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ICD Codes And Descriptions for Blood and Blood-Forming Organs

280. Iron deficiency anemias
280.0 Iron deficiency anemia secondary to blood loss (chronic)
280.1 Iron Def Anemia Dietary
280.8 Iron Defic Anemia Nec
280.9 Iron deficiency anemia, unspecified
281. Other deficiency anemias
281.0 Pernicious anemia
281.1 Other vitamin B12 deficiency anemia
281.2 Folate-deficiency anemia
281.3 Megaloblastic Anemia Nec
281.4 Protein Defic Anemia
281.8 Nutritional Anemia Nec
281.9 Unspecified deficiency anemia (nutritional anemia)
282. Hereditary hemolytic anemias
282.0 Hereditary Spherocytosis
282.1 Heredit Elliptocytosis
282.2Glucose-6-phosphate dehydrogenase deficiency; anemias due to disorders of glutathione metabolism
282.3 Other hemolytic anemias due to enzyme deficiency
282.4 Thalassemia
282.41 Sickle-cell thalassemia without crisis
282.42 Sickle-cell thalassemia with crisis; vaso-occlusive crisis; vaso-occlusive pain
282.44 Beta-Thalassemia
282.49 Other thalassemia
282.5 Sickle cell trait
282.6 Sickle cell disease; sickle cell anemia
282.60 Sickle-cell anemia not otherwise stated
282.61 Hb-s Disease Without Crisis
282.62 Hb-S disease with mention of crisis
282.63 Sickle-cell/hb-c Disease
282.64 Sickle-cell/HB-C disease with crisis
282.68 Other sickle-cell disease without crisis
282.69 Sickle-cell Anemia Nec
282.7 Other hemoglobinopathies; persistent fetal hemoglobin
282.8 Hered Hemolytic Anem Nec
282.9 Hereditary hemolytic anemia, unspecified
283. Acquired hemolytic anemias
283.0 Autoimmune hemolytic anemias
283.1 Non-autoimmune hemolytic anemias
283.10 Nonauto Hem Anemia Nos
283.11 Hemolytic Uremic Syndrome
283.19 Other non-autoimmune hemolytic anemias; acquired thrombotic thrombocytopenic purpura
283.2 Hemoglobinuria due to hemolysis from external causes
283.9 Acquired hemolytic anemia, unspecified
284. Aplastic anemia
284.0 Constitutional aplastic anemia
284.01 Constitutional red blood cell aplasia; pure red-cell aplasia
284.09 Other constitutional aplastic anemia; Fanconi's anemia
284.1 Pancytopenia
284.2 Myelophthisis
284.8 Other specified aplastic anemias
284.81 Red cell aplasia; pure red cell aplasia
284.89 Other specified aplastic anemias
284.9 Unspecified aplastic anemia
285. Other and unspecified anemias
285.0 Sideroblastic anemia
285.1 Acute posthemorrhagic anemia (due to acute blood loss)
285.2 Anemia in chronic illness
285.21 Anemia In Esrd
285.22 Anemia In Neoplastic Dis
285.29 Anemia-oth Chronic Ill
285.3 Antineoplastic chemotherapy induced anemia
285.8 Other specified anemias
285.9 Unspecified anemia
286. Coagulation defects
286.0 Hemophilia; hemophilia A (factor VIII deficiency); hemophilia B (factor IX deficiency; Christmas disease)
286.1 Congenital factor IX disorder; hemophilia B; Christmas disease
286.2 Congenital factor XI deficiency
286.3 Factor deficiencies (factor I deficiency, factor II deficiency, factor V deficiency, factor V plus VIII deficiency, factor VII deficiency, factor X deficiency, factor XIII deficiency); congenital deficiency of other clotting factors
286.4 von Willebrand disease
286.5 Hemorrhagic disorder due to circulating anticoagulants (increase in anti-VIIIa, IXa, Xa)
286.6 Defibrination syndrome (disseminated intravascular coagulation, DIC)
286.7 Acquired coagulation factor deficiency; acquired hemophilia
286.9 Other and unspecified coagulation defects; thrombophilia
287. Purpura and other hemorrhagic conditions
287.0 Allergic purpura; Henoch-Schonlein purpura (IgA vasculitis)
287.1 Thrombocytopathy; Glanzmanns Thrombasthenia; Bernard Soulier Syndrome
287.2 Purpura Nos
287.3 Primary thrombocytopenia
287.30 Primary thrombocytopenia unspecified
287.31 Immune thrombocytopenic purpura; idiopathic thrombocytopenic purpura; tidal platelet dysgenesis
287.32 Evans' syndrome
287.33 Congenital and hereditary thrombocytopenic purpura
287.39 Congenital and hereditary thrombocytopenic purpura; Congenital and hereditary thrombocytopenia; Thrombocytopenia with absent radii (TAR) syndrome
287.4 Secondary thrombocytopenia; thrombocytopenia (platelet deficiency); drug-induced thrombocytopenia
287.5 Thrombocytopenia, unspecified
287.8 Hemorrhagic Cond Nec
287.9 Hemorrhagic Cond Nos
288. Diseases of white blood cells (WBC)
288.0 Agranulocytosis (neutropenia)
288.00 Neutropenia, unspecified
288.01 Congenital neutropenia
288.02 Cyclic neutropenia
288.03 Drug induced neutropenia
288.04 Neutropenia due to infection
288.09 Other neutropenia
288.1 Functional disorders of polymorphonuclear neutrophils
288.2 Genetic Anomaly Leukocyt
288.3 Eosinophilia; hypereosinophilic syndrome
288.4 Hemophagocytic syndromes
288.5 Decreased white blood cell count
288.50 Leukocytopenia, unspecified
288.51 Lymphocytopenia
288.59 Other decreased white blood cell count
288.6 Elevated white blood cell count
288.60 Leukocytosis, unspecified
288.61 Lymphocytosis (symptomatic)
288.62 Leukemoid reaction
288.63 Monocytosis (symptomatic)
288.64 Plasmacytosis
288.65 Basophilia
288.66 Bandemia
288.69 Other elevated white blood cell count
288.8 Other specified disease of white blood cells (WBC)
288.9 Wbc Disease Nos
289. Other diseases of blood and blood-forming organs
289.0 Secondary polycythemia
289.1 Chronic lymphadenitis
289.2 Nonspecific mesenteric lymphadenitis
289.3 Lymphadenitis unspecified
289.4 Hypersplenism
289.5 Other diseases of spleen
289.50 Spleen Disease Nos
289.51 Chr Congest Splenomegaly
289.52 Splenic sequestration
289.53 Neutropenic splenomegaly
289.59 Other diseases of spleen
289.6 Familial Polycythemia
289.7 Methemoglobinemia
289.8 Other specified diseases of blood and blood-forming organs
289.81 Primary hypercoagulable state
289.82 Secondary hypercoagulable state
289.83 Myelofibrosis; Primary Myelofibrosis
289.84 Heparin-induced thrombocytopenia (HIT); heparin-induced thrombocytopenia and thrombosis (HITT)
289.89 Other specified diseases of blood and blood-forming organs
289.9 Unspecified diseases of blood and blood-forming organs