Contents 1 4. Diseases of the blood and blood-forming organs (280-289) 1.1 diseases of the blood and blood-forming organs (280-289) 1.1.1 anemia 1.1.2 coagulation/hemorrhagic 1.1.3 other 2 See also

[edit] 4. Diseases of the blood and blood-forming organs (280-289)

[edit] diseases of the blood and blood-forming organs (280-289)

[edit] anemia

• (280) Iron deficiency anemias
  • (280.0) Iron deficiency anemia, chronic blood loss
  • (280.1) Iron deficiency anemia, decreased intake

• (281) Other deficiency anemias
  • (281.0) pernicious anemia
  • (281.2) Anemia, folate deficiency
  • (281.3) Other specified megaloblastic anemias, not elsewhere classified

• (282) Hereditary hemolytic anemias
  • (282.0) Hereditary spherocytosis
  • (282.2) G6PD
  • (282.5) Sickle-cell trait
  • (282.6) Sickle-cell anemia

• (283) Acquired hemolytic anemias
  • (283.0) Autoimmune hemolytic anemias
    • Warm autoimmune hemolytic anemia
  • (283.1) Non-autoimmune hemolytic anemias
  • (283.2) Hemoglobinuria due to hemolysis from external causes
    • Paroxysmal nocturnal hemoglobinuria

• (284) Aplastic anemia
  • Fanconi anemia

• (285) Other and unspecified anemias
  • (285.9) Anemia, other, unspec.

[edit] coagulation/hemorrhagic

• (286) Coagulation defects
  • (286.0) Haemophilia A
  • (286.1) Haemophilia B
  • (286.2) Haemophilia C
  • (286.3) Congenital deficiency of other clotting factors
    • Factor XIII deficiency
  • (286.4) Von Willebrand's disease
  • (286.5) Hemorrhagic disorder due to intrinsic anticoagulants
  • (286.6) Defibrination syndrome
  • (286.7) Acquired coagulation factor deficiency
  • (286.9) Coagulation defects, other

• (287) Purpura and other hemorrhagic conditions
  • (287.0) Allergic purpura
    • Henoch-Schönlein purpura
  • (287.3) Thrombocytopenia, primary
    • (287.31) Immune thrombocytopenic purpura
      • Idiopathic thrombocytopenic purpura
  • (287.4) Thrombocytopenia, secondary
  • (287.9) Hemorrhagic conditions, unspec.

[edit] other

• (288) Diseases of white blood cells
  • (288.0) Leukopenia
  • (288.1) Functional disorders of polymorphonuclear neutrophils
  • (288.2) Genetic anomalies of leukocytes
  • (288.3) Eosinophilia
  • (288.4) Hemophagocytic syndromes
  • (288.5) Decreased white blood cell count
    • (288.50) Leukocytopenia, unspecified
    • (288.51) Lymphocytopenia
  • (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
  • (288.8) Other specified disease of white blood cells
  • (288.9) Abnormal white blood cells, unspec.

• (289) Other diseases of blood and blood-forming organs
  • (289.1) Lymphadenitis, chronic
  • (289.7) Methemoglobinemia
  • (289.8) Other specified diseases of blood and blood-forming organs
    • (289.81) Primary hypercoagulable state
      • Protein C deficiency
      • Protein S deficiency
      • Antithrombin III deficiency
    • (289.89) Other specified disease of blood and blood-forming organs

