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D50 D50.0 D50.9 D51 D52 D53 D53.9 D64.9 D55.0 D56 D56.0 D56.1 D56.3 D56.8 D56.9 D57 D58 D59 D59.0 D59.1 Iron deficiency anaemia Incl.:anaemia:asiderotic, hypochromic Iron deficiency anaemia secondary to blood loss (chronic) Posthaemorrhagic anaemia (chronic) Iron deficiency anaemia, unspecified Vitamin B12 deficiency anaemia Folate deficiency anaemia Other nutritional anaemias Nutritional anaemia, unspecified Anaemia NOS Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency Thalassemia Alpha thalassaemia Beta thalassaemia Thalassaemia trait Other thalassaemias Thalassaemia, unspecified Sickle-cell disorders Other hereditary haemolytic anaemias Acquired haemolytic anaemia Drug-induced autoimmune haemolytic anaemia Other autoimmune haemolytic anaemias Autoimmune haemolytic disease (cold type)(warm type) Haemolytic anaemia: Evans syndrome Haemolytic-uraemic syndrome Constitutional aplastic anaemia, Aplasia, Blackfan-Diamond syndrome, Familial hypoplastic anaemia, Fanconi anaemia, Pancytopenia with malformations Drug-induced aplastic anaemia Disseminated intravascular coagulation (DIC) Hereditary factor VIII deficiency Hereditary factor IX deficiency Von Willebrand disease Idiopathic thrombocytopenic purpura (ITP) Agranulocytosis Incl.: Agranulocytic angina, Infantile genetic agranulocytosis, Kostmann disease, Neutropenia (NOS, congenital, cyclic, drug-induced, periodic, splenic [primary], toxic), Neutropenic splenomegaly,Werner-Schultz disease Use additional external cause code (Chapter XX), if desired, to identify drug, if drug-induced. Neutropenia, unspecified (febrile neutropenia) Hypersplenism Polycythaemia:benign, familial Secondary polycythemia Polycythaemia vera Polycythaemia neonatorum Langerhans-cell histiocytosis, multifocal Langerhans-cell histiocytosis, unifocal Malignant histiocytosis
Source: http://apps.who.int/classifications/icd10/browse/2010/en# Div. Hematologi Onkologi Ilmu kesehatan Anak FKUI/RSCM. Desember 2013
D69.3 D59.3 D61.0 D61.1 D65 D66 D67 D68.0 D69.3 D70