| dbo:abstract |
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 (C14). Codes following these are found at List of MeSH codes (C16). For other MeSH codes, see List of MeSH codes. The source for this content is the set of 2006 MeSH Trees from the NLM. (en) |
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https://www.nlm.nih.gov/mesh/filelist.html |
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dbr:Pseudolymphoma dbr:Pseudoxanthoma_elasticum dbr:Sarcoidosis dbr:Eosinophilia dbr:Eosinophilic_granuloma dbr:Factor_xiii_deficiency dbr:Anemia,_aplastic dbr:Anemia,_diamond-blackfan dbr:Anemia,_hemolytic dbr:Anemia,_hemolytic,_autoimmune dbr:Anemia,_hypochromic dbr:Anemia,_hypoplastic,_congenital dbr:Anemia,_iron-deficiency dbr:Anemia,_macrocytic dbr:Anemia,_megaloblastic dbr:Anemia,_myelophthisic dbr:Anemia,_pernicious dbr:Anemia,_refractory dbr:Anemia,_refractory,_with_excess_of_blasts dbr:Anemia,_sickle_cell dbr:Anemia,_sideroblastic dbr:Hypereosinophilic_syndrome dbr:United_States_National_Library_of_Medicine dbr:Dysgammaglobulinemia dbr:Leukocytosis dbr:Leukopenia dbr:Leukostasis dbr:Thymus_hyperplasia dbr:Pelger-huet_anomaly dbr:Platelet_storage_pool_deficiency dbr:Thrombocytosis dbr:Multiple_myeloma dbr:Mycosis_fungoides dbr:Myelofibrosis dbr:Cryoglobulinemia dbc:Medical_Subject_Headings dbr:Protein_c_deficiency dbr:Protein_s_deficiency dbr:Anemia dbr:Leukemoid_reaction dbr:Lymphangioleiomyomatosis dbr:Lymphoma dbr:Lymphopenia dbr:Hemoglobinuria dbr:Kernicterus dbr:Tumor_lysis_syndrome dbr:Medical_Subject_Headings dbr:Pancytopenia dbr:Burkitt_lymphoma dbr:Agranulocytosis dbr:Alpha-thalassemia dbr:Fanconi_anemia dbr:Favism dbr:Angiolymphoid_hyperplasia_with_eosinophilia dbr:Bernard-soulier_syndrome dbr:Beta-thalassemia dbr:Granuloma dbr:Histiocytic_necrotizing_lymphadenitis dbr:Histiocytosis dbr:Eosinophilia-myalgia_syndrome dbr:Erdheim-chester_disease dbr:List_of_MeSH_codes dbr:List_of_MeSH_codes_(C14) dbr:List_of_MeSH_codes_(C16) dbr:King's_evil dbr:Purpura dbr:Heavy_chain_disease dbr:Hemolytic-uremic_syndrome dbr:Activated_protein_c_resistance dbr:Thalassemia dbr:Hydrops_fetalis dbr:Hypergammaglobulinemia dbr:Hypoalbuminemia dbr:Hypoproteinemia dbr:Shwartzman_phenomenon dbr:Abetalipoproteinemia dbr:Ehlers-danlos_syndrome dbr:Hemoglobinopathies dbr:Igg_deficiency dbr:Disseminated_intravascular_coagulation dbr:Polycythemia_vera dbr:Factor_v_deficiency dbr:Factor_vii_deficiency dbr:Factor_x_deficiency dbr:Factor_xi_deficiency dbr:Factor_xii_deficiency dbr:Granulomatous_disease,_chronic dbr:Mesenteric_lymphadenitis dbr:Telangiectasia,_hereditary_hemorrhagic dbr:Infectious_mononucleosis dbr:Antithrombin_iii_deficiency dbr:Methemoglobinemia dbr:Cat-scratch_disease dbr:Scurvy dbr:Churg–Strauss_syndrome dbr:Neutropenia dbr:Chediak-higashi_syndrome dbr:Lymphatic_filariasis dbr:Lymphangitis dbr:Lymphedema dbr:Lymphocele dbr:Lymphocytosis dbr:Lymphomatoid_granulomatosis dbr:Lymphoproliferative_disorders dbr:Sickle_cell_trait dbr:Mucocutaneous_lymph_node_syndrome dbr:Thrombophilia dbr:Polycythemia dbr:Lymphoma,_high-grade dbr:Lymphoma,_intermediate-grade dbr:Lymphoma,_low-grade dbr:Paroxysmal_hemoglobinuria_(disambiguation) dbr:Phagocyte_bactericidal_dysfunction dbr:Reticuloendotheliosis dbr:Wandering_spleen dbr:Sulfhemoglobinemia dbr:Thrombocytopenia dbr:Poems_syndrome dbr:Vitamin_k_deficiency dbr:Von_willebrand_disease dbr:Wiskott-aldrich_syndrome dbr:Afibrinogenemia dbr:Agammaglobulinemia dbr:Hodgkin_disease dbr:Job's_syndrome dbr:Splenic_infarction dbr:Splenosis dbr:Bone_marrow_diseases dbr:Bone_marrow_neoplasms dbr:Sarcoidosis,_pulmonary dbr:Vascular_hemostatic_disorders dbr:Waterhouse-friderichsen_syndrome dbr:Hypersplenism dbr:Hypoprothrombinemias dbr:Sezary_syndrome dbr:Leukemia,_erythroblastic,_acute dbr:Leukemia,_hairy_cell dbr:Leukemia,_lymphocytic dbr:Leukemia,_monocytic,_acute dbr:Leukemia,_myelocytic,_acute dbr:Leukemia,_myeloid dbr:Leukocyte_disorders dbr:Paraproteinemias dbr:Elliptocytosis,_hereditary dbr:Fetofetal_transfusion dbr:Hemangioma,_cavernous dbr:Hemangioma,_cavernous,_central_nervous_system