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List of MeSH codes (C20)

Summary

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 C20 – immune system diseases edit

MeSH C20.111 – autoimmune diseases edit

MeSH C20.111.163 – Addison disease edit

MeSH C20.111.175 – anemia, hemolytic, autoimmune edit

MeSH C20.111.190 – anti-glomerular basement membrane disease edit

MeSH C20.111.197 – antiphospholipid syndrome edit

MeSH C20.111.199 – arthritis, rheumatoid edit

MeSH C20.111.258 – autoimmune diseases of the nervous system edit

MeSH C20.111.318 – dermatitis herpetiformis edit

MeSH C20.111.327 – diabetes mellitus, type 1 edit

MeSH C20.111.375 – familial Mediterranean fever edit

MeSH C20.111.525 – glomerulonephritis, iga edit

MeSH C20.111.535 – glomerulonephritis, membranous edit

MeSH C20.111.550 – Goodpasture syndrome edit

MeSH C20.111.555 – Graves' disease edit

MeSH C20.111.567 – hepatitis, autoimmune edit

MeSH C20.111.580 – Lambert–Eaton myasthenic syndrome edit

MeSH C20.111.590 – lupus erythematosus, systemic edit

MeSH C20.111.709 – ophthalmia, sympathetic edit

MeSH C20.111.730 – pemphigoid, bullous edit

MeSH C20.111.736 – pemphigus edit

MeSH C20.111.750 – polyendocrinopathies, autoimmune edit

MeSH C20.111.759 – purpura, thrombocytopenic, idiopathic edit

MeSH C20.111.782 – Reiter disease edit

MeSH C20.111.809 – thyroiditis, autoimmune edit

MeSH C20.188 – blood group incompatibility edit

MeSH C20.188.413 – erythroblastosis, fetal edit

MeSH C20.188.780 – rh isoimmunization edit

MeSH C20.425 – glomerulonephritis, membranoproliferative edit

MeSH C20.452 – graft vs host disease edit

MeSH C20.543 – hypersensitivity edit

MeSH C20.543.206 – drug hypersensitivity edit

MeSH C20.543.312 – environmental illness edit

MeSH C20.543.418 – hypersensitivity, delayed edit

MeSH C20.543.480 – hypersensitivity, immediate edit

MeSH C20.543.520 – immune complex diseases edit

MeSH C20.543.600 – latex hypersensitivity edit

MeSH C20.543.928 – Wissler's syndrome edit

MeSH C20.673 – immunologic deficiency syndromes edit

MeSH C20.673.088 – agammaglobulinemia edit

MeSH C20.673.290 – ataxia–telangiectasia edit

MeSH C20.673.330 – common variable immunodeficiency edit

MeSH C20.673.340 – DiGeorge syndrome edit

MeSH C20.673.430 – dysgammaglobulinemia edit

MeSH C20.673.480 – hiv infections edit

MeSH C20.673.483 – deltaretrovirus infections edit

MeSH C20.673.600 – leukocyte-adhesion deficiency syndrome edit

MeSH C20.673.627 – lymphopenia edit

  • MeSH C20.673.627.800 – t-lymphocytopenia, idiopathic cd4-positive

MeSH C20.673.774 – phagocyte bactericidal dysfunction edit

MeSH C20.673.815 – severe combined immunodeficiency edit

MeSH C20.673.972 – Wiskott–Aldrich syndrome edit

MeSH C20.683 – immunoproliferative disorders edit

MeSH C20.683.460 – hypergammaglobulinemia edit

MeSH C20.683.515 – lymphoproliferative disorders edit

MeSH C20.683.780 – paraproteinemias edit

MeSH C20.841 – purpura, thrombocytopenic edit

MeSH C20.841.600 – purpura, thrombocytopenic, idiopathic edit

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

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