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List of MeSH codes (C15)

This article needs to be updated. The reason given is: no files for 2006 are listed at the cited source, but files for 2013 are there; NLM releases this information annually. Please help update this article to reflect recent events or newly available information. (February 2020)

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.

MeSH C15 – hemic and lymphatic diseases

MeSH C15.378 – hematologic diseases

MeSH C15.378.071 – anemia

MeSH C15.378.071.085 – anemia, aplastic
MeSH C15.378.071.085.080 – anemia, hypoplastic, congenital
MeSH C15.378.071.085.080.090 – anemia, diamond-blackfan
MeSH C15.378.071.085.080.280 – fanconi anemia
MeSH C15.378.071.141 – anemia, hemolytic
MeSH C15.378.071.141.125 – anemia, hemolytic, autoimmune
MeSH C15.378.071.141.150 – anemia, hemolytic, congenital
MeSH C15.378.071.141.150.095 – anemia, dyserythropoietic, congenital
MeSH C15.378.071.141.150.100 – anemia, hemolytic, congenital nonspherocytic
MeSH C15.378.071.141.150.150 – anemia, sickle cell
MeSH C15.378.071.141.150.150.440 – hemoglobin sc disease
MeSH C15.378.071.141.150.150.670 – sickle cell trait
MeSH C15.378.071.141.150.365 – elliptocytosis, hereditary
MeSH C15.378.071.141.150.480 – glucosephosphate dehydrogenase deficiency
MeSH C15.378.071.141.150.480.370 – favism
MeSH C15.378.071.141.150.490 – hemoglobin c disease
MeSH C15.378.071.141.150.785 – spherocytosis, hereditary
MeSH C15.378.071.141.150.875 – thalassemia
MeSH C15.378.071.141.150.875.100 – alpha-thalassemia
MeSH C15.378.071.141.150.875.150 – beta-thalassemia
MeSH C15.378.071.141.370 – favism
MeSH C15.378.071.141.510 – hemoglobinuria
MeSH C15.378.071.141.510.460 – hemoglobinuria, paroxysmal
MeSH C15.378.071.141.610 – hemolytic-uremic syndrome
MeSH C15.378.071.196 – anemia, hypochromic
MeSH C15.378.071.196.300 – anemia, iron-deficiency
MeSH C15.378.071.252 – anemia, macrocytic
MeSH C15.378.071.252.196 – anemia, megaloblastic
MeSH C15.378.071.252.196.500 – anemia, pernicious
MeSH C15.378.071.307 – anemia, myelophthisic
MeSH C15.378.071.363 – anemia, neonatal
MeSH C15.378.071.363.344 – fetofetal transfusion
MeSH C15.378.071.363.511 – fetomaternal transfusion
MeSH C15.378.071.400 – anemia, refractory
MeSH C15.378.071.400.080 – anemia, refractory, with excess of blasts
MeSH C15.378.071.419 – anemia, sideroblastic
MeSH C15.378.071.750 – red-cell aplasia, pure
MeSH C15.378.071.750.500 – anemia, diamond-blackfan

