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 1 [HGNC:NFKB1] (254) |
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hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor) [HGNC:HIF1A] (212) |
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S100 calcium binding protein B [HGNC:S100B] (17) |
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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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tumor necrosis factor receptor superfamily, member 10b [HGNC:TNFRSF10B] (124) |
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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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integrin, alpha M (complement component 3 receptor 3 subunit) [HGNC:ITGAM] (75) |
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S100 calcium binding protein B [HGNC:S100B] (17) |
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adiponectin, C1Q and collagen domain containing [HGNC:ADIPOQ] (71) |
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chemokine (C-C motif) ligand 02 [HGNC:CCL2] (337) |
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interleukin 08 [HGNC:IL8] (649) |
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fibronectin 1 [HGNC:FN1] (112) |
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forkhead box O1 [HGNC:FOXO1] (45) |
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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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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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interleukin 18 (interferon-gamma-inducing factor) [HGNC:IL18] (73) |
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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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mitogen-activated protein kinase 14 [HGNC:MAPK14] (162) |
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signal transducer and activator of transcription 3 (acute-phase response factor) [HGNC:STAT3] (145) |
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transient receptor potential cation channel, subfamily C, member 6 [HGNC:TRPC6] (14) |
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tumor necrosis factor [HGNC:TNF] (795) |
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tumor necrosis factor receptor superfamily, member 10b [HGNC:TNFRSF10B] (124) |
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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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activity (2549) |
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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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localization (244) |
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metabolic processing (740) |
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oxidation (295) |
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phosphorylation (1060) |
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reaction (1574) |
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secretion (901) |
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A. Anatomy |
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A. Anatomy |
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Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
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Allanson Pantzar McLeod syndrome [MESH:C537048] (503) |
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Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238) |
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Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
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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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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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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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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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Endotoxemia [MESH:D019446] (1289) |
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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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Papillomavirus Infections [MESH:D030361] (630) |
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Hepatitis B [MESH:D006509] (976) |
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Sarcoma, Kaposi [MESH:D012514] (1578) |
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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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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 Seropositivity [MESH:D006679] (480) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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HIV Seropositivity [MESH:D006679] (480) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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Papillomavirus Infections [MESH:D030361] (537) |
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C03. Parasitic Diseases |
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C03. Parasitic Diseases |
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Trichuriasis [MESH:D014257] (805) |
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Schistosomiasis mansoni [MESH:D012555] (1033) |
