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All Diseases of the Blood and Immune Mechanism

Conditions of the blood, the blood-forming organs, and the mechanisms of immunity, following ICD-10 Chapter III (Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism). Belongs here: an autoimmune disease in which the immune system attacks the body's own tissue, an allergic reaction, and a disorder of blood cells or clotting not caused by cancer. Does not belong here: an autoimmune disease whose primary clinical presentation is confined to one organ system with its own chapter, such as an autoimmune skin condition, grouped under diseases of the skin and subcutaneous tissue.

Facts

Comparison

ICD-10 Chapter Number

III 1

ICD-10 Code Range

D50-D89 1

All Diseases of the Blood and Immune Mechanism

93 entries

Causative Agent

Era (First Described)

Treated By

Body System

ICD-10 Chapter

Communicable or Non-communicable

Transmission Route

1. ICD-10 (Wikipedia)

ICD-10 chapter table, Chapter III, chapter number
III | D50-D89 | "Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism"
ICD-10 chapter table, Chapter III, code range
III | D50-D89 | "Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism"

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Acute Hemolytic Transfusion Reaction

Agranulocytosis

AL amyloidosis

Allergic response

Anaphylaxis

Anemia

Antiphospholipid Syndrome

Antithrombin III Deficiency

Aplastic Anemia

Atypical hemolytic uremic syndrome

Autoimmune hemolytic anemia

Banti's syndrome

Bare lymphocyte syndrome

Behcet's Disease

Benign lymphoepithelial lesion

Castleman disease

Catastrophic antiphospholipid syndrome

Celiac Disease

Chronic Granulomatous Disease

Common Variable Immunodeficiency

Complement Deficiency

Delayed hemolytic transfusion reaction

Diamond-Blackfan anemia

Diffuse Infiltrative Lymphocytosis Syndrome

DiGeorge Syndrome

Disseminated Intravascular Coagulation

Emberger syndrome

Eosinophilia

Eosinophilia-myalgia syndrome

Exercise-induced anaphylaxis

Factor V Leiden

Fanconi anemia

Febrile non-hemolytic transfusion reaction

Fibrinolysis syndrome

Food Allergy

Gleich's syndrome

Glucose-6-Phosphate Dehydrogenase Deficiency

Goodpasture syndrome

Graft-Versus-Host Disease

Granulomatosis with Polyangiitis

Griscelli syndrome type 2

Guillain-Barre Syndrome

Harris platelet syndrome

Hemoglobin Lepore Syndrome

Hemolytic Anemia

Hereditary Spherocytosis

Hh blood group

Hughes-Stovin Syndrome

Hyperviscosity Syndrome

IgA Vasculitis

Immune reconstitution inflammatory syndrome

Immune Thrombocytopenic Purpura

Iron Deficiency Anemia

Kawasaki Disease

Leukotriene receptor antagonist-associated Churg-Strauss syndrome

LPS-responsive beige-like anchor protein deficiency

Macrophage activation syndrome

Mast Cell Activation Syndrome

McLeod syndrome

MonoMAC

Multiple Sclerosis

Myelodysplastic Syndrome

Myocarditis-myositis-myasthenia gravis overlap syndrome

Neutropenia

Paroxysmal nocturnal hemoglobinuria

Pernicious Anemia

Polycythemia Vera

Primary immunodeficiency

Psoriatic Arthritis

Rheumatoid Arthritis

Scleroderma

Serum Sickness

Severe Combined Immunodeficiency

Sideroblastic anemia

Sjogren Syndrome

Systemic Lupus Erythematosus

Thrombocytopenia

Thrombotic thrombocytopenic purpura

TNF receptor associated periodic syndrome

Transfusion hemosiderosis