MeSH C15.378.100 – blood coagulation disorders

MeSH C15.378.100.141 – coagulation protein disorders
MeSH C15.378.100.141.036 – activated protein c resistance
MeSH C15.378.100.141.072 – afibrinogenemia
MeSH C15.378.100.141.300 – factor v deficiency
MeSH C15.378.100.141.310 – factor vii deficiency
MeSH C15.378.100.141.320 – factor x deficiency
MeSH C15.378.100.141.325 – factor xi deficiency
MeSH C15.378.100.141.330 – factor xii deficiency
MeSH C15.378.100.141.335 – factor xiii deficiency
MeSH C15.378.100.141.500 – hemophilia a
MeSH C15.378.100.141.510 – hemophilia b
MeSH C15.378.100.141.550 – hypoprothrombinemias
MeSH C15.378.100.141.900 – von willebrand disease
MeSH C15.378.100.220 – disseminated intravascular coagulation
MeSH C15.378.100.425 – blood coagulation disorders, inherited
MeSH C15.378.100.425.037 – activated protein c resistance
MeSH C15.378.100.425.056 – afibrinogenemia
MeSH C15.378.100.425.075 – antithrombin iii deficiency
MeSH C15.378.100.425.080 – bernard-soulier syndrome
MeSH C15.378.100.425.300 – factor v deficiency
MeSH C15.378.100.425.310 – factor vii deficiency
MeSH C15.378.100.425.320 – factor x deficiency
MeSH C15.378.100.425.325 – factor xi deficiency
MeSH C15.378.100.425.330 – factor xii deficiency
MeSH C15.378.100.425.335 – factor xiii deficiency
MeSH C15.378.100.425.500 – hemophilia a
MeSH C15.378.100.425.510 – hemophilia b
MeSH C15.378.100.425.515 – hermanski-pudlak syndrome
MeSH C15.378.100.425.550 – hypoprothrombinemias
MeSH C15.378.100.425.690 – protein c deficiency
MeSH C15.378.100.425.820 – thrombasthenia
MeSH C15.378.100.425.900 – von willebrand disease
MeSH C15.378.100.425.970 – wiskott-aldrich syndrome
MeSH C15.378.100.685 – platelet storage pool deficiency
MeSH C15.378.100.685.400 – hermanski-pudlak syndrome
MeSH C15.378.100.800 – protein s deficiency
MeSH C15.378.100.802 – purpura
MeSH C15.378.100.802.250 – purpura, hyperglobulinemic
MeSH C15.378.100.802.375 – purpura, schoenlein-henoch
MeSH C15.378.100.802.500 – purpura, thrombocytopenic
MeSH C15.378.100.805 – purpura, thrombocytopenic
MeSH C15.378.100.805.600 – purpura, thrombocytopenic, idiopathic
MeSH C15.378.100.805.680 – purpura, thrombotic thrombocytopenic
MeSH C15.378.100.805.972 – wiskott-aldrich syndrome
MeSH C15.378.100.832 – thrombocythemia, hemorrhagic
MeSH C15.378.100.920 – vitamin k deficiency
MeSH C15.378.100.920.360 – hemorrhagic disease of newborn

MeSH C15.378.120 – blood group incompatibility

MeSH C15.378.120.413 – erythroblastosis, fetal
MeSH C15.378.120.413.480 – hydrops fetalis
MeSH C15.378.120.413.502 – kernicterus
MeSH C15.378.120.780 – rh isoimmunization

MeSH C15.378.140 – blood platelet disorders

MeSH C15.378.140.120 – bernard-soulier syndrome
MeSH C15.378.140.735 – platelet storage pool deficiency
MeSH C15.378.140.735.400 – hermanski-pudlak syndrome
MeSH C15.378.140.810 – thrombasthenia
MeSH C15.378.140.855 – thrombocytopenia
MeSH C15.378.140.855.313 – hemolytic-uremic syndrome
MeSH C15.378.140.855.700 – purpura, thrombocytopenic
MeSH C15.378.140.855.700.600 – purpura, thrombocytopenic, idiopathic
MeSH C15.378.140.855.700.680 – purpura, thrombotic thrombocytopenic
MeSH C15.378.140.855.700.972 – wiskott-aldrich syndrome
MeSH C15.378.140.860 – thrombocytosis
MeSH C15.378.140.860.800 – thrombocythemia, hemorrhagic
MeSH C15.378.140.900 – von willebrand disease

MeSH C15.378.147 – blood protein disorders

MeSH C15.378.147.068 – abetalipoproteinemia
MeSH C15.378.147.142 – agammaglobulinemia
MeSH C15.378.147.150 – antithrombin iii deficiency
MeSH C15.378.147.333 – dysgammaglobulinemia
MeSH C15.378.147.333.500 – iga deficiency
MeSH C15.378.147.333.750 – igg deficiency
MeSH C15.378.147.542 – hypergammaglobulinemia
MeSH C15.378.147.542.640 – monoclonal gammopathies, benign
MeSH C15.378.147.607 – hypoproteinemia
MeSH C15.378.147.607.500 – hypoalbuminemia
MeSH C15.378.147.780 – paraproteinemias
MeSH C15.378.147.780.243 – cryoglobulinemia
MeSH C15.378.147.780.490 – heavy chain disease
MeSH C15.378.147.780.490.512 – immunoproliferative small intestinal disease
MeSH C15.378.147.780.650 – multiple myeloma
MeSH C15.378.147.780.750 – poems syndrome
MeSH C15.378.147.780.925 – waldenstrom macroglobulinemia
MeSH C15.378.147.880 – protein c deficiency
MeSH C15.378.147.890 – protein s deficiency