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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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Follicular Cyst [MESH:D005497] (151) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Leukemia, T-Cell [MESH:D015458] (395) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354) |
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032) |
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Leukemia, Myelomonocytic, Juvenile [MESH:D054429] (344) |
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Leukemia, Promyelocytic, Acute [MESH:D015473] (1367) |
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Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420) |
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Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
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Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420) |
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Carcinosarcoma [MESH:D002296] (581) |
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Metachondromatosis [MESH:C562938] (49) |
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Mastocytosis, Systemic [MESH:D034721] (769) |
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Osteosarcoma [MESH:D012516] (2175) |
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Metachondromatosis [MESH:C562938] (49) |
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Fibromatosis, Aggressive [MESH:D018222] (1562) |
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Leiomyosarcoma [MESH:D007890] (977) |
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Rhabdomyosarcoma, Alveolar [MESH:D018232] (149) |
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Carcinosarcoma [MESH:D002296] (581) |
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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, Kaposi [MESH:D012514] (1578) |
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Rhabdomyosarcoma, Alveolar [MESH:D018232] (149) |
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Gliosarcoma [MESH:D018316] (880) |
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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 [MESH:D008545] (3508) |
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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, Lewis Lung [MESH:D018827] (248) |
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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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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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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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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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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Mesothelioma [MESH:D008654] (2567) |
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Gliosarcoma [MESH:D018316] (880) |
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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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Gliosarcoma [MESH:D018316] (880) |
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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 [MESH:D008545] (3508) |
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Multiple Myeloma [MESH:D009101] (2767) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Sarcoma, Kaposi [MESH:D012514] (1578) |
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Hemangioblastoma [MESH:D018325] (395) |
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Melanoma [MESH:D008545] (3508) |
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Skin Neoplasms [MESH:D012878] (2992) |
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Soft Tissue Neoplasms [MESH:D012983] (2003) |
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Metachondromatosis [MESH:C562938] (49) |
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Nose Neoplasms [MESH:D009669] (384) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Bile Duct Neoplasms [MESH:D001650] (367) |
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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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Rectal Neoplasms [MESH:D012004] (717) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Pituitary Neoplasms [MESH:D010911] (981) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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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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Nose Neoplasms [MESH:D009669] (390) |
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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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Pituitary Neoplasms [MESH:D010911] (914) |
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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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Uterine Cervical Neoplasms [MESH:D002583] (978) |
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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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Carcinoma, Lewis Lung [MESH:D018827] (248) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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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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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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Tuberous Sclerosis [MESH:D014402] (635) |
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Metachondromatosis [MESH:C562938] (49) |
