Browse By

III: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism

This dimension groups medical conditions by their ICD-10 chapter. Wikipedia notes that "there are four main types of disease: infectious diseases, deficiency diseases, hereditary diseases, and physiological diseases," a grouping that standard classification systems such as ICD-10 organize into their own numbered chapters. Browsing this way collects every condition classified under the same chapter.

Facts

Comparison

ICD-10 Chapter Number

III 1

ICD-10 Code Range

D50-D89 1

III: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism

93 entries

Causative Agent

Era (First Described)

Treated By

Body System

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"

Comments (0)

No comments yet. Be the first to share a thought.

Reader Challenges (0)

No disputes yet. Spotted an error or a better source? Open the first one.

Acute Hemolytic Transfusion Reaction

Agranulocytosis

Allergic response

Alpha-thalassemia

Anaphylaxis

Anemia

Antiphospholipid Syndrome

Antithrombin III Deficiency

Aplastic Anemia

Atypical hemolytic uremic syndrome

Autoimmune hemolytic anemia

Bare lymphocyte syndrome

Behcet's Disease

Benign lymphoepithelial lesion

Catastrophic antiphospholipid syndrome

Celiac Disease

Chronic Granulomatous Disease

Common Variable Immunodeficiency

Complement 2 deficiency

Complement Deficiency

Delayed hemolytic transfusion reaction

Diamond-Blackfan anemia

Diffuse Infiltrative Lymphocytosis Syndrome

DiGeorge Syndrome

Disseminated Intravascular Coagulation

DOCK8 deficiency

Emberger syndrome

Eosinophilia

Eosinophilia-myalgia syndrome

Exercise-induced anaphylaxis

Factor V Leiden

Factor XIII deficiency

Fanconi anemia

Febrile non-hemolytic transfusion reaction

Fibrinolysis syndrome

Food Allergy

Gleich's syndrome

Glucose-6-Phosphate Dehydrogenase Deficiency

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 pyropoikilocytosis

Hereditary Spherocytosis

Hughes-Stovin Syndrome

Hypereosinophilic syndrome

Hyperviscosity Syndrome

Hypoprothrombinemia

Idiopathic CD4+ lymphocytopenia

IgA Vasculitis

Immune reconstitution inflammatory syndrome

Immune Thrombocytopenic Purpura

Iron Deficiency Anemia

Isolated congenital asplenia

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

Rh deficiency syndrome

Rheumatoid Arthritis

Scleroderma

Serum Sickness

Severe Combined Immunodeficiency

Sideroblastic anemia