MeSH C15.378.190 – bone marrow diseases

MeSH C15.378.190.196 – anemia, aplastic
MeSH C15.378.190.196.080 – anemia, hypoplastic, congenital
MeSH C15.378.190.196.080.090 – anemia, diamond-blackfan
MeSH C15.378.190.196.080.280 – fanconi anemia
MeSH C15.378.190.250 – bone marrow neoplasms
MeSH C15.378.190.625 – myelodysplastic syndromes
MeSH C15.378.190.625.062 – anemia, refractory
MeSH C15.378.190.625.062.080 – anemia, refractory, with excess of blasts
MeSH C15.378.190.625.070 – anemia, sideroblastic
MeSH C15.378.190.625.460 – hemoglobinuria, paroxysmal
MeSH C15.378.190.625.543 – leukemia, myeloid
MeSH C15.378.190.636 – myeloproliferative disorders
MeSH C15.378.190.636.085 – anemia, myelophthisic
MeSH C15.378.190.636.276 – leukemia, erythroblastic, acute
MeSH C15.378.190.636.484 – leukemoid reaction
MeSH C15.378.190.636.581 – myelofibrosis
MeSH C15.378.190.636.636 – myeloid metaplasia
MeSH C15.378.190.636.753 – polycythemia vera
MeSH C15.378.190.636.860 – thrombocytosis
MeSH C15.378.190.636.860.800 – thrombocythemia, hemorrhagic

MeSH C15.378.400 – hematologic neoplasms

MeSH C15.378.400.200 – bone marrow neoplasms

MeSH C15.378.420 – hemoglobinopathies

MeSH C15.378.420.155 – anemia, sickle cell
MeSH C15.378.420.155.440 – hemoglobin sc disease
MeSH C15.378.420.155.668 – sickle cell trait
MeSH C15.378.420.463 – hemoglobin c disease
MeSH C15.378.420.826 – thalassemia
MeSH C15.378.420.826.100 – alpha-thalassemia
MeSH C15.378.420.826.100.350 – hydrops fetalis
MeSH C15.378.420.826.150 – beta-thalassemia

MeSH C15.378.463 – hemorrhagic disorders

MeSH C15.378.463.067 – afibrinogenemia
MeSH C15.378.463.080 – bernard-soulier syndrome
MeSH C15.378.463.250 – disseminated intravascular coagulation
MeSH C15.378.463.300 – factor v deficiency
MeSH C15.378.463.310 – factor vii deficiency
MeSH C15.378.463.320 – factor x deficiency
MeSH C15.378.463.325 – factor xi deficiency
MeSH C15.378.463.330 – factor xii deficiency
MeSH C15.378.463.335 – factor xiii deficiency
MeSH C15.378.463.500 – hemophilia a
MeSH C15.378.463.510 – hemophilia b
MeSH C15.378.463.550 – hypoprothrombinemias
MeSH C15.378.463.735 – platelet storage pool deficiency
MeSH C15.378.463.735.400 – hermanski-pudlak syndrome
MeSH C15.378.463.740 – purpura, thrombocytopenic, idiopathic
MeSH C15.378.463.810 – thrombasthenia
MeSH C15.378.463.825 – thrombocythemia, hemorrhagic
MeSH C15.378.463.835 – vascular hemostatic disorders
MeSH C15.378.463.835.140 – cryoglobulinemia
MeSH C15.378.463.835.240 – ehlers-danlos syndrome
MeSH C15.378.463.835.385 – hemangioma, cavernous
MeSH C15.378.463.835.385.500 – hemangioma, cavernous, central nervous system
MeSH C15.378.463.835.460 – multiple myeloma
MeSH C15.378.463.835.530 – pseudoxanthoma elasticum
MeSH C15.378.463.835.550 – purpura, hyperglobulinemic
MeSH C15.378.463.835.580 – purpura, schoenlein-henoch
MeSH C15.378.463.835.800 – scurvy
MeSH C15.378.463.835.810 – shwartzman phenomenon
MeSH C15.378.463.835.900 – telangiectasia, hereditary hemorrhagic
MeSH C15.378.463.835.960 – waldenstrom macroglobulinemia
MeSH C15.378.463.841 – vitamin k deficiency
MeSH C15.378.463.841.464 – hemorrhagic disease of newborn
MeSH C15.378.463.920 – von willebrand disease
MeSH C15.378.463.950 – waterhouse-friderichsen syndrome
MeSH C15.378.463.960 – wiskott-aldrich syndrome