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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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Osteonecrosis [MESH:D010020] (539) |
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Acromicric dysplasia [MESH:C535662] (520) |
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Marfan Syndrome [MESH:D008382] (646) |
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Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
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Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
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Antley-Bixler Syndrome Phenotype [MESH:D054882] (284) |
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Spondyloepimetaphyseal Dysplasia, Missouri Type [MESH:C566574] (142) |
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Metaphyseal Anadysplasia 2 [MESH:C567771] (452) |
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Camurati-Engelmann Syndrome [MESH:D003966] (492) |
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Enchondromatosis [MESH:D004687] (170) |
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Metachondromatosis [MESH:C562938] (49) |
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Acromegaly [MESH:D000172] (466) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Metachondromatosis [MESH:C562938] (49) |
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Nose Neoplasms [MESH:D009669] (384) |
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Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
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Metachondromatosis [MESH:C562938] (49) |
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Intervertebral disc disease [MESH:C535531] (514) |
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Intervertebral disc disease [MESH:C535531] (514) |
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Kyphosis [MESH:D007738] (637) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Mandibular Diseases [MESH:D008336] (395) |
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Maxillary Diseases [MESH:D008439] (354) |
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Cleft Palate [MESH:D002972] (1330) |
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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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Osteoarthritis [MESH:D010003] (1743) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Rhabdomyolysis [MESH:D012206] (465) |
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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) |
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Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
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Dermatomyositis [MESH:D003882] (1826) |
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Dermatomyositis [MESH:D003882] (1826) |
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Costello Syndrome [MESH:D056685] (407) |
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LEOPARD Syndrome [MESH:D044542] (299) |
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Noonan Syndrome [MESH:D009634] (506) |
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Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
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Cleft Palate [MESH:D002972] (1330) |
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Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Acromicric dysplasia [MESH:C535662] (520) |
|
|
Metaphyseal Anadysplasia 2 [MESH:C567771] (452) |
|
|
Antley-Bixler Syndrome Phenotype [MESH:D054882] (284) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Osteoarthritis [MESH:D010003] (1743) |
|
 |
C06. Digestive System Diseases |
 |
 |
|
C06. Digestive System Diseases |
|
|
|
|
|
|
|
|
Bile Duct Neoplasms [MESH:D001650] (367) |
|
|
|
|
|
Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
Bile Duct Neoplasms [MESH:D001650] (367) |
|
|
Barrett Esophagus [MESH:D001471] (1930) |
|
|
|
|
|
Bile Duct Neoplasms [MESH:D001650] (367) |
|
|
Stomach Neoplasms [MESH:D013274] (4942) |
|
|
Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
|
|
Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
|
|
|
|
|
Rectal Neoplasms [MESH:D012004] (717) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Carcinoma, Hepatocellular [MESH:D006528] (5375) |
|
|
Liver Neoplasms, Experimental [MESH:D008114] (2837) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
|
|
|
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) |
|
|
|
|
|
Rectal Neoplasms [MESH:D012004] (717) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
|
|
|
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) |
|
|
|
|
|
Rectal Neoplasms [MESH:D012004] (717) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
|
|
|
Rectal Neoplasms [MESH:D012004] (717) |
|
|
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) |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hypertension, Portal [MESH:D006975] (869) |
|
|
Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
|
|
Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567) |
|
|
|
|
|
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) |
|
|
Hepatitis, Alcoholic [MESH:D006519] (1613) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
|
Carcinoma, Hepatocellular [MESH:D006528] (5375) |
|
|
Liver Neoplasms, Experimental [MESH:D008114] (2837) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
Pancreatitis [MESH:D010195] (1924) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
