more general categories |
information about this item |
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1. Human Genes |
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1. Human Genes |
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nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha [HGNC:NFKBIA] (290) |
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jun proto-oncogene [HGNC:JUN] (290) |
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integrin, alpha M (complement component 3 receptor 3 subunit) [HGNC:ITGAM] (75) |
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intercellular adhesion molecule 1 [HGNC:ICAM1] (286) |
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macrophage scavenger receptor 1 [HGNC:MSR1] (27) |
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vascular cell adhesion molecule 1 [HGNC:VCAM1] (172) |
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chemokine (C-C motif) ligand 02 [HGNC:CCL2] (337) |
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chemokine (C-C motif) ligand 05 [HGNC:CCL5] (141) |
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chemokine (C-C motif) ligand 07 [HGNC:CCL7] (18) |
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chemokine (C-C motif) ligand 11 [HGNC:CCL11] (38) |
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integrin, alpha M (complement component 3 receptor 3 subunit) [HGNC:ITGAM] (75) |
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oxidized low density lipoprotein (lectin-like) receptor 1 [HGNC:OLR1] (40) |
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cytochrome b-245, beta polypeptide [HGNC:CYBB] (27) |
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chemokine (C-C motif) ligand 02 [HGNC:CCL2] (337) |
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chemokine (C-C motif) ligand 05 [HGNC:CCL5] (141) |
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chemokine (C-C motif) ligand 07 [HGNC:CCL7] (18) |
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chemokine (C-C motif) ligand 11 [HGNC:CCL11] (38) |
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chemokine (C-X-C motif) ligand 01 (melanoma growth stimulating activity, alpha) [HGNC:CXCL1] (82) |
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chemokine (C-X-C motif) ligand 10 [HGNC:CXCL10] (81) |
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interleukin 08 [HGNC:IL8] (649) |
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fibronectin 1 [HGNC:FN1] (112) |
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vascular cell adhesion molecule 1 [HGNC:VCAM1] (172) |
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vascular cell adhesion molecule 1 [HGNC:VCAM1] (172) |
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intercellular adhesion molecule 1 [HGNC:ICAM1] (286) |
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vascular cell adhesion molecule 1 [HGNC:VCAM1] (172) |
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integrin, alpha M (complement component 3 receptor 3 subunit) [HGNC:ITGAM] (75) |
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interferon, beta 1, fibroblast [HGNC:IFNB1] (14) |
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interleukin 06 (interferon, beta 2) [HGNC:IL6] (511) |
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interleukin 01, beta [HGNC:IL1B] (497) |
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interleukin 06 (interferon, beta 2) [HGNC:IL6] (511) |
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interleukin 08 [HGNC:IL8] (649) |
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E1A binding protein p300 [HGNC:EP300] (48) |
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mitogen-activated protein kinase 01 [HGNC:MAPK1] (651) |
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mitogen-activated protein kinase 03 [HGNC:MAPK3] (644) |
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mitogen-activated protein kinase 08 [HGNC:MAPK8] (234) |
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mitogen-activated protein kinase 09 [HGNC:MAPK9] (121) |
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HtrA serine peptidase 2 [HGNC:HTRA2] (29) |
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HtrA serine peptidase 2 [HGNC:HTRA2] (29) |
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serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1 [HGNC:SERPINE1] (138) |
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Janus kinase 2 [HGNC:JAK2] (44) |
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signal transducer and activator of transcription 1, 91kDa [HGNC:STAT1] (108) |
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tumor necrosis factor [HGNC:TNF] (795) |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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binding (2423) |
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cotreatment (1499) |
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localization (731) |
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expression (2187) |
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reaction (3393) |
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response to substance (713) |
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abundance (630) |
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activity (2865) |
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expression (3238) |
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phosphorylation (1060) |
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reaction (1574) |
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secretion (901) |
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4. Semantic Terms |
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4. Semantic Terms |
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Pharmacologic Substance [STY:T121] (11019) |
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Organic Chemical [STY:T109] (44144) |
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A. Anatomy |
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A. Anatomy |
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Allanson Pantzar McLeod syndrome [MESH:C537048] (503) |
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Chromosome 17 deletion [MESH:C538045] (769) |
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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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Chlamydia Infections [MESH:D002690] (1696) |
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Salmonella Infections, Animal [MESH:D012481] (604) |
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Legionnaires' Disease [MESH:D007877] (611) |
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Mycoplasma Infections [MESH:D009175] (1947) |
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Listeriosis [MESH:D008088] (1622) |
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Staphylococcal Infections [MESH:D013203] (264) |
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Mycobacterium Infections, Nontuberculous [MESH:D009165] (480) |
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Tuberculosis, Pulmonary [MESH:D014397] (678) |
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Chlamydia Infections [MESH:D002690] (1693) |
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Arthritis, Infectious [MESH:D001170] (1702) |
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Respiratory Tract Infections [MESH:D012141] (199) |
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Urinary Tract Infections [MESH:D014552] (984) |
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Appendicitis [MESH:D001064] (774) |
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Peritonitis [MESH:D010538] (800) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Shock, Septic [MESH:D012772] (1830) |