MeSH C15.378.553 – leukocyte disorders

MeSH C15.378.553.231 – eosinophilia
MeSH C15.378.553.231.085 – angiolymphoid hyperplasia with eosinophilia
MeSH C15.378.553.231.335 – eosinophilia-myalgia syndrome
MeSH C15.378.553.231.348 – eosinophilic granuloma
MeSH C15.378.553.231.549 – hypereosinophilic syndrome
MeSH C15.378.553.231.549.750 – pulmonary eosinophilia
MeSH C15.378.553.381 – infectious mononucleosis
MeSH C15.378.553.475 – leukocytosis
MeSH C15.378.553.475.428 – leukemoid reaction
MeSH C15.378.553.475.604 – lymphocytosis
MeSH C15.378.553.546 – leukopenia
MeSH C15.378.553.546.184 – agranulocytosis
MeSH C15.378.553.546.184.564 – neutropenia
MeSH C15.378.553.546.605 – lymphopenia
MeSH C15.378.553.546.605.800 – t-lymphocytopenia, idiopathic cd4-positive
MeSH C15.378.553.560 – leukostasis
MeSH C15.378.553.696 – pelger-huet anomaly
MeSH C15.378.553.774 – phagocyte bactericidal dysfunction
MeSH C15.378.553.774.257 – chediak-higashi syndrome
MeSH C15.378.553.774.535 – granulomatous disease, chronic
MeSH C15.378.553.774.600 – job's syndrome

MeSH C15.378.619 – methemoglobinemia

MeSH C15.378.700 – pancytopenia

MeSH C15.378.738 – polycythemia

MeSH C15.378.785 – pregnancy complications, hematologic

MeSH C15.378.800 – preleukemia

MeSH C15.378.896 – sulfhemoglobinemia

MeSH C15.378.925 – thrombophilia

MeSH C15.604 – lymphatic diseases

MeSH C15.604.315 – lymphadenitis

MeSH C15.604.315.249 – cat-scratch disease
MeSH C15.604.315.300 – histiocytic necrotizing lymphadenitis
MeSH C15.604.315.618 – mesenteric lymphadenitis
MeSH C15.604.315.809 – tuberculosis, lymph node

MeSH C15.604.360 – lymphangiectasis

MeSH C15.604.360.500 – lymphangiectasis, intestinal

MeSH C15.604.406 – lymphangitis

MeSH C15.604.451 – lymphatic abnormalities

MeSH C15.604.451.500 – lymphangiectasis, intestinal

MeSH C15.604.496 – lymphedema

MeSH C15.604.496.320 – elephantiasis
MeSH C15.604.496.320.350 – elephantiasis, filarial