Peritoneal Fibrosis [MESH:D056627] (488) |
|
|
Peritonitis [MESH:D010538] (800) |
|
 |
C07. Stomatognathic Diseases |
 |
 |
|
C07. Stomatognathic Diseases |
|
|
|
|
|
Mandibular Diseases [MESH:D008336] (450) |
|
|
Maxillary Diseases [MESH:D008439] (354) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Periapical Periodontitis [MESH:D010485] (183) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
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) |
|
|
|
|
|
Periapical Periodontitis [MESH:D010485] (183) |
|
|
Periapical Periodontitis [MESH:D010485] (183) |
|
|
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) |
|
|
Bronchitis, Chronic [MESH:D029481] (569) |
|
|
Bronchiolitis Obliterans [MESH:D001989] (611) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
Hypertension, Pulmonary [MESH:D006976] (2000) |
|
|
Pulmonary Edema [MESH:D011654] (2109) |
|
|
Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
|
|
Tuberculosis, Pulmonary [MESH:D014397] (678) |
|
|
Alveolitis, Extrinsic Allergic [MESH:D000542] (496) |
|
|
Idiopathic Pulmonary Fibrosis [MESH:D054990] (310) |
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Asbestosis [MESH:D001195] (935) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
Silicosis [MESH:D012829] (1273) |
|
|
Asthma [MESH:D001249] (3903) |
|
|
Bronchitis, Chronic [MESH:D029481] (569) |
|
|
Bronchiolitis Obliterans [MESH:D001989] (611) |
|
|
Bronchitis, Chronic [MESH:D029481] (569) |
|
|
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) |
|
|
Idiopathic Pulmonary Fibrosis [MESH:D054990] (310) |
|
|
Nose Neoplasms [MESH:D009669] (390) |
|
|
Rhinitis, Allergic, Perennial [MESH:D012221] (625) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
|
|
Alveolitis, Extrinsic Allergic [MESH:D000542] (495) |
|
|
Rhinitis, Allergic, Perennial [MESH:D012221] (625) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Influenza, Human [MESH:D007251] (1075) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Tuberculosis, Pulmonary [MESH:D014397] (678) |
|
|
Bronchitis, Chronic [MESH:D029481] (569) |
|
|
Legionnaires' Disease [MESH:D007877] (611) |
|
|
Pneumonia, Aspiration [MESH:D011015] (824) |
|
|
Nose Neoplasms [MESH:D009669] (390) |
|
|
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 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
|
|
Nose Neoplasms [MESH:D009669] (390) |
|
|
Rhinitis, Allergic, Perennial [MESH:D012221] (625) |
|
|
Nose Neoplasms [MESH:D009669] (390) |
|
|
|
|
|
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) |
|
|
Sleep Disorders [MESH:D012893] (2050) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
|
|
|
Brain Edema [MESH:D001929] (1165) |
|
|
Brain Injuries [MESH:D001930] (3429) |
|
|
|
|
|
|
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
Parkinson Disease 7, Autosomal Recessive Early-Onset [MESH:C565238] (62) |
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
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) |
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Status Epilepticus [MESH:D013226] (4014) |
|
|
|
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Epilepsy, Temporal Lobe [MESH:D004833] (1108) |
|
|
Epilepsy, Tonic-Clonic [MESH:D004830] (1042) |
|
|
|
|
|
Migraine Disorders [MESH:D008881] (2318) |
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
Pituitary Neoplasms [MESH:D010911] (981) |
|
|
Acromegaly [MESH:D000172] (466) |
|
|
|
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
|
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
|
|
|
|
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
Parkinson Disease 7, Autosomal Recessive Early-Onset [MESH:C565238] (62) |
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
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) |
|
|
|
|
|
|
|
|
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) |
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
|
|
|
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) |
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62) |
|
|
Parkinson Disease 7, Autosomal Recessive Early-Onset [MESH:C565238] (62) |
|
|
Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
Seizures [MESH:D012640] (4514) |
|
|
Catalepsy [MESH:D002375] (1429) |
|
|
Lethargy [MESH:D053609] (1035) |
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
Amnesia [MESH:D000647] (1911) |
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Cri-du-Chat Syndrome [MESH:D003410] (139) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Muscular Atrophy [MESH:D009133] (1234) |
|
|
Headache [MESH:D006261] (1416) |
|
|
Pain, Intractable [MESH:D010148] (707) |
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
|
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
|
|
|
|
|
|
|
|
|
Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
Paresthesia [MESH:D010292] (416) |
|
|
|
|
|
|
|
|
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) |
|
|
Diabetic Neuropathies [MESH:D003929] (2442) |
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
|
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
Spinal Cord Injuries [MESH:D013119] (1676) |
|
|
Brain Injuries [MESH:D001930] (3431) |
|
 |
C11. Eye Diseases |
 |
 |
|
C11. Eye Diseases |
|
|
Eyelid Diseases [MESH:D005141] (882) |
|
|
Corneal Neovascularization [MESH:D016510] (622) |
|
|
Keratoconus [MESH:D007640] (121) |
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Dry Eye Syndromes [MESH:D015352] (533) |
|
|
|
|
|
Glaucoma, Open-Angle [MESH:D005902] (1281) |
|
|
|
|
|
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) |
|
|
Retinal Vein Occlusion [MESH:D012170] (607) |
|
|
Retinopathy of Prematurity [MESH:D012178] (353) |
|
|
|
|
|