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Endotoxemia [MESH:D019446] (1289) |
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Chlamydia Infections [MESH:D002690] (1693) |
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Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
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Endotoxemia [MESH:D019446] (1289) |
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Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
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Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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Meningitis, Aseptic [MESH:D008582] (1305) |
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Hepatitis B [MESH:D006509] (976) |
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Cytomegalovirus Infections [MESH:D003586] (222) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Hepatitis B [MESH:D006509] (976) |
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Hepatitis C [MESH:D006526] (1627) |
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Meningitis, Aseptic [MESH:D008582] (1305) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Hepatitis C [MESH:D006526] (1627) |
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Respiratory Syncytial Virus Infections [MESH:D018357] (852) |
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Influenza, Human [MESH:D007251] (1075) |
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Cardiovirus Infections [MESH:D018188] (1548) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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C03. Parasitic Diseases |
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C03. Parasitic Diseases |
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Liver Diseases, Parasitic [MESH:D008109] (1009) |
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Trichuriasis [MESH:D014257] (805) |
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Schistosomiasis mansoni [MESH:D012555] (1033) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Malaria [MESH:D008288] (2175) |
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Entamoebiasis [MESH:D004749] (1689) |
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Leishmaniasis, Visceral [MESH:D007898] (2149) |
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Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
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Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
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C04. Neoplasms |
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C04. Neoplasms |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344) |
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Leukemia, Promyelocytic, Acute [MESH:D015473] (1367) |
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Hodgkin Disease [MESH:D006689] (1082) |
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Lymphoma, Follicular [MESH:D008224] (1025) |
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Lymphoma, AIDS-Related [MESH:D016483] (278) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) |
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Hepatoblastoma [MESH:D018197] (548) |
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Sarcoma, Synovial [MESH:D013584] (993) |
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Chondrosarcoma, Mesenchymal [MESH:D018211] (1161) |
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Mastocytosis, Systemic [MESH:D034721] (769) |
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Osteosarcoma [MESH:D012516] (2175) |
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Fibromatosis, Aggressive [MESH:D018222] (1562) |
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Leiomyosarcoma [MESH:D007890] (977) |
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Rhabdomyoma [MESH:D012207] (200) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Leiomyosarcoma [MESH:D007890] (977) |
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Osteosarcoma [MESH:D012516] (2175) |
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Sarcoma, Synovial [MESH:D013584] (993) |
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Chondrosarcoma, Mesenchymal [MESH:D018211] (1161) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Medulloblastoma [MESH:D008527] (1282) |
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Glioblastoma [MESH:D005909] (2554) |
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Medulloblastoma [MESH:D008527] (1282) |
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Neuroblastoma [MESH:D009447] (1420) |
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Melanoma, Amelanotic [MESH:D018328] (65) |
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Melanoma, Experimental [MESH:D008546] (210) |
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Adenoma, Oxyphilic [MESH:D018249] (115) |
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Mesothelioma [MESH:D008654] (2567) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Carcinoma, Basal Cell [MESH:D002280] (1628) |
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Carcinoma in Situ [MESH:D002278] (2111) |
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Carcinoma, Small Cell [MESH:D018288] (1317) |
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Carcinoma, Transitional Cell [MESH:D002295] (2662) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Adenocarcinoma, Clear Cell [MESH:D018262] (1291) |
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Carcinoma, Adenoid Cystic [MESH:D003528] (1561) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Cholangiocarcinoma [MESH:D018281] (2398) |
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Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Carcinoma, Basal Cell [MESH:D002280] (1628) |
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Carcinoma, Intraductal, Noninfiltrating [MESH:D002285] (500) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Mesothelioma [MESH:D008654] (2567) |
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Medulloblastoma [MESH:D008527] (1282) |
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Glioblastoma [MESH:D005909] (2554) |
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Medulloblastoma [MESH:D008527] (1282) |
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Neuroblastoma [MESH:D009447] (1420) |
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Papilloma [MESH:D010212] (2243) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Medulloblastoma [MESH:D008527] (1282) |
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Glioblastoma [MESH:D005909] (2554) |
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Medulloblastoma [MESH:D008527] (1282) |
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Neuroblastoma [MESH:D009447] (1420) |
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Melanoma, Amelanotic [MESH:D018328] (65) |
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Melanoma, Experimental [MESH:D008546] (210) |
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Multiple Myeloma [MESH:D009101] (2767) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Hemangioblastoma [MESH:D018325] (395) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Melanoma, Amelanotic [MESH:D018328] (65) |
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Melanoma, Experimental [MESH:D008546] (210) |
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Bone Neoplasms [MESH:D001859] (1334) |
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Skin Neoplasms [MESH:D012878] (2992) |