MeSH C15.604.510 – lymphocele

MeSH C15.604.515 – lymphoproliferative disorders

MeSH C15.604.515.032 – agammaglobulinemia
MeSH C15.604.515.245 – giant lymph node hyperplasia
MeSH C15.604.515.292 – granuloma
MeSH C15.604.515.292.007 – angiolymphoid hyperplasia with eosinophilia
MeSH C15.604.515.292.015 – Churg–Strauss syndrome
MeSH C15.604.515.435 – heavy chain disease
MeSH C15.604.515.435.512 – immunoproliferative small intestinal disease
MeSH C15.604.515.509 – immunoblastic lymphadenopathy
MeSH C15.604.515.516 – infectious mononucleosis
MeSH C15.604.515.553 – leukemia, hairy cell
MeSH C15.604.515.560 – leukemia, lymphocytic
MeSH C15.604.515.561 – leukemia, myeloid
MeSH C15.604.515.561.550 – leukemia, nonlymphocytic, acute
MeSH C15.604.515.561.550.512 – leukemia, myelocytic, acute
MeSH C15.604.515.562 – lymphangiomyoma
MeSH C15.604.515.562.465 – lymphangioleiomyomatosis
MeSH C15.604.515.569 – lymphoma
MeSH C15.604.515.569.355 – hodgkin disease
MeSH C15.604.515.569.480 – lymphoma, non-hodgkin
MeSH C15.604.515.569.480.150 – lymphoma, b-cell
MeSH C15.604.515.569.480.150.165 – burkitt lymphoma
MeSH C15.604.515.569.480.150.450 – lymphoma, aids-related
MeSH C15.604.515.569.480.150.570 – lymphoma, mucosa-associated lymphoid tissue
MeSH C15.604.515.569.480.150.700 – lymphoma, small-cell
MeSH C15.604.515.569.480.300 – lymphoma, diffuse
MeSH C15.604.515.569.480.300.300 – lymphoma, large-cell, diffuse
MeSH C15.604.515.569.480.300.450 – lymphoma, large-cell, immunoblastic
MeSH C15.604.515.569.480.300.475 – lymphoma, lymphoblastic
MeSH C15.604.515.569.480.300.500 – lymphoma, mixed-cell, diffuse
MeSH C15.604.515.569.480.300.725 – lymphoma, small cleaved-cell, diffuse
MeSH C15.604.515.569.480.300.725.500 – lymphoma, mantle-cell
MeSH C15.604.515.569.480.300.750 – lymphoma, small lymphocytic
MeSH C15.604.515.569.480.300.775 – lymphoma, small noncleaved-cell
MeSH C15.604.515.569.480.350 – lymphoma, follicular
MeSH C15.604.515.569.480.350.350 – lymphoma, large-cell, follicular
MeSH C15.604.515.569.480.350.525 – lymphoma, mixed-cell, follicular
MeSH C15.604.515.569.480.350.750 – lymphoma, small cleaved-cell, follicular
MeSH C15.604.515.569.480.425 – lymphoma, high-grade
MeSH C15.604.515.569.480.425.450 – lymphoma, large-cell, immunoblastic
MeSH C15.604.515.569.480.425.475 – lymphoma, lymphoblastic
MeSH C15.604.515.569.480.425.775 – lymphoma, small noncleaved-cell
MeSH C15.604.515.569.480.425.775.165 – burkitt lymphoma
MeSH C15.604.515.569.480.450 – lymphoma, intermediate-grade
MeSH C15.604.515.569.480.450.300 – lymphoma, large-cell, diffuse
MeSH C15.604.515.569.480.450.350 – lymphoma, large-cell, follicular
MeSH C15.604.515.569.480.450.500 – lymphoma, mixed-cell, diffuse
MeSH C15.604.515.569.480.450.725 – lymphoma, small cleaved-cell, diffuse
MeSH C15.604.515.569.480.450.725.500 – lymphoma, mantle-cell
MeSH C15.604.515.569.480.475 – lymphoma, large-cell
MeSH C15.604.515.569.480.475.300 – lymphoma, large-cell, diffuse
MeSH C15.604.515.569.480.475.350 – lymphoma, large-cell, follicular
MeSH C15.604.515.569.480.475.450 – lymphoma, large-cell, immunoblastic
MeSH C15.604.515.569.480.475.465 – lymphoma, large-cell, ki-1
MeSH C15.604.515.569.480.475.475 – lymphoma, lymphoblastic
MeSH C15.604.515.569.480.500 – lymphoma, low-grade
MeSH C15.604.515.569.480.500.525 – lymphoma, mixed-cell, follicular
MeSH C15.604.515.569.480.500.570 – lymphoma, mucosa-associated lymphoid tissue
MeSH C15.604.515.569.480.500.750 – lymphoma, small cleaved-cell, follicular
MeSH C15.604.515.569.480.500.770 – lymphoma, small lymphocytic
MeSH C15.604.515.569.480.550 – lymphoma, mixed-cell
MeSH C15.604.515.569.480.550.500 – lymphoma, mixed-cell, diffuse
MeSH C15.604.515.569.480.550.525 – lymphoma, mixed-cell, follicular
MeSH C15.604.515.569.480.700 – lymphoma, small-cell
MeSH C15.604.515.569.480.700.725 – lymphoma, small cleaved-cell, diffuse
MeSH C15.604.515.569.480.700.725.500 – lymphoma, mantle-cell
MeSH C15.604.515.569.480.700.730 – lymphoma, small cleaved-cell, follicular
MeSH C15.604.515.569.480.700.750 – lymphoma, small lymphocytic
MeSH C15.604.515.569.480.700.775 – lymphoma, small noncleaved-cell
MeSH C15.604.515.569.480.750 – lymphoma, t-cell
MeSH C15.604.515.569.480.750.475 – lymphoma, lymphoblastic
MeSH C15.604.515.569.480.750.800 – lymphoma, t-cell, cutaneous
MeSH C15.604.515.569.480.750.800.465 – lymphoma, large-cell, ki-1
MeSH C15.604.515.569.480.750.800.550 – mycosis fungoides
MeSH C15.604.515.569.480.750.800.775 – sezary syndrome
MeSH C15.604.515.569.480.750.825 – lymphoma, t-cell, peripheral
MeSH C15.604.515.569.480.875 – lymphoma, undifferentiated
MeSH C15.604.515.569.480.875.300 – lymphoma, large-cell, diffuse
MeSH C15.604.515.569.480.875.775 – lymphoma, small noncleaved-cell
MeSH C15.604.515.569.480.875.775.165 – burkitt lymphoma
MeSH C15.604.515.571 – lymphomatoid granulomatosis
MeSH C15.604.515.700 – marek disease
MeSH C15.604.515.827 – sarcoidosis
MeSH C15.604.515.827.725 – sarcoidosis, pulmonary
MeSH C15.604.515.827.865 – uveoparotid fever
MeSH C15.604.515.841 – sezary syndrome
MeSH C15.604.515.880 – tumor lysis syndrome
MeSH C15.604.515.925 – waldenstrom macroglobulinemia

