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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

148 entries

Body System

ICD-10 Chapter

Communicable or Non-communicable

Causative Agent

Transmission Route

Era (First Described)

Treated By

Discoverer

Prevalence Band

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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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 D

Hemoglobin Lepore Syndrome

Hemolytic Anemia

Hereditary elliptocytosis

Hereditary persistence of fetal hemoglobin

Hereditary pyropoikilocytosis

Hereditary Spherocytosis

Hereditary stomatocytosis

Hh blood group

Hoyeraal-Hreidarsson syndrome

Hughes-Stovin Syndrome

Hyper IgM syndrome

Hypereosinophilic syndrome

Hyperimmunoglobulin E syndrome

Hyperviscosity Syndrome

Hypogammaglobulinemia

Hypoprothrombinemia

Idiopathic CD4+ lymphocytopenia

Idiopathic multicentric Castleman disease

IgA Vasculitis

Immune dysregulation

Immune reconstitution inflammatory syndrome

Immune Thrombocytopenic Purpura

Immunodeficiency-centromeric instability-facial anomalies syndrome

Iron Deficiency Anemia

Isolated congenital asplenia

Janus kinase 3 deficiency

Kawasaki Disease

Leukotriene receptor antagonist-associated Churg-Strauss syndrome

LIG4 syndrome

LPS-responsive beige-like anchor protein deficiency

Macrophage activation syndrome

Mast Cell Activation Syndrome

May-Hegglin anomaly

McLeod syndrome

Megaloblastic anemia

Microcytic anemia

MonoMAC