List of MeSH codes (C20)

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The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM).

Contents

This list continues the information at List of MeSH codes (C19). Codes following these are found at List of MeSH codes (C21). For other MeSH codes, see List of MeSH codes.

The source for this content is the set of 2006 MeSH Trees from the NLM.

MeSH   C20 – immune system diseases

MeSH   C20.111 – autoimmune diseases

MeSH   C20.111.163 – Addison disease

MeSH   C20.111.175 – anemia, hemolytic, autoimmune

MeSH   C20.111.190 – anti-glomerular basement membrane disease

MeSH   C20.111.197 – antiphospholipid syndrome

MeSH   C20.111.199 – arthritis, rheumatoid

MeSH   C20.111.258 – autoimmune diseases of the nervous system

MeSH   C20.111.318 – dermatitis herpetiformis

MeSH   C20.111.327 – diabetes mellitus, type 1

MeSH   C20.111.375 – familial Mediterranean fever

MeSH   C20.111.525 – glomerulonephritis, iga

MeSH   C20.111.535 – glomerulonephritis, membranous

MeSH   C20.111.550 – Goodpasture syndrome

MeSH   C20.111.555 – Graves' disease

MeSH   C20.111.567 – hepatitis, autoimmune

MeSH   C20.111.580 – Lambert–Eaton myasthenic syndrome

MeSH   C20.111.590 – lupus erythematosus, systemic

MeSH   C20.111.709 – ophthalmia, sympathetic

MeSH   C20.111.730 – pemphigoid, bullous

MeSH   C20.111.736 – pemphigus

MeSH   C20.111.750 – polyendocrinopathies, autoimmune

MeSH   C20.111.759 – purpura, thrombocytopenic, idiopathic

MeSH   C20.111.782 – Reiter disease

MeSH   C20.111.809 – thyroiditis, autoimmune

MeSH   C20.188 – blood group incompatibility

MeSH   C20.188.413 – erythroblastosis, fetal

MeSH   C20.188.780 – rh isoimmunization

MeSH   C20.425 – glomerulonephritis, membranoproliferative

MeSH   C20.452 – graft vs host disease

MeSH   C20.543 – hypersensitivity

MeSH   C20.543.206 – drug hypersensitivity

MeSH   C20.543.312 – environmental illness

MeSH   C20.543.418 – hypersensitivity, delayed

MeSH   C20.543.480 – hypersensitivity, immediate

MeSH   C20.543.520 – immune complex diseases

MeSH   C20.543.600 – latex hypersensitivity

MeSH   C20.543.928 – Wissler's syndrome

MeSH   C20.673 – immunologic deficiency syndromes

MeSH   C20.673.088 – agammaglobulinemia

MeSH   C20.673.290 – ataxia–telangiectasia

MeSH   C20.673.330 – common variable immunodeficiency

MeSH   C20.673.340 – DiGeorge syndrome

MeSH   C20.673.430 – dysgammaglobulinemia

MeSH   C20.673.480 – hiv infections

MeSH   C20.673.483 – deltaretrovirus infections

MeSH   C20.673.600 – leukocyte-adhesion deficiency syndrome

MeSH   C20.673.627 – lymphopenia

MeSH   C20.673.774 – phagocyte bactericidal dysfunction

MeSH   C20.673.815 – severe combined immunodeficiency

MeSH   C20.673.972 – Wiskott–Aldrich syndrome

MeSH   C20.683 – immunoproliferative disorders

MeSH   C20.683.460 – hypergammaglobulinemia

MeSH   C20.683.515 – lymphoproliferative disorders

MeSH   C20.683.780 – paraproteinemias

MeSH   C20.841 – purpura, thrombocytopenic

MeSH   C20.841.600 – purpura, thrombocytopenic, idiopathic

The list continues at List of MeSH codes (C21).

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