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) [edit]

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

Anemia (280–285) [edit]

(280) Iron deficiency anemias
- (280.0) Iron deficiency anemia secondary to blood loss (chronic)
- (280.1) Iron deficiency anemia secondary to inadequate dietary iron intake
- (280.8) Other specified iron deficiency anemias
- (280.9) Iron deficiency anemia, unspecified
(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) [edit]

(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) [edit]

(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 [edit]

List of ICD-9 codes

Pathology: Medical conditions and ICD code

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

(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 &
279–289)

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)

(S/T, 800–999)

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

↑

Poly- cythemia	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 Southeast Asian 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-)

MCV
MCHC
- Normochromic
- Hypochromic

Other

Coagulation/
coagulopathy

↑

Hyper- coagulability	primary: Antithrombin III deficiency Protein C deficiency/Activated protein C resistance/Protein S deficiency/Factor V Leiden Prothrombin G20210A acquired:Thrombocytosis essential DIC Congenital afibrinogenemia Purpura fulminans autoimmune Antiphospholipid

↓

Hypo-
coagulability

Thrombocytopenia	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 Dysfibrinogenemia

cell/phys (coag, heme, immu, gran), csfs

rbmg/mogr/tumr/hist, sysi/epon, btst

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

Lymphatic disease: Congenital lymphatic organ disorders (Q89.0/Q89.2, 759.0/759.2)

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

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