Macular Edema [MESH:D008269] (557) |
|
|
|
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
Choroidal Neovascularization [MESH:D020256] (550) |
|
|
|
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C12. Male Urogenital Diseases |
 |
 |
|
C12. Male Urogenital Diseases |
|
|
|
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Penile Induration [MESH:D010411] (495) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Erectile Dysfunction [MESH:D007172] (1791) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
Allanson Pantzar McLeod syndrome [MESH:C537048] (503) |
|
|
|
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
|
|
|
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) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Hypertension, Renal [MESH:D006977] (698) |
|
|
|
|
|
Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranous [MESH:D015433] (642) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
Glomerulopathy with fibronectin deposits [MESH:C536826] (244) |
|
|
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) |
|
|
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) |
|
|
Anuria [MESH:D001002] (833) |
|
|
Urinary Retention [MESH:D016055] (411) |
|
|
Albuminuria [MESH:D000419] (2394) |
|
 |
C13. Female Urogenital Diseases and Pregnancy Complications |
 |
 |
|
C13. Female Urogenital Diseases and Pregnancy Complications |
|
|
Not Fully Specified [NFS] (1116) |
|
|
|
|
|
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) |
|
|
|
|
|
Uterine Cervical Neoplasms [MESH:D002583] (978) |
|
|
Endometrial Neoplasms [MESH:D016889] (1984) |
|
|
Uterine Cervical Neoplasms [MESH:D002583] (978) |
|
|
Allanson Pantzar McLeod syndrome [MESH:C537048] (503) |
|
|
|
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Endometrial Neoplasms [MESH:D016889] (1989) |
|
|
Uterine Cervical Neoplasms [MESH:D002583] (978) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Urinary Tract Infections [MESH:D014552] (984) |
|
|
Anuria [MESH:D001002] (833) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Hypertension, Renal [MESH:D006977] (698) |
|
|
|
|
|
Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranous [MESH:D015433] (642) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
Glomerulopathy with fibronectin deposits [MESH:C536826] (244) |
|
|
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) |
|
|
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) |
|
|
Anuria [MESH:D001002] (833) |
|
|
Urinary Retention [MESH:D016055] (411) |
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Diabetes, Gestational [MESH:D016640] (1157) |
|
|
Placenta Diseases [MESH:D010922] (1781) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
|
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Pre-Eclampsia [MESH:D011225] (1435) |
|
|
Obstetric Labor, Premature [MESH:D007752] (1316) |
|
|
Prenatal Exposure Delayed Effects [MESH:D011297] (870) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
|
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
LEOPARD Syndrome [MESH:D044542] (299) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Noonan Syndrome [MESH:D009634] (506) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Heart Arrest [MESH:D006323] (1926) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Pericardial Effusion [MESH:D010490] (1015) |
|
|
Ventricular Outflow Obstruction [MESH:D014694] (976) |
|
|
Atrial Fibrillation [MESH:D001281] (1053) |
|
|
Bradycardia [MESH:D001919] (1899) |
|
|
Tachycardia [MESH:D013610] (3339) |
|
|
Ventricular Fibrillation [MESH:D014693] (624) |
|
|
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) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
LEOPARD Syndrome [MESH:D044542] (299) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Noonan Syndrome [MESH:D009634] (506) |
|
|
Aortic Valve Insufficiency [MESH:D001022] (1002) |
|
|
|
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1451) |
|
|
LEOPARD Syndrome [MESH:D044542] (299) |
|
|
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 Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Ventricular Dysfunction, Left [MESH:D018487] (1631) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Hypotension [MESH:D007022] (4045) |
|
|
Retinal Vein Occlusion [MESH:D012170] (607) |
|
|
Vascular System Injuries [MESH:D057772] (2086) |
|
|
Aneurysm, Dissecting [MESH:D000784] (699) |
|
|
Intracranial Aneurysm [MESH:D002532] (158) |
|
|
Aortic Rupture [MESH:D001019] (637) |
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
Aortic Aneurysm, Thoracic [MESH:D017545] (781) |
|
|
Aortic Rupture [MESH:D001019] (637) |
|
|
|
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
Aortic Aneurysm, Thoracic [MESH:D017545] (781) |
|
|
Aortic Rupture [MESH:D001019] (637) |
|
|
|
|
|
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) |
|
|
|
|
|
|
|
|
Retinal Vein Occlusion [MESH:D012170] (607) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Hypertension, Essential [MESH:C562386] (1308) |
|
|
Hypertension, Malignant [MESH:D006974] (621) |
|
|
Hypertension, Renal [MESH:D006977] (698) |
|
|
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 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 |
|
|
|
|
|
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) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
|
|
|
|
|
|
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) |
|
|
Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Leukocytosis [MESH:D007964] (988) |
|
|
Leukostasis [MESH:D018921] (769) |
|
|
Lymphopenia [MESH:D008231] (990) |
|
|
Neutropenia [MESH:D009503] (1629) |
|
|
|
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142) |
|
|