dbr:Niemann-pick_diseases dbr:Gaucher_disease dbr:Blood_coagulation_disorders dbr:Blood_platelet_disorders dbr:Blood_protein_disorders dbr:Mast-cell_sarcoma dbr:Rh_isoimmunization dbr:Hermanski-pudlak_syndrome dbr:Glucosephosphate_dehydrogenase_deficiency dbr:Iga_deficiency dbr:Immunoblastic_lymphadenopathy dbr:Immunoproliferative_small_intestinal_disease dbr:Myelodysplastic_syndromes dbr:Myeloid_metaplasia dbr:Myeloproliferative_disorders dbr:Pulmonary_eosinophilia dbr:Purpura,_hyperglobulinemic dbr:Purpura,_schoenlein-henoch dbr:Purpura,_thrombocytopenic dbr:Purpura,_thrombocytopenic,_idiopathic dbr:Purpura,_thrombotic_thrombocytopenic dbr:Red-cell_aplasia,_pure dbr:Thrombasthenia dbr:Thymus_neoplasms dbr:Uveoparotid_fever dbr:Erythroblastosis,_fetal dbr:Waldenstrom_macroglobulinemia dbr:Coagulation_protein_disorders dbr:Lymphadenitis dbr:Lymphangiectasis dbr:Lymphatic_diseases dbr:Lymphohistiocytosis,_hemophagocytic dbr:Lymphoma,_aids-related dbr:Lymphoma,_b-cell dbr:Lymphoma,_diffuse dbr:Lymphoma,_follicular dbr:Lymphoma,_large-cell dbr:Lymphoma,_large-cell,_diffuse dbr:Lymphoma,_large-cell,_follicular dbr:Lymphoma,_large-cell,_immunoblastic dbr:Lymphoma,_large-cell,_ki-1 dbr:Lymphoma,_lymphoblastic dbr:Lymphoma,_mantle-cell dbr:Lymphoma,_mucosa-associated_lymphoid_tissue dbr:Lymphoma,_non-hodgkin dbr:Lymphoma,_small-cell dbr:Lymphoma,_small_cleaved-cell,_diffuse dbr:Lymphoma,_small_cleaved-cell,_follicular dbr:Lymphoma,_t-cell dbr:Lymphoma,_t-cell,_cutaneous dbr:Lymphoma,_t-cell,_peripheral dbr:Sea-blue_histiocyte_syndrome dbr:Hematologic_diseases dbr:Hematologic_neoplasms dbr:Hemoglobin_c_disease dbr:Hemophilia_a dbr:Hemophilia_b dbr:Hemorrhagic_disease_of_newborn dbr:Hemorrhagic_disorders dbr:Histiocytosis,_langerhans-cell dbr:Histiocytosis,_malignant dbr:Histiocytosis,_non-langerhans-cell dbr:Marek_disease dbr:Monoclonal_gammopathies,_benign dbr:Pregnancy_complications,_hematologic dbr:Preleukemia dbr:Spherocytosis,_hereditary dbr:Splenic_diseases dbr:Splenic_rupture dbr:Xanthogranuloma,_juvenile dbr:Anemia,_dyserythropoietic,_congenital dbr:Anemia,_hemolytic,_congenital dbr:Anemia,_hemolytic,_congenital_nonspherocytic dbr:Anemia,_neonatal dbr:Blood_coagulation_disorders,_inherited dbr:Blood_group_incompatibility dbr:Fetomaternal_transfusion dbr:Giant_lymph_node_hyperplasia dbr:Hemic_and_lymphatic_diseases dbr:Hemoglobin_sc_disease dbr:Histiocytic_disorders,_malignant dbr:Histiocytosis,_sinus dbr:Leukemia,_nonlymphocytic,_acute dbr:Lymphangiectasis,_intestinal dbr:Lymphatic_abnormalities dbr:Lymphoma,_mixed-cell dbr:Lymphoma,_mixed-cell,_diffuse dbr:Lymphoma,_mixed-cell,_follicular dbr:Lymphoma,_small_lymphocytic dbr:Lymphoma,_small_noncleaved-cell dbr:Lymphoma,_undifferentiated dbr:Splenic_neoplasms dbr:T-lymphocytopenia,_idiopathic_cd4-positive dbr:Thrombocythemia,_hemorrhagic dbr:Tuberculosis,_lymph_node dbr:Tuberculosis,_splenic dbr:Lymphangiomyoma |
| dbp:date |
February 2020 (en) |
| dbp:reason |
no files for 2006 are listed at the cited source, but files for 2013 are there; NLM releases this information annually (en) |
| dbp:wikiPageUsesTemplate |
dbt:Update dbt:MeSH_codes dbt:MeSH_number |
| dcterms:subject |
dbc:Medical_Subject_Headings |
| gold:hypernym |
dbr:List |
| rdfs:comment |
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 (C14). Codes following these are found at List of MeSH codes (C16). For other MeSH codes, see List of MeSH codes. The source for this content is the set of 2006 MeSH Trees from the NLM. (en) |
| rdfs:label |
List of MeSH codes (C15) (en) |
| owl:sameAs |
wikidata:List of MeSH codes (C15) https://global.dbpedia.org/id/4qSYZ |
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wikipedia-en:List_of_MeSH_codes_(C15)?oldid=1071994810&ns=0 |
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wikipedia-en:List_of_MeSH_codes_(C15) |
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dbr:List_of_MeSH_codes dbr:List_of_MeSH_codes_(C14) dbr:List_of_MeSH_codes_(C16) |
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wikipedia-en:List_of_MeSH_codes_(C15) |
