List of ICD-9 codes 280-289: diseases of the blood and blood-forming organs

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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)
2 See also

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

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

anemia (280-285)

(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

(285) Other and unspecified anemias
- (285.0) Sideroblastic anemia
- (285.1) Acute posthemorrhagic anemia
- (285.2) Anemia in chronic illness
- (285.3) Antineoplastic chemotherapy induced anemia
- (285.8) Other specified anemias
- (285.9) Anemia unspecified

coagulation/hemorrhagic (286-287)

(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.

other (288-289)

(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

See also

List of ICD-9 codes

Pathology: Medical conditions and ICD code

(Disease / Disorder / Illness, Syndrome / Sequence, Symptom / Sign, Injury, etc.)

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

Endocrine disease · Nutrition disorder · Inborn error of metabolism

Mental disorder

Nervous system disease (CNS, PNS) · Neuromuscular disease

Eye disease · Ear disease

Cardiovascular disease (Heart disease, Vascular disease)

Respiratory disease (Obstructive lung disease, Restrictive lung disease, Pneumonia)

Stomatognathic disease (Tooth disease) · Digestive disease (Esophageal, Stomach, Enteropathy, Liver, Pancreatic)

Skin disease · skin appendages (Nail disease, Hair disease, Sweat gland disease)

Musculoskeletal disorders: Myopathy · Arthropathy · Osteochondropathy (Osteopathy, Chondropathy)

Urologic disease (Nephropathy, Urinary bladder disease) · Male genital disease · Breast disease · Female genital disease

Complications of pregnancy · Obstetric labor complication · Puerperal disorder

Congenital disorder (Congenital abnormality)

Syndromes · Medical signs (Eponymous)

Bone fracture · Joint dislocation · Sprain · Strain · Subluxation · Head injury · Chest trauma · Poisoning

Pathology: hematology · hematologic diseases of RBCs and megakaryocytes / MEP (D50-69,74, 280-287)

Red
blood cells

↑

Polycythemia	Polycythemia vera

↓

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

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

cell/phys (coag, heme, gran)

rbmg/mogr/tumr, sysi/epon, btst

drug (B1/2/3+5+6), btst

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

anat(h, u, t, a, l)/phys

lydi/spdi/thdi/thtu/vatu

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