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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ATP-binding cassette, sub-family C (CFTR/MRP), member 2 [HGNC:ABCC2] (152) |
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ATP-binding cassette, sub-family C (CFTR/MRP), member 3 [HGNC:ABCC3] (89) |
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ATP-binding cassette, sub-family C (CFTR/MRP), member 4 [HGNC:ABCC4] (88) |
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interleukin 06 (interferon, beta 2) [HGNC:IL6] (511) |
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interleukin 06 (interferon, beta 2) [HGNC:IL6] (511) |
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interleukin 10 [HGNC:IL10] (187) |
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solute carrier family 12 (potassium/chloride transporter), member 5 [HGNC:SLC12A5] (8) |
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solute carrier family 22 (organic anion transporter), member 08 [HGNC:SLC22A8] (42) |
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tumor necrosis factor [HGNC:TNF] (795) |
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UDP glucuronosyltransferase 1 family, polypeptide A1 [HGNC:UGT1A1] (167) |
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UDP glucuronosyltransferase 1 family, polypeptide A3 [HGNC:UGT1A3] (94) |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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abundance (136) |
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binding (2423) |
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transport (172) |
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activity (2549) |
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expression (2187) |
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reaction (3393) |
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secretion (346) |
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activity (2865) |
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expression (3238) |
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glucuronidation (189) |
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import (65) |
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reaction (1574) |
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transport (399) |
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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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Aortic Valve, Calcification of [MESH:C562942] (655) |
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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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Mycoplasma Infections [MESH:D009175] (1947) |
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Listeriosis [MESH:D008088] (1622) |
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Leprosy [MESH:D007918] (261) |
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Chlamydia Infections [MESH:D002690] (1693) |
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Arthritis, Infectious [MESH:D001170] (1702) |
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Corneal Ulcer [MESH:D003320] (61) |
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Appendicitis [MESH:D001064] (774) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Shock, Septic [MESH:D012772] (1830) |
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Chlamydia Infections [MESH:D002690] (1693) |
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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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Burkitt Lymphoma [MESH:D002051] (691) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Hepatitis B [MESH:D006509] (976) |
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Meningitis, Aseptic [MESH:D008582] (1305) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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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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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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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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Burkitt Lymphoma [MESH:D002051] (691) |
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C03. Parasitic Diseases |
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C03. Parasitic Diseases |
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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, Cutaneous [MESH:D016773] (2359) |
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Leishmaniasis, Visceral [MESH:D007898] (2149) |
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Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
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C04. Neoplasms |
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C04. Neoplasms |
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Neoplasms, Second Primary [MESH:D016609] (518) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Leukemia-Lymphoma, Adult T-Cell [MESH:D015459] (138) |
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032) |
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Leukemia, Megakaryoblastic, Acute [MESH:D007947] (279) |
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Leukemia, Promyelocytic, Acute [MESH:D015473] (1367) |
