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. (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
hematologic diseases
MeSH C15.378.071 – anemia
- anemia, aplastic
- anemia, hypoplastic, congenital
- anemia, diamond-blackfan
- anemia, hemolytic
- anemia, hemolytic, autoimmune
- anemia, sickle cell
- elliptocytosis, hereditary
- glucosephosphate dehydrogenase deficiency
- favism
- hemoglobin c disease
- spherocytosis, hereditary
- beta-thalassemia
- favism
- hemolytic-uremic syndrome
- anemia, hypochromic
- anemia, iron-deficiency
- anemia, macrocytic
- anemia, megaloblastic
- anemia, pernicious
- anemia, myelophthisic
- MeSH C15.378.071.363 – anemia, neonatal
- fetofetal transfusion
- anemia, refractory
- anemia, refractory, with excess of blasts
- anemia, sideroblastic
- red-cell aplasia, pure
- anemia, diamond-blackfan
blood coagulation disorders
- coagulation protein disorders
- activated protein c resistance
- afibrinogenemia
- factor v deficiency
- factor vii deficiency
- factor x deficiency
- factor xi deficiency
- factor xii deficiency
- factor xiii deficiency
- hemophilia a
- hemophilia b
- hypoprothrombinemias
- von willebrand disease
- activated protein c resistance
- afibrinogenemia
- antithrombin iii deficiency
- bernard-soulier syndrome
- factor v deficiency
- factor vii deficiency
- factor x deficiency
- factor xi deficiency
- factor xii deficiency
- factor xiii deficiency
- hemophilia a
- hemophilia b
- hermanski-pudlak syndrome
- hypoprothrombinemias
- protein c deficiency
- thrombasthenia
- von willebrand disease
- wiskott-aldrich syndrome
- hermanski-pudlak syndrome
- protein s deficiency
- MeSH C15.378.100.802 – purpura
- purpura, hyperglobulinemic
- purpura, schoenlein-henoch
- purpura, thrombocytopenic
- purpura, thrombocytopenic
- purpura, thrombocytopenic, idiopathic
- purpura, thrombotic thrombocytopenic
- wiskott-aldrich syndrome
- vitamin k deficiency
- hemorrhagic disease of newborn
- erythroblastosis, fetal
- MeSH C15.378.120.413.502 – kernicterus
- rh isoimmunization
blood platelet disorders
- bernard-soulier syndrome
- hermanski-pudlak syndrome
- thrombasthenia
- MeSH C15.378.140.855 – thrombocytopenia
- hemolytic-uremic syndrome
- purpura, thrombocytopenic
- purpura, thrombocytopenic, idiopathic
- purpura, thrombotic thrombocytopenic
- wiskott-aldrich syndrome
- thrombocytosis
- von willebrand disease
blood protein disorders
- agammaglobulinemia
- antithrombin iii deficiency
- iga deficiency
- igg deficiency
- monoclonal gammopathies, benign
- MeSH C15.378.147.607 – hypoproteinemia
- paraproteinemias
- immunoproliferative small intestinal disease
- poems syndrome
- waldenstrom macroglobulinemia
- protein c deficiency
- protein s deficiency
bone marrow diseases
- anemia, aplastic
- anemia, hypoplastic, congenital
- anemia, diamond-blackfan
- bone marrow neoplasms
- myelodysplastic syndromes
- anemia, refractory
- anemia, refractory, with excess of blasts
- anemia, sideroblastic
- MeSH C15.378.190.625.460– hemoglobinuria, paroxysmal
- leukemia, myeloid
- myeloproliferative disorders
- anemia, myelophthisic
- leukemia, erythroblastic, acute
- myelofibrosis
- myeloid metaplasia
- thrombocytosis
hematologic neoplasms
- bone marrow neoplasms
hemoglobinopathies
- anemia, sickle cell
- hemoglobin c disease
- MeSH C15.378.420.826 – thalassemia
- beta-thalassemia
hemorrhagic disorders
- afibrinogenemia
- bernard-soulier syndrome
- factor v deficiency
- factor vii deficiency
- factor x deficiency
- factor xi deficiency
- factor xii deficiency
- factor xiii deficiency
- hemophilia a
- hemophilia b
- hypoprothrombinemias
- hermanski-pudlak syndrome
- purpura, thrombocytopenic, idiopathic
- thrombasthenia
- vascular hemostatic disorders
- ehlers-danlos syndrome
- hemangioma, cavernous
- hemangioma, cavernous, central nervous system
- purpura, hyperglobulinemic