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283) |
|
|
|
|
|
Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
|
|
Giant Lymph Node Hyperplasia [MESH:D005871] (1013) |
|
|
Sarcoidosis [MESH:D012507] (895) |
|
|
Leukemia, T-Cell [MESH:D015458] (395) |
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354) |
|
|
|
|
|
Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420) |
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
 |
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
 |
 |
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
|
|
|
Costello Syndrome [MESH:D056685] (407) |
|
|
Cri-du-Chat Syndrome [MESH:D003410] (139) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
LEOPARD Syndrome [MESH:D044542] (299) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
|
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
LEOPARD Syndrome [MESH:D044542] (299) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Noonan Syndrome [MESH:D009634] (506) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238) |
|
|
Cri-du-Chat Syndrome [MESH:D003410] (139) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
|
|
|
|
|
LEOPARD Syndrome [MESH:D044542] (299) |
|
|
Noonan Syndrome [MESH:D009634] (506) |
|
|
Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Acromicric dysplasia [MESH:C535662] (520) |
|
|
Metaphyseal Anadysplasia 2 [MESH:C567771] (452) |
|
|
Antley-Bixler Syndrome Phenotype [MESH:D054882] (284) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Allanson Pantzar McLeod syndrome [MESH:C537048] (503) |
|
|
|
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
|
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
|
|
Camurati-Engelmann Syndrome [MESH:D003966] (492) |
|
|
Costello Syndrome [MESH:D056685] (407) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238) |
|
|
Cri-du-Chat Syndrome [MESH:D003410] (139) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Rubinstein-Taybi Syndrome [MESH:D012415] (149) |
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130) |
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Scapuloperoneal Syndrome, Neurogenic, Kaeser Type [MESH:C566695] (62) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
|
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
Antley-Bixler Syndrome Phenotype [MESH:D054882] (284) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Metachondromatosis [MESH:C562938] (49) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Asphyxia Neonatorum [MESH:D001238] (1648) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
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) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Noonan Syndrome [MESH:D009634] (506) |
|
|
Penile Induration [MESH:D010411] (495) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Keloid [MESH:D007627] (1111) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Skin Neoplasms [MESH:D012878] (2991) |
|
|
Chloracne [MESH:D054506] (1274) |
|
|
|
|
|
Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Serum Sickness [MESH:D012713] (484) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
Chloracne [MESH:D054506] (1274) |
|
|
|
|
|
Alopecia [MESH:D000505] (1453) |
|
|
|
|
|
|
|
|
|
|
|
LEOPARD Syndrome [MESH:D044542] (299) |
|
|
|
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Dyskeratosis Congenita, Autosomal Dominant [MESH:C565079] (130) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
|
|
|
|
|
|
|
|
|
Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
|
|
|
|
|
Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
|
|
Lichenoid Eruptions [MESH:D017512] (1324) |
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
Pemphigoid, Bullous [MESH:D010391] (707) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
 |
C18. Nutritional and Metabolic Diseases |
 |
 |
|
C18. Nutritional and Metabolic Diseases |
|
|
Not Fully Specified [NFS] (817) |
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
Alkalosis [MESH:D000471] (384) |
|
|
|
|
|
Diabetic Ketoacidosis [MESH:D016883] (226) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Calcinosis [MESH:D002114] (2989) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Hypoglycemia [MESH:D007003] (2420) |
|
|
Diabetes Mellitus, Permanent Neonatal [MESH:C563425] (321) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes, Gestational [MESH:D016640] (1152) |
|
|
Diabetic Ketoacidosis [MESH:D016883] (226) |
|
|
Diabetes Mellitus, Insulin-Dependent, 2 [MESH:C565100] (225) |
|
|
Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293) |
|
|
Glucose Intolerance [MESH:D018149] (605) |
|
|
|
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
|
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
|
|
|
|
|
|
Hypercholesterolemia [MESH:D006937] (1404) |
|
|
Hypertriglyceridemia [MESH:D015228] (808) |
|
|
Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
|
|
|
Methylmalonic acidemia [MESH:C537358] (764) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
|
|
|
|
|
|
Gaucher Disease [MESH:D005776] (299) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
Antley-Bixler Syndrome Phenotype [MESH:D054882] (284) |
|
|
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) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
|
|
|
Mandibuloacral dysplasia with type A lipodystrophy [MESH:C535705] (490) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Hyperkalemia [MESH:D006947] (485) |
|
|
Hypokalemia [MESH:D007008] (1041) |
|
|
Hyponatremia [MESH:D007010] (789) |
|
|
|
|
|
|
|
|
|
|
|
Vitamin A Deficiency [MESH:D014802] (705) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
|
|
|
Obesity, Morbid [MESH:D009767] (515) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