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Hodgkin Disease [MESH:D006689] (1082) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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Lymphoma, Follicular [MESH:D008224] (1025) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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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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Carcinosarcoma [MESH:D002296] (581) |
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Hepatoblastoma [MESH:D018197] (548) |
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Gastrointestinal Stromal Tumors [MESH:D046152] (170) |
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Sarcoma, Synovial [MESH:D013584] (993) |
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Chondrosarcoma, Mesenchymal [MESH:D018211] (1161) |
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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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Rhabdomyosarcoma [MESH:D012208] (789) |
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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, Synovial [MESH:D013584] (993) |
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Chondrosarcoma, Mesenchymal [MESH:D018211] (1161) |
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Rhabdomyosarcoma [MESH:D012208] (789) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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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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Vipoma [MESH:D003969] (110) |
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Pheochromocytoma [MESH:D010673] (275) |
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Mesothelioma [MESH:D008654] (2567) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Keratoacanthoma familial [MESH:C536150] (78) |
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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, 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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Vipoma [MESH:D003969] (110) |
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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, 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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Meningioma [MESH:D008579] (978) |
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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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Pheochromocytoma [MESH:D010673] (275) |
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Multiple Myeloma [MESH:D009101] (2767) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Meningioma [MESH:D008579] (978) |
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Hemangioma, capillary infantile [MESH:C535860] (190) |
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AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
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Melanoma [MESH:D008545] (3508) |
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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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Breast Neoplasms, Male [MESH:D018567] (650) |
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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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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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Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258) |
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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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Vipoma [MESH:D003969] (110) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Pituitary Neoplasms [MESH:D010911] (981) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Vipoma [MESH:D003969] (110) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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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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Salivary Gland Neoplasms [MESH:D012468] (968) |
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Tongue Neoplasms [MESH:D014062] (1518) |
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Bone Marrow Neoplasms [MESH:D019046] (91) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Pituitary Neoplasms [MESH:D010911] (914) |
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Meningioma [MESH:D008579] (978) |
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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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Vaginal Neoplasms [MESH:D014625] (363) |
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Endometrial Neoplasms [MESH:D016889] (1987) |
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Uterine Cervical Neoplasms [MESH:D002583] (978) |
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Prostate cancer, familial [MESH:C537243] (264) |
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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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Burkitt Lymphoma [MESH:D002051] (691) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Metastasis [MESH:D009362] (4441) |
