List of MeSH codes (C15)

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   C15.378.925 – thrombophilia

• MeSH   C15.378.925.050 – activated protein c resistance
• MeSH   C15.378.925.075 – antithrombin iii deficiency
• MeSH   C15.378.925.220 – disseminated intravascular coagulation
• MeSH   C15.378.925.795 – protein c deficiency
• MeSH   C15.378.925.800 – protein s deficiency
• MeSH   C15.378.925.850 – purpura, thrombotic thrombocytopenic

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   C15.604.451 – 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   C15.604.515 – 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   C15.604.667 – 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   C15.604.921 – tuberculosis, lymph node

• MeSH   C15.604.921.500 – king's evil

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