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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

Uses International Classification

WHO ICD-10 1

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

109 entries

Causative Agent

Era (First Described)

Treated By

Body System

Communicable or Non-communicable

Transmission Route

Showing the first 400 of 2,363 connections.

Sources

1. ICD-10 (Wikipedia)

lead paragraph

Quote, lead paragraph

ICD-10 is the 10th revision of the International Classification of Diseases (ICD), a medical classification list by the World Health Organization (WHO).

The Greatest Benefit to Mankind: A Medical History of Humanity

Roy Porter, W. W. Norton and Company, 1997Contains: HIV/AIDS

A History of Medicine

Lois N. Magner, CRC PressContains: Chronic Kidney Disease

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Acute Hemolytic Transfusion Reaction

Adenosine deaminase 2 deficiency

Adenosine deaminase deficiency

Agranulocytosis

Allergic response

Alpha-thalassemia

Anaphylaxis

Anemia

Antiphospholipid Syndrome

Antithrombin III Deficiency

Aplastic Anemia

ATR-X syndrome

Atypical hemolytic uremic syndrome

Autoimmune hemolytic anemia

Bare lymphocyte syndrome

Bare lymphocyte syndrome type II

Behcet's Disease

Benign lymphoepithelial lesion

Beta thalassemia

Catastrophic antiphospholipid syndrome

CD25 deficiency

Celiac Disease

Chronic Granulomatous Disease

Combined immunodeficiencies

Common Variable Immunodeficiency

Complement 2 deficiency

Complement Deficiency

Cyclic neutropenia

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

Hyperimmunoglobulin E syndrome

Hyperviscosity Syndrome

Hypogammaglobulinemia

Hypoprothrombinemia

Idiopathic CD4+ lymphocytopenia

IgA Vasculitis

Immune reconstitution inflammatory syndrome

Immune Thrombocytopenic Purpura

Immunodeficiency-centromeric instability-facial anomalies syndrome

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

Megaloblastic anemia

MonoMAC

Multiple Sclerosis

Myelodysplastic Syndrome

Myocarditis-myositis-myasthenia gravis overlap syndrome