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Neoplasm Recurrence, Local [MESH:D009364] (1949) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Hemangioma, capillary infantile [MESH:C535860] (190) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260) |
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Li-Fraumeni Syndrome [MESH:D016864] (859) |
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Leukoplakia, Oral [MESH:D007972] (921) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Bone Neoplasms [MESH:D001859] (1334) |
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Osteitis Deformans [MESH:D010001] (287) |
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Acromicric dysplasia [MESH:C535662] (520) |
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Marfan Syndrome [MESH:D008382] (646) |
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Camurati-Engelmann Syndrome [MESH:D003966] (492) |
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Fibrous Dysplasia of Bone [MESH:D005357] (737) |
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Osteogenesis Imperfecta [MESH:D010013] (481) |
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Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
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Osteopetrosis, Autosomal Recessive 7 [MESH:C567354] (36) |
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Acromegaly [MESH:D000172] (466) |
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Bone Demineralization, Pathologic [MESH:D018488] (5) |
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Rickets [MESH:D012279] (341) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Alveolar Bone Loss [MESH:D016301] (220) |
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Polyostotic osteolytic dysplasia, hereditary expansile [MESH:C536335] (36) |
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Intervertebral disc disease [MESH:C535531] (514) |
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Intervertebral disc disease [MESH:C535531] (514) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Spondylitis, Ankylosing [MESH:D013167] (431) |
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Cleft Palate [MESH:D002972] (1330) |
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Arthralgia [MESH:D018771] (191) |
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Spondylitis, Ankylosing [MESH:D013167] (431) |
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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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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Spondylitis, Ankylosing [MESH:D013167] (431) |
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Mitochondrial Myopathies [MESH:D017240] (2176) |
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Muscle Weakness [MESH:D018908] (478) |
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Rhabdomyolysis [MESH:D012206] (465) |
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Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
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Dermatomyositis [MESH:D003882] (1826) |
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Dermatomyositis [MESH:D003882] (1826) |
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Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107) |
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Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78) |
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Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107) |
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Cleft Palate [MESH:D002972] (1330) |
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Acromicric dysplasia [MESH:C535662] (520) |
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Arthritis, Juvenile [MESH:D001171] (1060) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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C06. Digestive System Diseases |
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C06. Digestive System Diseases |
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Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
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Gallbladder Neoplasms [MESH:D005706] (993) |
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Gallstones [MESH:D042882] (350) |
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Gallbladder Neoplasms [MESH:D005706] (993) |
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Gallstones [MESH:D042882] (350) |
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Barrett Esophagus [MESH:D001471] (1930) |
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Gallbladder Neoplasms [MESH:D005706] (993) |
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Gastrointestinal Stromal Tumors [MESH:D046152] (170) |
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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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Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258) |
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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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Vipoma [MESH:D003969] (110) |
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Barrett Esophagus [MESH:D001471] (1930) |
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Gastroesophageal Reflux [MESH:D005764] (1465) |