- purpura, schoenlein-henoch
- MeSH C15.378.463.835.800 – scurvy
- telangiectasia, hereditary hemorrhagic
- waldenstrom macroglobulinemia
- vitamin k deficiency
- hemorrhagic disease of newborn
- von willebrand disease
- waterhouse-friderichsen syndrome
- wiskott-aldrich syndrome
leukocyte disorders
- MeSH C15.378.553.231 – eosinophilia
- eosinophilia-myalgia syndrome
- pulmonary eosinophilia
- MeSH C15.378.553.475 – leukocytosis
- MeSH C15.378.553.475.604 – lymphocytosis
- MeSH C15.378.553.546 – leukopenia
- lymphopenia
- MeSH C15.378.553.560 – leukostasis
- pelger-huet anomaly
- chediak-higashi syndrome
- granulomatous disease, chronic
- job's syndrome
MeSH C15.378.619 – methemoglobinemia
MeSH C15.378.700 – pancytopenia
MeSH C15.378.738 – polycythemia
pregnancy complications, hematologic
preleukemia
MeSH C15.378.896 – sulfhemoglobinemia
MeSH C15.378.925 – thrombophilia
- activated protein c resistance
- antithrombin iii deficiency
- protein c deficiency
- protein s deficiency
- purpura, thrombotic thrombocytopenic
lymphatic diseases
lymphadenitis
- histiocytic necrotizing lymphadenitis
- mesenteric lymphadenitis
lymphangiectasis
MeSH C15.604.406 – lymphangitis
MeSH C15.604.496 – lymphedema
- MeSH C15.604.496.320 – elephantiasis
MeSH C15.604.510 – lymphocele
- agammaglobulinemia
- MeSH C15.604.515.292 – granuloma
- Churg–Strauss syndrome
- immunoproliferative small intestinal disease
- immunoblastic lymphadenopathy
- leukemia, hairy cell
- leukemia, lymphocytic
- leukemia, myeloid
- leukemia, myelocytic, acute
- MeSH C15.604.515.562 – lymphangiomyoma
- MeSH C15.604.515.569 – lymphoma
- hodgkin disease
- lymphoma, non-hodgkin
- lymphoma, b-cell
- lymphoma, aids-related
- lymphoma, mucosa-associated lymphoid tissue
- lymphoma, small-cell
- lymphoma, diffuse
- lymphoma, large-cell, diffuse
- lymphoma, large-cell, immunoblastic
- lymphoma, lymphoblastic
- lymphoma, small cleaved-cell, diffuse
- lymphoma, mantle-cell
- lymphoma, follicular
- lymphoma, large-cell, follicular
- lymphoma, small cleaved-cell, follicular
- lymphoma, high-grade
- lymphoma, large-cell, immunoblastic
- lymphoma, lymphoblastic
- lymphoma, intermediate-grade
- lymphoma, large-cell, diffuse
- lymphoma, large-cell, follicular
- lymphoma, small cleaved-cell, diffuse
- lymphoma, mantle-cell
- lymphoma, large-cell
- lymphoma, large-cell, diffuse
- lymphoma, large-cell, follicular
- lymphoma, large-cell, immunoblastic
- lymphoma, large-cell, ki-1
- lymphoma, lymphoblastic
- lymphoma, low-grade
- lymphoma, mucosa-associated lymphoid tissue
- lymphoma, small cleaved-cell, follicular
- lymphoma, small-cell
- lymphoma, small cleaved-cell, diffuse
- lymphoma, mantle-cell
- lymphoma, small cleaved-cell, follicular
- lymphoma, t-cell
- lymphoma, lymphoblastic
- lymphoma, t-cell, cutaneous
- lymphoma, large-cell, ki-1
- sezary syndrome
- lymphoma, t-cell, peripheral
- lymphoma, large-cell, diffuse
- marek disease
- MeSH C15.604.515.827 – sarcoidosis
- sarcoidosis, pulmonary
- uveoparotid fever
- sezary syndrome
- waldenstrom macroglobulinemia
mucocutaneous lymph node syndrome
MeSH C15.604.613 – pseudolymphoma
reticuloendotheliosis
- gaucher disease
- MeSH C15.604.667.400 – histiocytosis
- histiocytosis, malignant
- leukemia, monocytic, acute
- lymphoma, large-cell
- lymphoma, large-cell, ki-1
- histiocytosis, langerhans-cell
- histiocytosis, non-langerhans-cell
- erdheim-chester disease
- lymphohistiocytosis, hemophagocytic
- niemann-pick diseases
- sea-blue histiocyte syndrome
- xanthogranuloma, juvenile
- mast-cell sarcoma
splenic diseases
- hypersplenism
- myeloid metaplasia
- MeSH C15.604.744.680 – splenic neoplasms
- splenic rupture
- MeSH C15.604.744.742.500 – splenosis
- MeSH C15.604.744.954 – wandering spleen
MeSH C15.604.816 – thymus hyperplasia
thymus neoplasms
- king's evil
The list continues at List of MeSH codes (C16).