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Soft Tissue Neoplasms [MESH:D012983] (2003) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Gallbladder Neoplasms [MESH:D005706] (993) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Anus Neoplasms [MESH:D001005] (69) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769) |
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Thyroid cancer, anaplastic [MESH:C536910] (489) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Leukoplakia, Oral [MESH:D007972] (921) |
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Tongue Neoplasms [MESH:D014062] (1518) |
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Nasopharyngeal carcinoma [MESH:C538339] (1198) |
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Thyroid cancer, anaplastic [MESH:C536910] (489) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Papilloma, Choroid Plexus [MESH:D020288] (769) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Small Cell Lung Carcinoma [MESH:D055752] (1380) |
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Endometrial Neoplasms [MESH:D016889] (1987) |
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Penile Neoplasms [MESH:D010412] (890) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Melanoma, Experimental [MESH:D008546] (210) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Anaplasia [MESH:D000708] (348) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Recurrence, Local [MESH:D009364] (1949) |
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Neoplasm, Residual [MESH:D018365] (478) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Lymphatic Metastasis [MESH:D008207] (917) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Li-Fraumeni Syndrome [MESH:D016864] (859) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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ACTH Syndrome, Ectopic [MESH:D000182] (200) |
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Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
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Leukoplakia, Oral [MESH:D007972] (921) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Cartilage Diseases [MESH:D002357] (438) |
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Bone Neoplasms [MESH:D001859] (1334) |
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Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
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Spondyloepimetaphyseal Dysplasia, Missouri Type [MESH:C566574] (142) |
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Osteogenesis imperfecta, type 2A [MESH:C536042] (375) |
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Osteogenesis imperfecta, type 3 [MESH:C536044] (375) |
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Osteogenesis imperfecta, type 4 [MESH:C536045] (375) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Osteolysis [MESH:D010014] (1787) |
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Femur Head Necrosis [MESH:D005271] (268) |
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Kyphosis [MESH:D007738] (637) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34) |
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Cleft Palate [MESH:D002972] (1330) |
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Synovitis [MESH:D013585] (270) |
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Arthritis, Experimental [MESH:D001169] (3142) |
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Arthritis, Infectious [MESH:D001170] (1702) |
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Arthritis, Juvenile [MESH:D001171] (1060) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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Chondrocalcinosis [MESH:D002805] (213) |
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Osteoarthritis [MESH:D010003] (1743) |
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Sacroiliitis [MESH:D058566] (202) |
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Arthritis, Gouty [MESH:D015210] (211) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Muscle Weakness [MESH:D018908] (478) |
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MELAS Syndrome [MESH:D017241] (1061) |
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MERRF Syndrome [MESH:D017243] (1053) |
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Kearns-Sayre Syndrome [MESH:D007625] (1054) |
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Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
|
|
|
Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
|
|
|
|
|
|
Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Osteoarthritis [MESH:D010003] (1743) |
|
|
Arthritis, Gouty [MESH:D015210] (211) |
|
|
C06. Digestive System Diseases |
|
|
|
C06. Digestive System Diseases |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
Gallbladder Neoplasms [MESH:D005706] (993) |
|
|
Gallbladder Neoplasms [MESH:D005706] (993) |
|
|
Barrett Esophagus [MESH:D001471] (1930) |
|
|
Pancreatic Neoplasms [MESH:D010190] (3820) |
|
|
Gallbladder Neoplasms [MESH:D005706] (993) |
|
|
Stomach Neoplasms [MESH:D013274] (4942) |
|
|
Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
|
|
Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
|
|
|
|
|
|
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Anus Neoplasms [MESH:D001005] (69) |
|
|
Carcinoma, Hepatocellular [MESH:D006528] (5375) |
|
|
Liver Neoplasms, Experimental [MESH:D008114] (2837) |
|
|
|
|
|
Barrett Esophagus [MESH:D001471] (1930) |
|
|
Esophageal Stenosis [MESH:D004940] (490) |
|
|
|
|
|
Gastroesophageal Reflux [MESH:D005764] (1465) |
|
|
Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
|
|
Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
|
|
Esophagitis, Peptic [MESH:D004942] (709) |
|
|
Appendicitis [MESH:D001064] (774) |
|
|
Mucositis [MESH:D052016] (1238) |
|
|
Colitis, Ulcerative [MESH:D003093] (2601) |
|
|
Ileitis [MESH:D007079] (137) |
|
|
Enterocolitis, Necrotizing [MESH:D020345] (1367) |
|
|
Esophagitis, Peptic [MESH:D004942] (709) |
|
|
Gastritis, Atrophic [MESH:D005757] (947) |
|
|
Colitis, Ulcerative [MESH:D003093] (2601) |
|
|
Crohn Disease [MESH:D003424] (2585) |
|
|
Peptic Ulcer Hemorrhage [MESH:D010438] (553) |
|
|
Stomach Neoplasms [MESH:D013274] (4942) |
|
|
Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
|
|
Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
|
|
|
|
|
|
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Anus Neoplasms [MESH:D001005] (69) |
|
|
Intestinal Perforation [MESH:D007416] (471) |
|
|
Mesenteric Vascular Occlusion [MESH:D008641] (147) |
|
|
Appendicitis [MESH:D001064] (774) |
|
|
|
|
|
Colitis, Ulcerative [MESH:D003093] (2601) |
|
|
|
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
|
|
|
Duodenal Ulcer [MESH:D004381] (1549) |
|
|
Ileitis [MESH:D007079] (137) |
|
|
Enterocolitis, Necrotizing [MESH:D020345] (1367) |
|
|
Ileitis [MESH:D007079] (137) |
|
|
Colitis, Ulcerative [MESH:D003093] (2601) |
|
|
Crohn Disease [MESH:D003424] (2585) |
|
|
|
|
|
|
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Anus Neoplasms [MESH:D001005] (69) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
|
|
|
Anus Neoplasms [MESH:D001005] (69) |
|
|
|
|
|
Anus Neoplasms [MESH:D001005] (69) |
|
|
Duodenal Ulcer [MESH:D004381] (1549) |
|
|
Esophagitis, Peptic [MESH:D004942] (709) |
|
|
Stomach Ulcer [MESH:D013276] (2915) |
|
|
Gastroparesis [MESH:D018589] (732) |
|
|
Stomach Neoplasms [MESH:D013274] (4942) |
|
|
Gastritis, Atrophic [MESH:D005757] (947) |
|
|
Stomach Ulcer [MESH:D013276] (2915) |
|
|
Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135) |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Budd-Chiari Syndrome [MESH:D006502] (164) |
|
|
Hepatomegaly [MESH:D006529] (1169) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hypertension, Portal [MESH:D006975] (869) |
|
|
Liver Diseases, Parasitic [MESH:D008109] (1009) |
|
|
Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567) |
|
|
Fatty Liver, Alcoholic [MESH:D005235] (657) |
|
|
|
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
Liver Failure, Acute [MESH:D017114] (2404) |
|
|
Hepatitis, Alcoholic [MESH:D006519] (1613) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
Hepatitis B [MESH:D006509] (976) |
|
|
Hepatitis C [MESH:D006526] (1627) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
|
|
Fatty Liver, Alcoholic [MESH:D005235] (657) |
|
|
Hepatitis, Alcoholic [MESH:D006519] (1613) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Carcinoma, Hepatocellular [MESH:D006528] (5375) |
|
|
Liver Neoplasms, Experimental [MESH:D008114] (2837) |
|
|
Pancreatic Neoplasms [MESH:D010190] (3820) |
|
|
Pancreatitis [MESH:D010195] (1924) |
|
|
Mesenteric Vascular Occlusion [MESH:D008641] (147) |
|
|
Peritonitis [MESH:D010538] (800) |
|
|
C07. Stomatognathic Diseases |
|
|
|
C07. Stomatognathic Diseases |
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Facial Paralysis [MESH:D005158] (238) |
|
|
Mucositis [MESH:D052016] (1238) |
|
|
Oral Submucous Fibrosis [MESH:D009914] (2432) |
|
|
Oral Ulcer [MESH:D019226] (488) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Leukoplakia, Oral [MESH:D007972] (921) |
|
|
Tongue Neoplasms [MESH:D014062] (1518) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
Tongue Neoplasms [MESH:D014062] (1518) |
|
|
|
|
|
|
|
|
Nasopharyngeal carcinoma [MESH:C538339] (1198) |
|
|
|
|
|
Nasopharyngeal carcinoma [MESH:C538339] (1198) |
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
C08. Respiratory Tract Diseases |
|
|
|
C08. Respiratory Tract Diseases |
|
|
Not Fully Specified [NFS] (1984) |
|
|
Granuloma, Respiratory Tract [MESH:D015769] (502) |
|
|
Bronchial Hyperreactivity [MESH:D016535] (1357) |
|
|
Bronchiectasis [MESH:D001987] (1792) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
|
|
|
Bronchiolitis Obliterans [MESH:D001989] (611) |
|
|
Hypertension, Pulmonary [MESH:D006976] (2000) |
|
|
Pulmonary Edema [MESH:D011654] (2109) |
|
|
Pulmonary Embolism [MESH:D011655] (1118) |
|
|
Pulmonary Fibrosis [MESH:D011658] (3140) |
|
|
Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
|
|
Tuberculosis, Pulmonary [MESH:D014397] (678) |
|
|
Alveolitis, Extrinsic Allergic [MESH:D000542] (496) |
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Asbestosis [MESH:D001195] (935) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
Silicosis [MESH:D012829] (1273) |
|
|
Asthma [MESH:D001249] (3903) |
|
|
|
|
|
Bronchiolitis Obliterans [MESH:D001989] (611) |
|
|
Pulmonary Emphysema [MESH:D011656] (1259) |
|
|
Acute Lung Injury [MESH:D055371] (1907) |
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Asbestosis [MESH:D001195] (935) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
Silicosis [MESH:D012829] (1273) |
|
|
Bronchopulmonary Dysplasia [MESH:D001997] (1021) |
|
|
Adenocarcinoma of lung [MESH:C538231] (1487) |
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
|
Pneumonia, Aspiration [MESH:D011015] (824) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
|
|
Alveolitis, Extrinsic Allergic [MESH:D000542] (495) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Influenza, Human [MESH:D007251] (1075) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Tuberculosis, Pulmonary [MESH:D014397] (678) |
|
|
Legionnaires' Disease [MESH:D007877] (611) |
|
|
Pneumonia, Aspiration [MESH:D011015] (824) |
|
|
|
|
|
Adenocarcinoma of lung [MESH:C538231] (1487) |
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Small Cell Lung Carcinoma [MESH:D055752] (1380) |
|
|
C09. Otorhinolaryngologic Diseases |
|
|
|
C09. Otorhinolaryngologic Diseases |
|
|
|
|
|
|
|
|
Hearing Loss [MESH:D034381] (2068) |
|
|
Vestibular Diseases [MESH:D015837] (819) |
|
|
|
|
|
|
|
|
Nasopharyngeal carcinoma [MESH:C538339] (1198) |
|
|
|
|
|
|
|
|
Nasopharyngeal carcinoma [MESH:C538339] (1198) |
|
|
|
|
|
Nasopharyngeal carcinoma [MESH:C538339] (1198) |
|
|
C10. Nervous System Diseases |
|
|
|
C10. Nervous System Diseases |
|
|
Not Fully Specified [NFS] (4027) |
|
|
Restless Legs Syndrome [MESH:D012148] (379) |
|
|
Myasthenia Gravis [MESH:D009157] (632) |
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
|
|
|
Brain Edema [MESH:D001929] (1165) |
|
|
Brain Injuries [MESH:D001930] (3429) |
|
|
|
|
|
Lewy Body Disease [MESH:D020961] (1143) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
|
|
|
Cerebral Palsy, Spastic Quadriplegic, 1 [MESH:C567853] (99) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67) |
|
|
|
|
|
|
|
|
Papilloma, Choroid Plexus [MESH:D020288] (769) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Vasospasm, Intracranial [MESH:D020301] (324) |
|
|
Ischemic Attack, Transient [MESH:D002546] (1313) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
Intracranial Aneurysm [MESH:D002532] (158) |
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1082) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
Lewy Body Disease [MESH:D020961] (1143) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Status Epilepticus [MESH:D013226] (4014) |
|
|
|
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Epilepsy, Tonic-Clonic [MESH:D004830] (1042) |
|
|
Spasms, Infantile [MESH:D013036] (468) |
|
|
|
|
|
Migraine Disorders [MESH:D008881] (2318) |
|
|
|
|
|
|
|
|
Hyperprolactinemia [MESH:D006966] (603) |
|
|
Pituitary ACTH Hypersecretion [MESH:D047748] (599) |
|
|
|
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
|
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
Scrapie [MESH:D012608] (462) |
|
|
|
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
Lewy Body Disease [MESH:D020961] (1143) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
|
|
Spinal Cord Compression [MESH:D013117] (1800) |
|
|
Spinal Cord Injuries [MESH:D013119] (1674) |
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62) |
|
|
|
|
|
Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Papilloma, Choroid Plexus [MESH:D020288] (769) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Lewy Body Disease [MESH:D020961] (1143) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62) |
|
|
Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
|
|
Scrapie [MESH:D012608] (462) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Gait Disorders, Neurologic [MESH:D020233] (491) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
Seizures [MESH:D012640] (4514) |
|
|
Catalepsy [MESH:D002375] (1429) |
|
|
Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
|
|
Lethargy [MESH:D053609] (1035) |
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
Amnesia [MESH:D000647] (1911) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67) |
|
|
Muscle Weakness [MESH:D018908] (478) |
|
|
Headache [MESH:D006261] (1416) |
|
|
Pain, Intractable [MESH:D010148] (707) |
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
Facial Paralysis [MESH:D005158] (238) |
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
|
|
|
Hearing Loss [MESH:D034381] (2068) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62) |
|
|
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62) |
|
|
|
|
|
|
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
|
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Myasthenia Gravis [MESH:D009157] (632) |
|
|
Diabetic Neuropathies [MESH:D003929] (2442) |
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
|
|
|
Sleep Deprivation [MESH:D012892] (233) |
|
|
Restless Legs Syndrome [MESH:D012148] (379) |
|
|
Restless Legs Syndrome [MESH:D012148] (379) |
|
|
Spinal Cord Injuries [MESH:D013119] (1676) |
|
|
Brain Injuries [MESH:D001930] (3431) |
|
|
C11. Eye Diseases |
|
|
|
C11. Eye Diseases |
|
|
Not Fully Specified [NFS] (245) |
|
|
Eyelid Diseases [MESH:D005141] (882) |
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Eye Pain [MESH:D058447] (207) |
|
|
|
|
|
Glaucoma, Open-Angle [MESH:D005902] (1281) |