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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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Appendicitis [MESH:D001064] (774) |
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Enterocolitis [MESH:D004760] (1536) |
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Mucositis [MESH:D052016] (1238) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
|
|
Crohn Disease [MESH:D003424] (2585) |
|
|
Peptic Ulcer Hemorrhage [MESH:D010438] (553) |
|
|
Gastrointestinal Stromal Tumors [MESH:D046152] (170) |
|
|
Stomach Neoplasms [MESH:D013274] (4942) |
|
|
Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
|
|
Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
|
|
|
|
|
Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Enterocolitis [MESH:D004760] (1536) |
|
|
Intestinal Perforation [MESH:D007416] (471) |
|
|
Appendicitis [MESH:D001064] (774) |
|
|
|
|
|
Colitis, Ulcerative [MESH:D003093] (2601) |
|
|
Irritable Bowel Syndrome [MESH:D043183] (429) |
|
|
Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
|
|
|
Duodenal Ulcer [MESH:D004381] (1549) |
|
|
Colitis, Ulcerative [MESH:D003093] (2601) |
|
|
Crohn Disease [MESH:D003424] (2585) |
|
|
|
|
|
Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Colorectal Neoplasms [MESH:D015179] (4534) |
|
|
Duodenal Ulcer [MESH:D004381] (1549) |
|
|
Stomach Ulcer [MESH:D013276] (2915) |
|
|
Stomach Neoplasms [MESH:D013274] (4942) |
|
|
Stomach Ulcer [MESH:D013276] (2915) |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Hepatic Veno-Occlusive Disease [MESH:D006504] (208) |
|
|
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) |
|
|
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) |
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
Pancreatitis [MESH:D010195] (1924) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
Vipoma [MESH:D003969] (110) |
|
|
Peritoneal Fibrosis [MESH:D056627] (488) |
|
 |
C07. Stomatognathic Diseases |
 |
 |
|
C07. Stomatognathic Diseases |
|
|
|
|
|
|
|
|
|
|
|
PCI 5002 [MESH:C568608] (527) |
|
|
Periapical Periodontitis [MESH:D010485] (183) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Mucositis [MESH:D052016] (1238) |
|
|
Oral Submucous Fibrosis [MESH:D009914] (2432) |
|
|
|
|
|
PCI 5002 [MESH:C568608] (433) |
|
|
|
|
|
PCI 5002 [MESH:C568608] (433) |
|
|
Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535) |
|
|
Leukoplakia, Oral [MESH:D007972] (921) |
|
|
Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437) |
|
|
Orstavik Lindemann Solberg syndrome [MESH:C537137] (668) |
|
|
|
|
|
Periapical Periodontitis [MESH:D010485] (183) |
|
|
Alveolar Bone Loss [MESH:D016301] (220) |
|
|
Chronic Periodontitis [MESH:D055113] (231) |
|
|
Periapical Periodontitis [MESH:D010485] (183) |
|
|
|
|
|
Neuroendocrine Carcinoma of Salivary Glands, Sensorineural Hearing Loss, and Enamel Hypoplasia [MESH:C566352] (437) |
|
|
Stevens-Johnson Syndrome [MESH:D013262] (1163) |
|
|
|
|
|
Orstavik Lindemann Solberg syndrome [MESH:C537137] (668) |
|
|
|
|
|
|
|
|
|
|
|
Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535) |
|
|
|
|
|
Orofacial Cleft 12 [MESH:C567548] (434) |
|
|
Opitz GBBB Syndrome, X-Linked [MESH:C567932] (535) |
|
 |
C08. Respiratory Tract Diseases |
 |
 |
|
C08. Respiratory Tract Diseases |
|
|
Not Fully Specified [NFS] (1984) |
|
|
Respiratory System Abnormalities [MESH:D015619] (243) |
|
|
Bronchial Hyperreactivity [MESH:D016535] (1357) |
|
|
Bronchiectasis [MESH:D001987] (1792) |
|
|
Bronchopneumonia [MESH:D001996] (16) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Bronchitis, Chronic [MESH:D029481] (569) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
Hypertension, Pulmonary [MESH:D006976] (2000) |
|
|
Pulmonary Edema [MESH:D011654] (2109) |
|
|
Pulmonary Fibrosis [MESH:D011658] (3140) |
|
|
Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
|
|
|
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
Asthma [MESH:D001249] (3903) |
|
|
Bronchitis, Chronic [MESH:D029481] (569) |
|
|
Bronchitis, Chronic [MESH:D029481] (569) |
|
|
Pulmonary Emphysema [MESH:D011656] (1259) |
|
|
Acute Lung Injury [MESH:D055371] (1907) |
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
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) |
|
|
Bronchopneumonia [MESH:D001996] (16) |
|
|
|
|
|
Rhinitis, Allergic, Perennial [MESH:D012221] (625) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Dyspnea [MESH:D004417] (248) |
|
|
Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
|
|
Rhinitis, Allergic, Perennial [MESH:D012221] (625) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Influenza, Human [MESH:D007251] (1075) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Bronchitis, Chronic [MESH:D029481] (569) |
|
|
Bronchopneumonia [MESH:D001996] (16) |
|
|
|
|
|
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 |
|
|
|
|
|
|
|
|
Tinnitus [MESH:D014012] (109) |
|
|
Deafness [MESH:D003638] (623) |
|
|
Hearing Loss, Bilateral [MESH:D006312] (55) |
|
|
Pendred syndrome [MESH:C536648] (35) |
|
|
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness [MESH:C562897] (11) |
|
|
Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
|
|
Bartter Syndrome, Type 4A [MESH:C566530] (27) |
|
|
Bartter Syndrome, Type 4b [MESH:C567762] (14) |
|
|
Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92) |
|
|
Cochlear Diseases [MESH:D015834] (39) |
|
|
Vertigo [MESH:D014717] (97) |
|
|
|
|
|
|
|
|
Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92) |
|
|
|
|
|
