due to drugs and toxins |
|
D64.3 |
Other sideroblastic anaemias |
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D64.4 |
Congenital dyserythropoietic anaemia |
|
D64.8 |
Other specified anaemias |
|
D64.9 |
Anaemia, unspecified |