[edit] See also

• List of ICD-9 codes

v • d • e Pathology: Medical conditions (Diseases/Disorders/Illness, Syndromes/Sequences, Symptoms/Signs, Injuries, etc.) and ICD codes (A/B, 001-139) Infectious disease/Infection: Bacterial disease (G+, G-) · Virus disease · Parasitic disease (Protozoan infection, Helminthiasis, Ectoparasitic infestation) · Mycosis · Zoonosis (C/D, 140-239 & 280-289) Cancer (C00-D48, 140-239) Tumor Myeloid hematologic (D50-D77, 280-289) Anemia · Coagulopathy Lymphoid immune (D80-D89, 279) Immunodeficiency · Immunoproliferative disorder · Hypersensitivity (E, 240-278) Endocrine disease · Nutrition disorder · Inborn error of metabolism (F, 290-319) Mental disorder (G, 320-359) Nervous system disease (CNS, PNS) · Neuromuscular disease (H, 360-389) Eye disease · Ear disease (I, 390-459) Cardiovascular disease (Heart disease, Vascular disease) (J, 460-519) Respiratory disease (Obstructive lung disease, Restrictive lung disease, Pneumonia) (K, 520-579) Stomatognathic disease (Tooth disease) · Digestive disease (Esophageal, Stomach, Enteropathy, Liver, Pancreatic) (L, 680-709) Skin disease · skin appendages (Nail disease, Hair disease, Sweat gland disease) (M, 710-739) Musculoskeletal disorders · Osteochondropathy (Osteopathy, Chondropathy) (N, 580-629) Urologic disease (Nephropathy, Urinary bladder disease) · Male genital disease · Breast disease · Female genital disease (O, 630-679) Complications of pregnancy · Obstetric labor complication · Puerperal disorder (P, 760-779) Fetal disease (Q, 740-759) Congenital disorder (R, 780-799) Syndromes · Medical signs (Eponymous) (S/T, 800-999) Bone fracture · Joint dislocation · Sprain · Strain · subluxation · Head injury · Chest trauma · Poisoning

v • d • e Pathology: hematology · hematologic diseases of RBCs and megakaryocytes / MEP (D50-69,74, 280-287) Red blood cells ↑ Polycythemia Polycythemia vera ↓ Anemia Nutritional Micro-: Iron deficiency anemia (Plummer-Vinson syndrome) Macro-: Megaloblastic anemia (Pernicious anemia) Hemolytic (mostly Normo-) Hereditary enzymopathy: G6PD · glycolysis (PK, TI, HK) hemoglobinopathy: Thalassemia (alpha, beta, delta)  · Sickle-cell disease/trait · HPFH membrane: Hereditary spherocytosis (Minkowski-Chauffard syndrome) · Hereditary elliptocytosis (Ovalocytosis) · Hereditary stomatocytosis Acquired Autoimmune (WAHA, CAD, PCH) membrane (PNH) MAHA · TM (HUS) Drug-induced autoimmune · Drug-induced nonautoimmune Hemolytic disease of the newborn Aplastic (mostly Normo-) Hereditary: Fanconi anemia · Diamond-Blackfan anemia Acquired: PRCA · Sideroblastic anemia · Myelophthisic Blood tests MCV (Normocytic, Microcytic, Macrocytic) · MCHC (Normochromic, Hypochromic) Other Methemoglobinemia · Sulfhemoglobinemia · Reticulocytopenia Coagulation/ coagulopathy/ bleeding diathesis ↑ Thrombocytosis Essential thrombocytosis Hypercoagulability primary: Antithrombin III deficiency · Protein C deficiency/Activated protein C resistance/Protein S deficiency/Factor V Leiden · Hyperprothrombinemia acquired: DIC (Congenital afibrinogenemia, Purpura fulminans) · autoimmune (Antiphospholipid) ↓ Thrombocytopenia and purpura Nonthrombocytopenic purpura: Henoch-Schönlein purpura Thrombocytopenic purpura: ITP (Evans syndrome) · TM (TTP) Heparin-induced thrombocytopenia · May-Hegglin anomaly Platelet function adhesion (Bernard-Soulier syndrome) · aggregation (Glanzmann's thrombasthenia) · platelet storage pool deficiency (Hermansky-Pudlak syndrome, Gray platelet syndrome) Clotting factor Hemophilia (A/VIII, B/IX, C/XI) • Von Willebrand disease • Hypoprothrombinemia/II · XIII myeloid navs: cells/physio, disease of RBCs+megakaryocytes/monocytes+granulocytes/neoplasia, symptoms+signs/eponymous ↑ means increased, ↓ means decreased

v • d • e Lymphatic disease: splenic disease (D73/Q89.0, 289.4-289.5/759.0) Acquired Acquired asplenia/hyposplenism · Wandering spleen · Splenomegaly (Banti's syndrome) Congenital Congenital asplenia/hyposplenism · Accessory spleen · Polysplenia lymphatic organ navs: anat, physio, lymphatic disease/splenic disease/thymus disorders/thymus neoplasia/vascular tumors, proc