Rhinitis, Allergic, Perennial [MESH:D012221] (625) |
|
|
Deglutition Disorders [MESH:D003680] (108) |
|
 |
C10. Nervous System Diseases |
 |
 |
|
C10. Nervous System Diseases |
|
|
Not Fully Specified [NFS] (4027) |
|
|
|
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
|
|
|
|
|
|
Hypotension, Orthostatic [MESH:D007024] (679) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3429) |
|
|
Hydrocephalus [MESH:D006849] (276) |
|
|
|
|
|
Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92) |
|
|
|
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
|
|
|
Cerebral Palsy, Spastic Quadriplegic, 1 [MESH:C567853] (99) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
Kernicterus [MESH:D007647] (256) |
|
|
Myelinolysis, Central Pontine [MESH:D017590] (7) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
|
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
|
|
|
|
|
|
Ataxia Telangiectasia [MESH:D001260] (142) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Ischemic Attack, Transient [MESH:D002546] (1313) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Moyamoya Disease [MESH:D009072] (10) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Moyamoya Disease [MESH:D009072] (10) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Status Epilepticus [MESH:D013226] (4014) |
|
|
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) |
|
|
Hyperprolactinemia [MESH:D006966] (603) |
|
|
Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28) |
|
|
Hydrocephalus [MESH:D006849] (274) |
|
|
|
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
|
|
|
|
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
Meningitis, Aseptic [MESH:D008582] (1305) |
|
|
|
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Spinal Cord Compression [MESH:D013117] (1800) |
|
|
Spinal Cord Injuries [MESH:D013119] (1674) |
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Amyotrophic Lateral Sclerosis 9 [MESH:C567499] (37) |
|
|
Myelinolysis, Central Pontine [MESH:D017590] (7) |
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
Knobloch syndrome [MESH:C537209] (70) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Pituitary Neoplasms [MESH:D010911] (914) |
|
|
Meningioma [MESH:D008579] (978) |
|
|
Ataxia Telangiectasia [MESH:D001260] (142) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Amyotrophic Lateral Sclerosis 9 [MESH:C567499] (37) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Amyotrophic Lateral Sclerosis 9 [MESH:C567499] (37) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
Seizures [MESH:D012640] (4514) |
|
|
Vertigo [MESH:D014717] (97) |
|
|
Catalepsy [MESH:D002375] (1429) |
|
|
Hyperkinesis [MESH:D006948] (1799) |
|
|
|
|
|
|
|
|
Ataxia Telangiectasia [MESH:D001260] (142) |
|
|
Lethargy [MESH:D053609] (1035) |
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
|
|
|
|
|
|
Dysarthria [MESH:D004401] (163) |
|
|
Delirium [MESH:D003693] (173) |
|
|
|
|
|
Coma [MESH:D003128] (524) |
|
|
Syncope [MESH:D013575] (128) |
|
|
Amnesia [MESH:D000647] (1911) |
|
|
Muscle Weakness [MESH:D018908] (478) |
|
|
Muscular Atrophy [MESH:D009133] (1234) |
|
|
Tetany [MESH:D013746] (23) |
|
|
Headache [MESH:D006261] (1416) |
|
|
Neuralgia [MESH:D009437] (2074) |
|
|
Low Back Pain [MESH:D017116] (244) |
|
|
Quadriplegia [MESH:D011782] (115) |
|
|
|
|
|
Tinnitus [MESH:D014012] (109) |
|
|
Deafness [MESH:D003638] (623) |
|
|
Hearing Loss, Bilateral [MESH:D006312] (55) |
|
|
Pendred syndrome [MESH:C536648] (35) |
|
|
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness [MESH:C562897] (11) |
|
|
Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
|
|
Bartter Syndrome, Type 4A [MESH:C566530] (27) |
|
|
Bartter Syndrome, Type 4b [MESH:C567762] (14) |
|
|
Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
Paresthesia [MESH:D010292] (416) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Amyotrophic Lateral Sclerosis 9 [MESH:C567499] (37) |
|
|
Mitochondrial Myopathies [MESH:D017240] (2176) |
|
|
|
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Diabetic Neuropathies [MESH:D003929] (2442) |
|
|
Neuralgia [MESH:D009437] (2078) |
|
|
Dyskinesia, Drug-Induced [MESH:D004409] (1389) |
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
|
|
|
Sleep Deprivation [MESH:D012892] (233) |
|
|
Spinal Cord Injuries [MESH:D013119] (1676) |
|
|
Brain Injuries [MESH:D001930] (3431) |
|
 |
C11. Eye Diseases |
 |
 |
|
C11. Eye Diseases |
|
|
Eye Abnormalities [MESH:D005124] (1233) |
|
|
Corneal Neovascularization [MESH:D016510] (622) |
|
|
Corneal Ulcer [MESH:D003320] (61) |
|
|
Corneal Ulcer [MESH:D003320] (61) |
|
|
Dry Eye Syndromes [MESH:D015352] (533) |
|
|
Cataract [MESH:D002386] (860) |
|
|
|
|
|
Glaucoma, Open-Angle [MESH:D005902] (1281) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
Retinal Vein Occlusion [MESH:D012170] (607) |
|
|
Retinopathy of Prematurity [MESH:D012178] (353) |
|
|
|
|
|
Macular Edema [MESH:D008269] (557) |
|
|
Knobloch syndrome [MESH:C537209] (70) |
|
|
|
|
|
Choroidal Neovascularization [MESH:D020256] (550) |
|
|
|
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C12. Male Urogenital Diseases |
 |
 |
|
C12. Male Urogenital Diseases |
|
|
|
|
|
Testicular Diseases [MESH:D013733] (451) |
|
|
|
|
|
Prostate cancer, familial [MESH:C537243] (264) |
|
|
|
|
|
Azoospermia [MESH:D053713] (1052) |
|
|
Penile Induration [MESH:D010411] (495) |
|
|
Prostatitis [MESH:D011472] (424) |
|
|
Prostate cancer, familial [MESH:C537243] (264) |
|
|