|
|
Opsoclonus-Myoclonus Syndrome [MESH:D053578] (202) |
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
Retinal Detachment [MESH:D012163] (1639) |
|
|
Retinopathy of Prematurity [MESH:D012178] (353) |
|
|
|
|
|
Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34) |
|
|
Juvenile macular degeneration and hypotrichosis [MESH:C537698] (34) |
|
|
|
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
C12. Male Urogenital Diseases |
|
|
|
C12. Male Urogenital Diseases |
|
|
|
|
|
|
|
|
Penile Neoplasms [MESH:D010412] (890) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
|
|
|
Azoospermia [MESH:D053713] (1052) |
|
|
Penile Neoplasms [MESH:D010412] (890) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Erectile Dysfunction [MESH:D007172] (1791) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
Allanson Pantzar McLeod syndrome [MESH:C537048] (503) |
|
|
|
|
|
Penile Neoplasms [MESH:D010412] (890) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Urinary Tract Infections [MESH:D014552] (984) |
|
|
Anuria [MESH:D001002] (833) |
|
|
Diabetes Insipidus [MESH:D003919] (354) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Fanconi Syndrome [MESH:D005198] (253) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Nephrocalcinosis [MESH:D009397] (311) |
|
|
Hypertension, Renovascular [MESH:D006978] (365) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Glomerulopathy with fibronectin deposits [MESH:C536826] (244) |
|
|
Balkan Nephropathy [MESH:D001449] (772) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Nephrosis, Lipoid [MESH:D009402] (74) |
|
|
Nephrosis, congenital [MESH:C535761] (52) |
|
|
Nephrotic syndrome, idiopathic, steroid-resistant [MESH:C536404] (30) |
|
|
|
|
|
Kidney Tubular Necrosis, Acute [MESH:D007683] (974) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Fanconi Syndrome [MESH:D005198] (253) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Ureteral Obstruction [MESH:D014517] (575) |
|
|
|
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Urinary Bladder, Overactive [MESH:D053201] (530) |
|
|
Cystitis, Interstitial [MESH:D018856] (264) |
|
|
Anuria [MESH:D001002] (833) |
|
|
Hematuria [MESH:D006417] (477) |
|
|
Oliguria [MESH:D009846] (307) |
|
|
Urinary Retention [MESH:D016055] (411) |
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
|
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
C13. Female Urogenital Diseases and Pregnancy Complications |
|
|
|
C13. Female Urogenital Diseases and Pregnancy Complications |
|
|
|
|
|
Endometriosis [MESH:D004715] (2461) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
Infertility, Female [MESH:D007247] (2184) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
Endometrial Neoplasms [MESH:D016889] (1984) |
|
|
Vulvar Lichen Sclerosus [MESH:D007724] (825) |
|
|
Allanson Pantzar McLeod syndrome [MESH:C537048] (503) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Endometrial Neoplasms [MESH:D016889] (1989) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Urinary Tract Infections [MESH:D014552] (984) |
|
|
Anuria [MESH:D001002] (833) |
|
|
Diabetes Insipidus [MESH:D003919] (354) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Fanconi Syndrome [MESH:D005198] (253) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Nephrocalcinosis [MESH:D009397] (311) |
|
|
Hypertension, Renovascular [MESH:D006978] (365) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Glomerulopathy with fibronectin deposits [MESH:C536826] (244) |
|
|
Balkan Nephropathy [MESH:D001449] (772) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Nephrosis, Lipoid [MESH:D009402] (74) |
|
|
Nephrosis, congenital [MESH:C535761] (52) |
|
|
Nephrotic syndrome, idiopathic, steroid-resistant [MESH:C536404] (30) |
|
|
|
|
|
Kidney Tubular Necrosis, Acute [MESH:D007683] (974) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Fanconi Syndrome [MESH:D005198] (253) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Ureteral Obstruction [MESH:D014517] (575) |
|
|
|
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Urinary Bladder, Overactive [MESH:D053201] (530) |
|
|
Cystitis, Interstitial [MESH:D018856] (264) |
|
|
Anuria [MESH:D001002] (833) |
|
|
Hematuria [MESH:D006417] (477) |
|
|
Oliguria [MESH:D009846] (307) |
|
|
Urinary Retention [MESH:D016055] (411) |
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
|
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Diabetes, Gestational [MESH:D016640] (1157) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Fetal Growth Retardation [MESH:D005317] (986) |
|
|
Pre-Eclampsia [MESH:D011225] (1435) |
|
|
Abruptio Placentae [MESH:D000037] (430) |
|
|
Obstetric Labor, Premature [MESH:D007752] (1316) |
|
|
Abruptio Placentae [MESH:D000037] (430) |
|
|
C14. Cardiovascular Diseases |
|
|
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Heart Defects, Congenital [MESH:D006330] (2447) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Heart Arrest [MESH:D006323] (1926) |
|
|
Heart Defects, Congenital [MESH:D006330] (2443) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Pericardial Effusion [MESH:D010490] (1015) |
|
|
Atrial Fibrillation [MESH:D001281] (1053) |
|
|
Bradycardia [MESH:D001919] (1899) |
|
|
Long QT Syndrome [MESH:D008133] (693) |
|
|
Sick Sinus Syndrome [MESH:D012804] (293) |
|
|
Ventricular Premature Complexes [MESH:D018879] (418) |
|
|
Sick Sinus Syndrome [MESH:D012804] (293) |
|
|
Tachycardia, Ventricular [MESH:D017180] (1386) |
|
|
Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
|
|
Cardiomyopathy, Dilated, 1i [MESH:C565752] (62) |
|
|
Cardiomyopathy, Alcoholic [MESH:D002310] (354) |
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1516) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Endomyocardial Fibrosis [MESH:D004719] (521) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocarditis [MESH:D009205] (1708) |
|
|
Cardiomyopathy, Dilated, 1i [MESH:C565752] (62) |
|
|
Aortic Valve Insufficiency [MESH:D001022] (1002) |
|
|
|
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1451) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Unstable [MESH:D000789] (782) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Vasospasm [MESH:D003329] (533) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Ventricular Dysfunction, Left [MESH:D018487] (1631) |
|
|
|
|
|
Aortic Stenosis, Subvalvular [MESH:D001020] (203) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Hypotension [MESH:D007022] (4045) |
|
|
Vascular System Injuries [MESH:D057772] (2086) |
|
|
Aneurysm, Dissecting [MESH:D000784] (699) |
|
|
Intracranial Aneurysm [MESH:D002532] (158) |
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
|
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
Mesenteric Vascular Occlusion [MESH:D008641] (147) |
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
Vasospasm, Intracranial [MESH:D020301] (324) |
|
|
Ischemic Attack, Transient [MESH:D002546] (1313) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
Intracranial Aneurysm [MESH:D002532] (158) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1082) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
Thromboembolism [MESH:D013923] (732) |
|
|
Pulmonary Embolism [MESH:D011655] (1118) |
|
|
Thromboembolism [MESH:D013923] (732) |
|
|
Budd-Chiari Syndrome [MESH:D006502] (164) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Ehlers-Danlos syndrome type 3 [MESH:C536196] (142) |
|
|
Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
Hypertension, Essential [MESH:C562386] (1308) |
|
|
Hypertension, Malignant [MESH:D006974] (621) |
|
|
Hypertension, Pregnancy-Induced [MESH:D046110] (397) |
|
|
Hypertension, Renovascular [MESH:D006978] (365) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Unstable [MESH:D000789] (782) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Vasospasm [MESH:D003329] (533) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