|
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Diabetes Mellitus, Permanent Neonatal [MESH:C563425] (321) |
|
|
Diabetes, Gestational [MESH:D016640] (1152) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Diabetic Ketoacidosis [MESH:D016883] (226) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Diabetic Neuropathies [MESH:D003929] (2443) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
Diabetes Mellitus, Insulin-Dependent, 2 [MESH:C565100] (225) |
|
|
Maturity-Onset Diabetes of the Young, Type 1 [MESH:C565101] (293) |
|
|
Ovarian Neoplasms [MESH:D010051] (3275) |
|
|
Pituitary Neoplasms [MESH:D010911] (981) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
Thyroid cancer, anaplastic [MESH:C536910] (489) |
|
|
Hypogonadism [MESH:D007006] (1123) |
|
|
Puberty, Precocious [MESH:D011629] (1147) |
|
|
|
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
|
|
|
Hyperparathyroidism, Secondary [MESH:D006962] (1138) |
|
|
Pituitary Neoplasms [MESH:D010911] (981) |
|
|
Acromegaly [MESH:D000172] (466) |
|
|
Hyperthyroidism [MESH:D006980] (1191) |
|
|
Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478) |
|
|
Thyroid cancer, anaplastic [MESH:C536910] (489) |
|
 |
C20. Immune System Diseases |
 |
 |
|
C20. Immune System Diseases |
|
|
Graft vs Host Disease [MESH:D006086] (674) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranous [MESH:D015433] (642) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
Pemphigoid, Bullous [MESH:D010391] (707) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Diabetes Mellitus, Insulin-Dependent, 2 [MESH:C565100] (225) |
|
|
Lupus Nephritis [MESH:D008181] (602) |
|
|
Glomerulopathy with fibronectin deposits [MESH:C536826] (244) |
|
|
|
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Serum Sickness [MESH:D012713] (484) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Alveolitis, Extrinsic Allergic [MESH:D000542] (495) |
|
|
Asthma [MESH:D001249] (3914) |
|
|
Rhinitis, Allergic, Perennial [MESH:D012221] (625) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
Serum Sickness [MESH:D012713] (484) |
|
|
Lymphopenia [MESH:D008231] (990) |
|
|
Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
|
|
HIV Seropositivity [MESH:D006679] (480) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
|
|
|
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I [MESH:C565532] (142) |
|
|
Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant [MESH:C567925] (283) |
|
|
|
|
|
Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
|
|
Giant Lymph Node Hyperplasia [MESH:D005871] (1013) |
|
|
Multiple Myeloma [MESH:D009101] (2767) |
|
|
Leukemia, T-Cell [MESH:D015458] (395) |
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma [MESH:D015452] (354) |
|
|
|
|
|
|
|
|
Lymphoma, Large B-Cell, Diffuse [MESH:D016403] (2012) |
|
|
Lymphoma, Large-Cell, Anaplastic [MESH:D017728] (420) |
|
|
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) |
|
 |
C23. Pathological Conditions, Signs and Symptoms |
 |
 |
|
C23. Pathological Conditions, Signs and Symptoms |
|
|
Alopecia [MESH:D000505] (1383) |
|
|
Plaque, Atherosclerotic [MESH:D058226] (696) |
|
|
Ventricular Remodeling [MESH:D020257] (686) |
|
|
Muscular Atrophy [MESH:D009133] (1234) |
|
|
Hernia, Diaphragmatic [MESH:D006548] (2647) |
|
|
Intervertebral disc disease [MESH:C535531] (514) |
|
|
|
|
|
Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
|
|
Leukoplakia, Oral [MESH:D007972] (921) |
|
|
Intestinal Polyps [MESH:D007417] (1592) |
|
|
Gliosis [MESH:D005911] (1419) |
|
|
Hyperbilirubinemia [MESH:D006932] (1860) |
|
|
Hyperplasia [MESH:D006965] (2463) |
|
|
Ischemia [MESH:D007511] (3049) |
|
|
Leukocytosis [MESH:D007964] (978) |
|
|
Neointima [MESH:D058426] (814) |
|
|
Nerve Degeneration [MESH:D009410] (4061) |
|
|
Atrial Fibrillation [MESH:D001281] (1053) |
|
|
Bradycardia [MESH:D001919] (1899) |
|
|
Tachycardia [MESH:D013610] (3339) |
|
|
Ventricular Fibrillation [MESH:D014693] (624) |
|
|
|
|
|
|
|
|
|
|
|
Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238) |
|
|
Death, Sudden [MESH:D003645] (725) |
|
|
Disease Progression [MESH:D018450] (2868) |
|
|
Disease Susceptibility [MESH:D004198] (1200) |
|
|
Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
|
|
Peritoneal Fibrosis [MESH:D056627] (488) |
|
|
Keloid [MESH:D007627] (1110) |
|
|
Granuloma, Respiratory Tract [MESH:D015769] (502) |
|
|
Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
|
|
Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
|
|
Hematoma [MESH:D006406] (281) |
|
|
Shock, Hemorrhagic [MESH:D012771] (2042) |
|
|
Peptic Ulcer Hemorrhage [MESH:D010438] (553) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2872) |
|
|
Subarachnoid Hemorrhage [MESH:D013345] (1081) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
|
|
|
Shock, Septic [MESH:D012772] (1830) |
|
|
Endotoxemia [MESH:D019446] (1289) |
|
|
Amenorrhea [MESH:D000568] (817) |
|
|
|
|
|
Choroidal Neovascularization [MESH:D020256] (550) |
|
|
Osteonecrosis [MESH:D010020] (537) |
|
|
Anaplasia [MESH:D000708] (348) |
|
|
Neoplasm Invasiveness [MESH:D009361] (3388) |
|
|
Neoplasm Recurrence, Local [MESH:D009364] (1949) |
|
|
Cell Transformation, Neoplastic [MESH:D002471] (3389) |
|
|
Lymphatic Metastasis [MESH:D008207] (917) |
|
|
|
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Multiple Organ Failure [MESH:D009102] (1836) |
|
|
Shock, Hemorrhagic [MESH:D012771] (2042) |
|
|
Shock, Septic [MESH:D012772] (1830) |
|
|
Chills [MESH:D023341] (644) |
|
|
Edema [MESH:D004487] (3726) |
|
|
Reticulocytosis [MESH:D045262] (514) |
|
|
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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Obesity, Morbid [MESH:D009767] (515) |