Erectile Dysfunction [MESH:D007172] (1791) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
Allanson Pantzar McLeod syndrome [MESH:C537048] (503) |
|
|
|
|
|
Cortisone reductase deficiency [MESH:C536447] (136) |
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
|
|
|
|
|
|
Prostate cancer, familial [MESH:C537243] (264) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Anuria [MESH:D001002] (833) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Kidney Diseases, Cystic [MESH:D052177] (1009) |
|
|
Diabetes Insipidus, Nephrogenic [MESH:D018500] (90) |
|
|
Hypertension, Renovascular [MESH:D006978] (365) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
Glomerulonephritis, Membranous [MESH:D015433] (642) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Hypomagnesemia primary [MESH:C537153] (35) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Nephrosis, Lipoid [MESH:D009402] (74) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Hypomagnesemia primary [MESH:C537153] (35) |
|
|
Liddle Syndrome [MESH:D056929] (200) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness [MESH:C562897] (11) |
|
|
Bartter syndrome, antenatal type 1 [MESH:C537652] (39) |
|
|
Bartter Syndrome, Type 4A [MESH:C566530] (27) |
|
|
Bartter Syndrome, Type 4b [MESH:C567762] (14) |
|
|
Azotemia [MESH:D053099] (326) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Ureteral Obstruction [MESH:D014517] (575) |
|
|
|
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Cystitis [MESH:D003556] (604) |
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Anuria [MESH:D001002] (833) |
|
|
Hematuria [MESH:D006417] (477) |
|
|
Oliguria [MESH:D009846] (307) |
|
|
Polyuria [MESH:D011141] (279) |
|
|
Urinary Incontinence [MESH:D014549] (81) |
|
|
Nocturnal Enuresis [MESH:D053206] (15) |
|
|
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 |
|
|
Not Fully Specified [NFS] (1116) |
|
|
|
|
|
Endometriosis [MESH:D004715] (2461) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
Uterine Cervical Neoplasms [MESH:D002583] (978) |
|
|
Endometrial Neoplasms [MESH:D016889] (1984) |
|
|
Uterine Cervical Neoplasms [MESH:D002583] (978) |
|
|
Vaginal Neoplasms [MESH:D014625] (363) |
|
|
Allanson Pantzar McLeod syndrome [MESH:C537048] (503) |
|
|
|
|
|
Cortisone reductase deficiency [MESH:C536447] (136) |
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Vaginal Neoplasms [MESH:D014625] (363) |
|
|
Endometrial Neoplasms [MESH:D016889] (1989) |
|
|
Uterine Cervical Neoplasms [MESH:D002583] (978) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Anuria [MESH:D001002] (833) |
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Kidney Diseases, Cystic [MESH:D052177] (1009) |
|
|
Diabetes Insipidus, Nephrogenic [MESH:D018500] (90) |
|
|
Hypertension, Renovascular [MESH:D006978] (365) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
Glomerulonephritis, Membranous [MESH:D015433] (642) |
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Hypomagnesemia primary [MESH:C537153] (35) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Nephrosis, Lipoid [MESH:D009402] (74) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Hypomagnesemia primary [MESH:C537153] (35) |
|
|
Liddle Syndrome [MESH:D056929] (200) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness [MESH:C562897] (11) |
|
|
Bartter syndrome, antenatal type 1 [MESH:C537652] (39) |
|
|
Bartter Syndrome, Type 4A [MESH:C566530] (27) |
|
|
Bartter Syndrome, Type 4b [MESH:C567762] (14) |
|
|
Azotemia [MESH:D053099] (326) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Ureteral Obstruction [MESH:D014517] (575) |
|
|
|
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Cystitis [MESH:D003556] (604) |
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Anuria [MESH:D001002] (833) |
|
|
Hematuria [MESH:D006417] (477) |
|
|
Oliguria [MESH:D009846] (307) |
|
|
Polyuria [MESH:D011141] (279) |
|
|
Urinary Incontinence [MESH:D014549] (81) |
|
|
Nocturnal Enuresis [MESH:D053206] (15) |
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
|
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Diabetes, Gestational [MESH:D016640] (1157) |
|
|
Fetal Death [MESH:D005313] (464) |
|
|
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) |
|
|
Prenatal Exposure Delayed Effects [MESH:D011297] (870) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
|
|
|
Ductus Arteriosus, Patent [MESH:D004374] (325) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
|
|
|
Venous Malformations, Multiple Cutaneous and Mucosal [MESH:C563977] (62) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Cardiac Output, Low [MESH:D002303] (31) |
|
|
Heart Arrest [MESH:D006323] (1926) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Pericardial Effusion [MESH:D010490] (1015) |
|
|
Bradycardia [MESH:D001919] (1899) |
|
|
Atrial Fibrillation, Familial, 6 [MESH:C567400] (196) |
|
|
Ventricular Premature Complexes [MESH:D018879] (418) |
|
|
Atrioventricular Block [MESH:D054537] (188) |
|
|
Tachycardia, Supraventricular [MESH:D013617] (199) |
|
|
Torsades de Pointes [MESH:D016171] (880) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
|
|
Hypertrophy, Right Ventricular [MESH:D017380] (136) |
|
|
Cardiomyopathy, Alcoholic [MESH:D002310] (354) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Endomyocardial Fibrosis [MESH:D004719] (521) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocarditis [MESH:D009205] (1708) |
|
|
Ductus Arteriosus, Patent [MESH:D004374] (325) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Aortic Valve Insufficiency [MESH:D001022] (1002) |