C15. Hemic and Lymphatic Diseases |
|
|
|
C15. Hemic and Lymphatic Diseases |
|
|
Polycythemia [MESH:D011086] (412) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
Anemia, Sideroblastic [MESH:D000756] (636) |
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Bone Marrow failure syndromes [MESH:C536572] (248) |
|
|
Anemia, Iron-Deficiency [MESH:D018798] (547) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Platelet Glycoprotein IV Deficiency [MESH:C564245] (173) |
|
|
|
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
|
|
|
Hypoalbuminemia [MESH:D034141] (1332) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
Anemia, Sideroblastic [MESH:D000756] (636) |
|
|
Bone Marrow failure syndromes [MESH:C536572] (248) |
|
|
Polycythemia Vera [MESH:D011087] (244) |
|
|
Primary Myelofibrosis [MESH:D055728] (165) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Plasminogen Activator Inhibitor-1 Deficiency [MESH:C567640] (328) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Ehlers-Danlos syndrome type 3 [MESH:C536196] (142) |
|
|
Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
Leukocytosis [MESH:D007964] (988) |
|
|
Leukostasis [MESH:D018921] (769) |
|
|
Lymphopenia [MESH:D008231] (990) |
|
|
Neutropenia [MESH:D009503] (1629) |
|
|
Job Syndrome [MESH:D007589] (772) |
|
|
Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111) |
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II [MESH:C565531] (85) |
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142) |
|
|
|
|
|
Giant Lymph Node Hyperplasia [MESH:D005871] (1013) |
|
|
Sarcoidosis [MESH:D012507] (895) |
|
|
Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754) |
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
|
Lymphoma, Follicular [MESH:D008224] (1025) |
|
|
Lymphoma, AIDS-Related [MESH:D016483] (278) |
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
|
Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) |
|
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
Abnormalities, Drug-Induced [MESH:D000014] (1024) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
|
|
Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
|
|
|
Long QT Syndrome [MESH:D008133] (693) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
|
|
|
|
|
Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
|
|
|
Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Ehlers-Danlos syndrome type 3 [MESH:C536196] (142) |
|
|
Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Allanson Pantzar McLeod syndrome [MESH:C537048] (503) |
|
|
Fetal Growth Retardation [MESH:D005317] (986) |
|
|
Platelet Glycoprotein IV Deficiency [MESH:C564245] (173) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111) |
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II [MESH:C565531] (85) |
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67) |
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Xanthinuria, Type I [MESH:C562584] (190) |
|
|
Myeloperoxidase Deficiency [MESH:C562864] (335) |
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67) |
|
|
Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135) |
|
|
|
|
|
Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67) |
|
|
|
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Acatalasia [MESH:D020642] (788) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Arthritis, Gouty [MESH:D015210] (211) |
|
|
Fanconi Syndrome [MESH:D005198] (253) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Li-Fraumeni Syndrome [MESH:D016864] (859) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Osteogenesis imperfecta, type 2A [MESH:C536042] (375) |
|
|
Osteogenesis imperfecta, type 3 [MESH:C536044] (375) |
|
|
Osteogenesis imperfecta, type 4 [MESH:C536045] (375) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Ehlers-Danlos syndrome type 3 [MESH:C536196] (142) |
|
|
Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
Asphyxia Neonatorum [MESH:D001238] (1648) |
|
|
Bronchopulmonary Dysplasia [MESH:D001997] (1021) |
|
|
Retinopathy of Prematurity [MESH:D012178] (353) |
|
|
C17. Skin and Connective Tissue Diseases |
|
|
|
C17. Skin and Connective Tissue Diseases |
|
|
Cartilage Diseases [MESH:D002357] (438) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Keloid [MESH:D007627] (1111) |
|
|
Ehlers-Danlos syndrome type 3 [MESH:C536196] (142) |
|
|
Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
Osteogenesis imperfecta, type 2A [MESH:C536042] (375) |
|
|
Osteogenesis imperfecta, type 3 [MESH:C536044] (375) |
|
|
Osteogenesis imperfecta, type 4 [MESH:C536045] (375) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Keratosis [MESH:D007642] (1941) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Skin Neoplasms [MESH:D012878] (2991) |
|
|
|
|
|
Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
Hirsutism [MESH:D006628] (323) |
|
|
Juvenile macular degeneration and hypotrichosis [MESH:C537698] (34) |
|
|
Alopecia [MESH:D000505] (1453) |
|
|
|
|
|
Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Ehlers-Danlos syndrome type 3 [MESH:C536196] (142) |
|
|
Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Ehlers-Danlos syndrome type 3 [MESH:C536196] (142) |
|
|
Ehlers-Danlos syndrome, cardiac valvular form [MESH:C536200] (152) |
|
|
Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
|
|
|
|
|
Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
|
|
|
|
|
|
|
|
Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
|
|
Lichenoid Eruptions [MESH:D017512] (1324) |
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Urticaria [MESH:D014581] (2668) |
|
|
Pemphigoid, Bullous [MESH:D010391] (707) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
C18. Nutritional and Metabolic Diseases |
|
|
|
C18. Nutritional and Metabolic Diseases |
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
Alkalosis [MESH:D000471] (384) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Hypocalcemia [MESH:D006996] (378) |
|
|
Nephrocalcinosis [MESH:D009397] (311) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Li-Fraumeni Syndrome [MESH:D016864] (859) |
|
|
Hypoglycemia [MESH:D007003] (2420) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Diabetes, Gestational [MESH:D016640] (1152) |
|
|
Glucose Intolerance [MESH:D018149] (605) |
|
|
|
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
Anemia, Iron-Deficiency [MESH:D018798] (547) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
|
|
|
|
|
|
Hypercholesterolemia [MESH:D006937] (1404) |
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
Xanthinuria, Type I [MESH:C562584] (190) |
|
|
Myeloperoxidase Deficiency [MESH:C562864] (335) |
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67) |
|
|
Phosphoenolpyruvate carboxykinase deficiency [MESH:C536654] (135) |
|
|
|
|
|
Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67) |
|
|
|
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Acatalasia [MESH:D020642] (788) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Arthritis, Gouty [MESH:D015210] (211) |
|
|
Fanconi Syndrome [MESH:D005198] (253) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Phosphoenolpyruvate carboxykinase 2 deficiency [MESH:C536655] (67) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Hypernatremia [MESH:D006955] (215) |
|
|
Hypocalcemia [MESH:D006996] (368) |
|
|
Hypokalemia [MESH:D007008] (1041) |
|
|
Hyponatremia [MESH:D007010] (789) |
|
|
|
|
|
|
|
|
Protein Deficiency [MESH:D011488] (1057) |
|
|
Vitamin A Deficiency [MESH:D014802] (705) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
|
|
|
Proopiomelanocortin Deficiency [MESH:C565726] (200) |
|
|
Obesity, Morbid [MESH:D009767] (515) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
C19. Endocrine System Diseases |
|
|
|
C19. Endocrine System Diseases |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769) |
|
|
|
|
|
|
|
|
Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769) |
|
|
Proopiomelanocortin Deficiency [MESH:C565726] (200) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Cushing Syndrome [MESH:D003480] (282) |
|
|
Diabetes, Gestational [MESH:D016640] (1152) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Diabetic Neuropathies [MESH:D003929] (2443) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
Ovarian Neoplasms [MESH:D010051] (3275) |
|
|
Pancreatic Neoplasms [MESH:D010190] (3820) |
|
|
|
|
|
|
|
|
Adrenocortical Carcinoma, Hereditary [MESH:C565972] (769) |
|
|
Thyroid cancer, anaplastic [MESH:C536910] (489) |
|
|
Hypogonadism [MESH:D007006] (1123) |
|
|
Puberty, Delayed [MESH:D011628] (449) |
|
|
Puberty, Precocious [MESH:D011629] (1147) |
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
|
|
|
Hyperparathyroidism, Secondary [MESH:D006962] (1138) |
|
|
Diabetes Insipidus [MESH:D003919] (302) |
|
|
Hyperprolactinemia [MESH:D006966] (603) |
|
|
Pituitary ACTH Hypersecretion [MESH:D047748] (599) |
|
|
Hyperthyroidism [MESH:D006980] (1191) |
|
|
Thyroid cancer, anaplastic [MESH:C536910] (489) |
|
|
C20. Immune System Diseases |
|
|
|
C20. Immune System Diseases |
|
|
Not Fully Specified [NFS] (350) |
|
|
Graft vs Host Disease [MESH:D006086] (674) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1893) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
|
|
Pemphigoid, Bullous [MESH:D010391] (707) |
|
|
Myasthenia Gravis [MESH:D009157] (632) |
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Glomerulopathy with fibronectin deposits [MESH:C536826] (244) |
|
|
|
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Urticaria [MESH:D014581] (2668) |
|
|
Alveolitis, Extrinsic Allergic [MESH:D000542] (495) |
|
|
Asthma [MESH:D001249] (3914) |
|
|
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533) |
|
|
Lymphopenia [MESH:D008231] (990) |
|
|
Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
|
|
Job Syndrome [MESH:D007589] (772) |
|
|
Granulomatous Disease, Chronic, X-Linked [MESH:C564417] (111) |
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type II [MESH:C565531] (85) |
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142) |
|
|
|
|
|
Giant Lymph Node Hyperplasia [MESH:D005871] (1013) |
|
|
Multiple Myeloma [MESH:D009101] (2767) |
|
|
Precursor Cell Lymphoblastic Leukemia-Lymphoma [MESH:D054198] (1754) |
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
|
Lymphoma, Follicular [MESH:D008224] (1025) |
|
|
Lymphoma, AIDS-Related [MESH:D016483] (278) |
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
|
Lymphoma, T-Cell, Cutaneous [MESH:D016410] (912) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
C22. Animal Diseases |
|
|
|
C22. Animal Diseases |
|
|
Disease Models, Animal [MESH:D004195] (2058) |
|
|
Mammary Neoplasms, Animal [MESH:D015674] (2735) |
|
|
Salmonella Infections, Animal [MESH:D012481] (604) |
|
|
Scrapie [MESH:D012608] (462) |
|
|
C23. Pathological Conditions, Signs and Symptoms |
|
|
|
C23. Pathological Conditions, Signs and Symptoms |
|
|
Alopecia [MESH:D000505] (1383) |
|
|
Atrophy [MESH:D001284] (2603) |
|
|
Plaque, Atherosclerotic [MESH:D058226] (696) |
|
|
|
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Hernia, Diaphragmatic [MESH:D006548] (2647) |
|
|
Hepatomegaly [MESH:D006529] (1169) |
|
|
Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
|
|
Leukoplakia, Oral [MESH:D007972] (921) |
|
|
Intestinal Polyps [MESH:D007417] (1592) |
|
|
Emphysema [MESH:D004646] (1096) |
|
|
Gliosis [MESH:D005911] (1419) |
|
|
Hyperbilirubinemia [MESH:D006932] (1860) |
|
|
Hyperplasia [MESH:D006965] (2463) |
|
|
Ischemia [MESH:D007511] (3049) |
|
|
Leukocytosis [MESH:D007964] (978) |
|
|
Metaplasia [MESH:D008679] (1469) |
|
|
Muscle Weakness [MESH:D018908] (478) |
|
|
Neointima [MESH:D058426] (814) |
|
|
Nerve Degeneration [MESH:D009410] (4061) |
|
|
Atrial Fibrillation [MESH:D001281] (1053) |
|
|
Bradycardia [MESH:D001919] (1899) |
|
|
Long QT Syndrome [MESH:D008133] (691) |
|
|
Sick Sinus Syndrome [MESH:D012804] (293) |
|
|
Ventricular Premature Complexes [MESH:D018879] (418) |
|
|
Sick Sinus Syndrome [MESH:D012804] (293) |
|
|
Tachycardia, Ventricular [MESH:D017180] (1386) |
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Chromosome 17 deletion [MESH:C538045] (769) |
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Death, Sudden [MESH:D003645] (725) |
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Disease Progression [MESH:D018450] (2868) |
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Recurrence [MESH:D012008] (830) |
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Keloid [MESH:D007627] (1110) |
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Granuloma, Respiratory Tract [MESH:D015769] (502) |
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Fetal Growth Retardation [MESH:D005317] (986) |
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Hematuria [MESH:D006417] (477) |
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Shock, Hemorrhagic [MESH:D012771] (2042) |
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Peptic Ulcer Hemorrhage [MESH:D010438] (553) |
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Cerebral Hemorrhage [MESH:D002543] (2872) |
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Subarachnoid Hemorrhage [MESH:D013345] (1081) |
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Neurogenic Inflammation [MESH:D020078] (2246) |
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Shock, Septic [MESH:D012772] (1830) |
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Endotoxemia [MESH:D019446] (1289) |
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Femur Head Necrosis [MESH:D005271] (266) |
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Anaplasia [MESH:D000708] (348) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Recurrence, Local [MESH:D009364] (1949) |
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Neoplasm, Residual [MESH:D018365] (478) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Lymphatic Metastasis [MESH:D008207] (917) |
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Myocardial Reperfusion Injury [MESH:D015428] (3500) |
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Multiple Organ Failure [MESH:D009102] (1836) |
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Shock, Hemorrhagic [MESH:D012771] (2042) |
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Shock, Septic [MESH:D012772] (1830) |
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Chills [MESH:D023341] (644) |
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Edema [MESH:D004487] (3726) |
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Flushing [MESH:D005483] (506) |
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Reticulocytosis [MESH:D045262] (514) |
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Fever [MESH:D005334] (2856) |
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Hypothermia [MESH:D007035] (2075) |
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Weight Gain [MESH:D015430] (2595) |
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Cachexia [MESH:D002100] (2283) |
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Proopiomelanocortin Deficiency [MESH:C565726] (200) |
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Obesity, Morbid [MESH:D009767] (515) |
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Eye Pain [MESH:D058447] (207) |
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Gait Disorders, Neurologic [MESH:D020233] (491) |
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Seizures [MESH:D012640] (4502) |
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Catalepsy [MESH:D002375] (1429) |
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Lethargy [MESH:D053609] (1035) |
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Learning Disorders [MESH:D007859] (2727) |