MeSH C15.604.560 – mucocutaneous lymph node syndrome

MeSH C15.604.613 – pseudolymphoma

MeSH C15.604.667 – reticuloendotheliosis

MeSH C15.604.667.358 – gaucher disease
MeSH C15.604.667.400 – histiocytosis
MeSH C15.604.667.400.390 – histiocytic disorders, malignant
MeSH C15.604.667.400.390.400 – histiocytosis, malignant
MeSH C15.604.667.400.390.500 – leukemia, monocytic, acute
MeSH C15.604.667.400.390.550 – lymphoma, large-cell
MeSH C15.604.667.400.390.550.465 – lymphoma, large-cell, ki-1
MeSH C15.604.667.400.400 – histiocytosis, langerhans-cell
MeSH C15.604.667.400.400.360 – eosinophilic granuloma
MeSH C15.604.667.400.410 – histiocytosis, non-langerhans-cell
MeSH C15.604.667.400.410.224 – erdheim-chester disease
MeSH C15.604.667.400.410.450 – histiocytosis, sinus
MeSH C15.604.667.400.410.575 – lymphohistiocytosis, hemophagocytic
MeSH C15.604.667.400.410.625 – niemann-pick diseases
MeSH C15.604.667.400.410.800 – sea-blue histiocyte syndrome
MeSH C15.604.667.400.410.900 – xanthogranuloma, juvenile
MeSH C15.604.667.750 – mast-cell sarcoma

MeSH C15.604.744 – splenic diseases

MeSH C15.604.744.293 – hypersplenism
MeSH C15.604.744.428 – myeloid metaplasia
MeSH C15.604.744.617 – splenic infarction
MeSH C15.604.744.680 – splenic neoplasms
MeSH C15.604.744.742 – splenic rupture
MeSH C15.604.744.742.500 – splenosis
MeSH C15.604.744.909 – tuberculosis, splenic
MeSH C15.604.744.954 – wandering spleen

MeSH C15.604.816 – thymus hyperplasia

MeSH C15.604.861 – thymus neoplasms

MeSH C15.604.921 – tuberculosis, lymph node

MeSH C15.604.921.500 – king's evil

The list continues at List of MeSH codes (C16).

Lists of MeSH codes

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