|
|
Mitral Valve Insufficiency [MESH:D008944] (35) |
|
|
Aortic Valve, Calcification of [MESH:C562942] (655) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
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) |
|
|
Shock, Cardiogenic [MESH:D012770] (269) |
|
|
Ventricular Dysfunction, Left [MESH:D018487] (1631) |
|
|
|
|
|
Aortic Valve, Calcification of [MESH:C562942] (655) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
Hepatic Veno-Occlusive Disease [MESH:D006504] (208) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Retinal Vein Occlusion [MESH:D012170] (607) |
|
|
Vascular System Injuries [MESH:D057772] (2086) |
|
|
|
|
|
|
|
|
Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107) |
|
|
Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78) |
|
|
Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107) |
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107) |
|
|
Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78) |
|
|
Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107) |
|
|
Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107) |
|
|
Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78) |
|
|
Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107) |
|
|
Aortitis [MESH:D001025] (4) |
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107) |
|
|
Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78) |
|
|
Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107) |
|
|
Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107) |
|
|
Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78) |
|
|
Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107) |
|
|
Moyamoya Disease [MESH:D009072] (10) |
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Venous Malformations, Multiple Cutaneous and Mucosal [MESH:C563977] (62) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
|
|
|
Ischemic Attack, Transient [MESH:D002546] (1313) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Moyamoya Disease [MESH:D009072] (10) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Moyamoya Disease [MESH:D009072] (10) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
|
|
|
|
|
|
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, Pregnancy-Induced [MESH:D046110] (397) |
|
|
Hypertension, Renovascular [MESH:D006978] (365) |
|
|
Hypotension, Orthostatic [MESH:D007024] (679) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
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) |
|
|
No-Reflow Phenomenon [MESH:D054318] (277) |
|
|
Shock, Cardiogenic [MESH:D012770] (269) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Ataxia Telangiectasia [MESH:D001260] (142) |
|
|
Aortitis [MESH:D001025] (4) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158) |
|
|
Vasculitis, Leukocytoclastic, Cutaneous [MESH:D018366] (121) |
|
 |
C15. Hemic and Lymphatic Diseases |
 |
 |
|
C15. Hemic and Lymphatic Diseases |
|
|
Pancytopenia [MESH:D010198] (332) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Purpura [MESH:D011693] (475) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
|
|
|
Kernicterus [MESH:D007647] (256) |
|
|
|
|
|
|
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
|
|
|
Osteopetrosis, Autosomal Recessive 7 [MESH:C567354] (36) |
|
|
Hypoalbuminemia [MESH:D034141] (1332) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Bone Marrow Neoplasms [MESH:D019046] (91) |
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
Myeloproliferative Disorder, Chronic, with Eosinophilia [MESH:C565054] (134) |
|
|
Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Bone Marrow Neoplasms [MESH:D019046] (91) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Thrombocythemia, Essential [MESH:D013920] (707) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
Myeloproliferative Disorder, Chronic, with Eosinophilia [MESH:C565054] (134) |
|
|
Hypereosinophilic Syndrome [MESH:D017681] (119) |
|
|
|
|
|
Neutropenia [MESH:D009503] (1629) |
|
|
Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158) |
|
|
Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
|
|
Giant Lymph Node Hyperplasia [MESH:D005871] (1013) |
|
|
Granuloma [MESH:D006099] (72) |
|
|
Sarcoidosis [MESH:D012507] (895) |
|
|
Osteopetrosis, Autosomal Recessive 7 [MESH:C567354] (36) |
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Leukemia-Lymphoma, Adult T-Cell [MESH:D015459] (138) |
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
|
Burkitt Lymphoma [MESH:D002051] (691) |
|
|
Lymphoma, Follicular [MESH:D008224] (1025) |
|
|
Burkitt Lymphoma [MESH:D002051] (691) |
|
|
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 |
|
|
|
|
|
Eye Abnormalities [MESH:D005124] (1233) |
|
|
Respiratory System Abnormalities [MESH:D015619] (244) |
|
|
Skin Abnormalities [MESH:D012868] (1723) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107) |
|
|
Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78) |
|
|
Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107) |
|
|
|
|
|
Ductus Arteriosus, Patent [MESH:D004374] (325) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
|
|
|
Venous Malformations, Multiple Cutaneous and Mucosal [MESH:C563977] (62) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
|
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Acromicric dysplasia [MESH:C535662] (520) |
|
|
|
|
|
Intracranial Arteriovenous Malformations [MESH:D002538] (1015) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