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Amnesia [MESH:D000647] (1911) |
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Muscle Weakness [MESH:D018908] (478) |
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Headache [MESH:D006261] (1417) |
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Pain, Intractable [MESH:D010148] (707) |
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Neuralgia, Postherpetic [MESH:D051474] (742) |
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Facial Paralysis [MESH:D005158] (238) |
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Gastroparesis [MESH:D018589] (732) |
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Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
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Hearing Loss [MESH:D034381] (2066) |
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Hyperalgesia [MESH:D006930] (3929) |
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Sleep Deprivation [MESH:D012892] (233) |
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Eye Pain [MESH:D058447] (207) |
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Headache [MESH:D006261] (1417) |
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Pain, Intractable [MESH:D010148] (707) |
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Acute Coronary Syndrome [MESH:D054058] (2286) |
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Angina, Unstable [MESH:D000789] (782) |
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Angina, Stable [MESH:D060050] (1702) |
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Neuralgia, Postherpetic [MESH:D051474] (742) |
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Constipation [MESH:D003248] (506) |
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Hyperphagia [MESH:D006963] (206) |
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Nausea [MESH:D009325] (2300) |
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Vomiting [MESH:D014839] (1354) |
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Anoxia [MESH:D000860] (1698) |
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Hypercalciuria [MESH:D053565] (330) |
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Oliguria [MESH:D009846] (307) |
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Urinary Bladder, Overactive [MESH:D053201] (530) |
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Albuminuria [MESH:D000419] (2394) |
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Hirsutism [MESH:D006628] (323) |
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C24. Occupational Diseases |
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C24. Occupational Diseases |
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Not Fully Specified [NFS] (1530) |
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Asbestosis [MESH:D001195] (935) |
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Berylliosis [MESH:D001607] (2005) |
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Silicosis [MESH:D012829] (1273) |
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C25. Chemically-Induced Disorders |
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C25. Chemically-Induced Disorders |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
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Asthma, Aspirin-Induced [MESH:D055963] (1055) |
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Stevens-Johnson Syndrome [MESH:D013262] (1163) |
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Arsenic Poisoning [MESH:D020261] (2540) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Manganese Poisoning [MESH:D020149] (2214) |
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Psychoses, Substance-Induced [MESH:D011605] (2053) |
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Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
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Amphetamine-Related Disorders [MESH:D019969] (2858) |
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Cocaine-Related Disorders [MESH:D019970] (3054) |
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Drug Overdose [MESH:D062787] (513) |
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Psychoses, Substance-Induced [MESH:D011605] (2052) |
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Substance Withdrawal Syndrome [MESH:D013375] (2956) |
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Cardiomyopathy, Alcoholic [MESH:D002310] (354) |
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Fatty Liver, Alcoholic [MESH:D005235] (657) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Heroin Dependence [MESH:D006556] (950) |
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C26. Wounds and Injuries |
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C26. Wounds and Injuries |
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Not Fully Specified [NFS] (2454) |
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Burns [MESH:D002056] (2565) |
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Vascular System Injuries [MESH:D057772] (2086) |
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Brain Injuries [MESH:D001930] (3431) |
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Radiation Injuries, Experimental [MESH:D011833] (2662) |
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Spinal Cord Compression [MESH:D013117] (1800) |
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Lung Injury [MESH:D055370] (1814) |
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Brain Injuries [MESH:D001930] (3431) |
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D02. Organic Chemicals |
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D02. Organic Chemicals |
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Acetophenones [MESH:D000098] (180) |
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D27. Chemical Actions and Uses |
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D27. Chemical Actions and Uses |
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Antioxidants [MESH:D000975] (72) |
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Enzyme Inhibitors [MESH:D004791] (520) |
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Anti-Inflammatory Agents, Non-Steroidal [MESH:D000894] (115) |
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Antioxidants [MESH:D000975] (62) |
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Anti-Inflammatory Agents, Non-Steroidal [MESH:D000894] (115) |
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Anti-Inflammatory Agents, Non-Steroidal [MESH:D000894] (115) |
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Antioxidants [MESH:D000975] (62) |
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
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Proopiomelanocortin Deficiency [MESH:C565726] (200) |
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G. Phenomena and Processes |
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G. Phenomena and Processes |
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Chromosome 17 deletion [MESH:C538045] (769) |
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Chromosome 17 deletion [MESH:C538045] (769) |
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Chromosome 17 deletion [MESH:C538045] (769) |
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Chromosome 17 deletion [MESH:C538045] (769) |
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Chromosome 17 deletion [MESH:C538045] (769) |
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Chromosome 17 deletion [MESH:C538045] (769) |
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Proopiomelanocortin Deficiency [MESH:C565726] (200) |
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