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Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
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Seizures [MESH:D012640] (4502) |
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Sleep Disorders [MESH:D012893] (1301) |
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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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Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
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Muscular Atrophy [MESH:D009133] (1234) |
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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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Gastroparesis [MESH:D018589] (732) |
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Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
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Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
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Hyperalgesia [MESH:D006930] (3929) |
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Paresthesia [MESH:D010292] (416) |
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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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Nausea [MESH:D009325] (2300) |
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Vomiting [MESH:D014839] (1354) |
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Anoxia [MESH:D000860] (1698) |
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Urinary Bladder, Overactive [MESH:D053201] (530) |
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Albuminuria [MESH:D000419] (2394) |
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C24. Occupational Diseases |
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C24. Occupational Diseases |
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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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Asthma, Aspirin-Induced [MESH:D055963] (1055) |
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Serum Sickness [MESH:D012713] (484) |
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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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Lead Poisoning [MESH:D007855] (515) |
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Manganese Poisoning [MESH:D020149] (2214) |
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Neurotoxicity Syndromes [MESH:D020258] (3323) |
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Psychoses, Substance-Induced [MESH:D011605] (2053) |
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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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Marijuana Abuse [MESH:D002189] (1132) |
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Phencyclidine Abuse [MESH:D010623] (288) |
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Psychoses, Substance-Induced [MESH:D011605] (2052) |
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Substance Withdrawal Syndrome [MESH:D013375] (2956) |
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Alcoholism [MESH:D000437] (1519) |
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Cardiomyopathy, Alcoholic [MESH:D002310] (354) |
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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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Morphine Dependence [MESH:D009021] (855) |
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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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Aortic Rupture [MESH:D001019] (637) |
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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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Onium Compounds [MESH:D009861] (1061) |
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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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Cardiofaciocutaneous syndrome [MESH:C535579] (407) |
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F. Psychiatry and Psychology |
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F. Psychiatry and Psychology |
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Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
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Parkinson Disease 4, Autosomal Dominant Lewy Body [MESH:C565324] (136) |
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Hoyeraal Hreidarsson syndrome [MESH:C536068] (154) |
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G. Phenomena and Processes |
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G. Phenomena and Processes |
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Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238) |
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Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238) |
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Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238) |
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Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238) |
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Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238) |
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Telomeric 22q13 Monosomy Syndrome [MESH:C536801] (238) |
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