| dbo:abstract
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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 (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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- 34604 (xsd:nonNegativeInteger)
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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
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| dbp:date
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| dbp:reason
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- no files for 2006 are listed at the cited source, but files for 2013 are there; NLM releases this information annually (en)
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| dbp:wikiPageUsesTemplate
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| dct:subject
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| gold:hypernym
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| rdfs:comment
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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 (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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| rdfs:label
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- List of MeSH codes (C15) (en)
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