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).

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 C20immune system diseases[]

MeSH C20.111autoimmune diseases[]

MeSH C20.111.163Addison disease[]

MeSH C20.111.175anemia, hemolytic, autoimmune[]

MeSH C20.111.190anti-glomerular basement membrane disease[]

MeSH C20.111.197antiphospholipid syndrome[]

MeSH C20.111.199arthritis, rheumatoid[]

MeSH C20.111.258[]

MeSH C20.111.318dermatitis herpetiformis[]

MeSH C20.111.327diabetes mellitus, type 1[]

MeSH C20.111.375familial Mediterranean fever[]

MeSH C20.111.525glomerulonephritis, iga[]

MeSH C20.111.535glomerulonephritis, membranous[]

MeSH C20.111.550Goodpasture syndrome[]

MeSH C20.111.555Graves' disease[]

MeSH C20.111.567hepatitis, autoimmune[]

MeSH C20.111.580Lambert–Eaton myasthenic syndrome[]

MeSH C20.111.590lupus erythematosus, systemic[]

MeSH C20.111.709ophthalmia, sympathetic[]

MeSH C20.111.730pemphigoid, bullous[]

MeSH C20.111.736pemphigus[]

MeSH C20.111.750polyendocrinopathies, autoimmune[]

MeSH C20.111.759purpura, thrombocytopenic, idiopathic[]

MeSH C20.111.782Reiter disease[]

MeSH C20.111.809thyroiditis, autoimmune[]

MeSH C20.188[]

MeSH C20.188.413erythroblastosis, fetal[]

MeSH C20.188.780rh isoimmunization[]

MeSH C20.425glomerulonephritis, membranoproliferative[]

MeSH C20.452graft vs host disease[]

MeSH C20.543hypersensitivity[]

MeSH C20.543.206drug hypersensitivity[]

MeSH C20.543.312environmental illness[]

MeSH C20.543.418hypersensitivity, delayed[]

MeSH C20.543.480hypersensitivity, immediate[]

MeSH C20.543.520immune complex diseases[]

MeSH C20.543.600[]

MeSH C20.543.928Wissler's syndrome[]

MeSH C20.673immunologic deficiency syndromes[]

MeSH C20.673.088agammaglobulinemia[]

MeSH C20.673.290ataxia–telangiectasia[]

MeSH C20.673.330common variable immunodeficiency[]

MeSH C20.673.340DiGeorge syndrome[]

MeSH C20.673.430dysgammaglobulinemia[]

MeSH C20.673.480hiv infections[]

MeSH C20.673.483deltaretrovirus infections[]

MeSH C20.673.600leukocyte-adhesion deficiency syndrome[]

MeSH C20.673.627lymphopenia[]

MeSH C20.673.774phagocyte bactericidal dysfunction[]

MeSH C20.673.815severe combined immunodeficiency[]

MeSH C20.673.972Wiskott–Aldrich syndrome[]

MeSH C20.683immunoproliferative disorders[]

MeSH C20.683.460hypergammaglobulinemia[]

MeSH C20.683.515lymphoproliferative disorders[]

MeSH C20.683.780paraproteinemias[]

MeSH C20.841purpura, thrombocytopenic[]

MeSH C20.841.600purpura, thrombocytopenic, idiopathic[]


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

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