Knobloch syndrome [MESH:C537209] (70) |
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Allanson Pantzar McLeod syndrome [MESH:C537048] (503) |
|
|
|
|
|
Cortisone reductase deficiency [MESH:C536447] (136) |
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
Fetal Growth Retardation [MESH:D005317] (986) |
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
Ataxia Telangiectasia [MESH:D001260] (142) |
|
|
Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
|
|
Camurati-Engelmann Syndrome [MESH:D003966] (492) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Osteogenesis Imperfecta [MESH:D010013] (481) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Periodic fever, familial, autosomal dominant [MESH:C536657] (177) |
|
|
Aortic aneurysm, familial thoracic 3 [MESH:C537783] (107) |
|
|
Loeys-Dietz Syndrome, Type 2A [MESH:C567156] (78) |
|
|
Loeys-Dietz Syndrome, Type 1b [MESH:C567181] (107) |
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254) |
|
|
Gilbert Disease [MESH:D005878] (259) |
|
|
Jaundice, Chronic Idiopathic [MESH:D007566] (287) |
|
|
Crigler Najjar syndrome, type 2 [MESH:C536213] (254) |
|
|
Hyperlipidemia, Familial Combined [MESH:D006950] (372) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
Hypomagnesemia primary [MESH:C537153] (35) |
|
|
Liddle Syndrome [MESH:D056929] (200) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness [MESH:C562897] (11) |
|
|
Cortisone reductase deficiency [MESH:C536447] (136) |
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Hemangioma, capillary infantile [MESH:C535860] (190) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (260) |
|
|
Li-Fraumeni Syndrome [MESH:D016864] (859) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
Asphyxia Neonatorum [MESH:D001238] (1648) |
|
|
Cystic Fibrosis [MESH:D003550] (760) |
|
|
Kernicterus [MESH:D007647] (256) |
|
|
Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254) |
|
|
Jaundice, Chronic Idiopathic [MESH:D007566] (287) |
|
|
Bronchopulmonary Dysplasia [MESH:D001997] (1021) |
|
|
Retinopathy of Prematurity [MESH:D012178] (353) |
|
 |
C17. Skin and Connective Tissue Diseases |
 |
 |
|
C17. Skin and Connective Tissue Diseases |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
|
|
Marfan Syndrome [MESH:D008382] (646) |
|
|
Penile Induration [MESH:D010411] (495) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Keloid [MESH:D007627] (1111) |
|
|
Osteogenesis Imperfecta [MESH:D010013] (481) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Hand Dermatoses [MESH:D006229] (25) |
|
|
Keratosis [MESH:D007642] (1941) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Skin Abnormalities [MESH:D012868] (1709) |
|
|
Skin Neoplasms [MESH:D012878] (2991) |
|
|
Chloracne [MESH:D054506] (1274) |
|
|
|
|
|
Breast Neoplasms, Male [MESH:D018567] (650) |
|
|
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) |
|
|
|
|
|
Cortisone reductase deficiency [MESH:C536447] (136) |
|
|
Keratoacanthoma familial [MESH:C536150] (78) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Periodic fever, familial, autosomal dominant [MESH:C536657] (177) |
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
|
|
|
Leishmaniasis, Cutaneous [MESH:D016773] (2359) |
|
|
|
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
Lichenoid Eruptions [MESH:D017512] (1324) |
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Mucocutaneous Lymph Node Syndrome [MESH:D009080] (158) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
|
|
|
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) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness [MESH:C562897] (11) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
Kernicterus [MESH:D007647] (256) |
|
|
Myelinolysis, Central Pontine [MESH:D017590] (7) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Rickets [MESH:D012279] (341) |
|
|
Aortic Valve, Calcification of [MESH:C562942] (655) |
|
|
Hypomagnesemia primary [MESH:C537153] (35) |
|
|
Tetany [MESH:D013746] (23) |
|
|
Ataxia Telangiectasia [MESH:D001260] (142) |
|
|
Colorectal Neoplasms, Hereditary Nonpolyposis [MESH:D003123] (258) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Li-Fraumeni Syndrome [MESH:D016864] (859) |
|
|
Hyperglycemia [MESH:D006943] (1858) |
|
|
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) |
|
|
|
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
|
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
|
|
|
|
|
|
Hypercholesterolemia [MESH:D006937] (1404) |
|
|
Hyperlipidemia, Familial Combined [MESH:D006950] (372) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
|
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254) |
|
|
Gilbert Disease [MESH:D005878] (259) |
|
|
Jaundice, Chronic Idiopathic [MESH:D007566] (287) |
|
|
Crigler Najjar syndrome, type 2 [MESH:C536213] (254) |
|
|
Hyperlipidemia, Familial Combined [MESH:D006950] (372) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
Hypomagnesemia primary [MESH:C537153] (35) |
|
|
Liddle Syndrome [MESH:D056929] (200) |
|
|
Osteopetrosis with renal tubular acidosis [MESH:C536058] (130) |
|
|
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness [MESH:C562897] (11) |
|
|
Cortisone reductase deficiency [MESH:C536447] (136) |
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
Mitochondrial Myopathies [MESH:D017240] (2176) |
|
|
Hyperphosphatemia [MESH:D054559] (159) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Amyotrophic Lateral Sclerosis 9 [MESH:C567499] (37) |
|
|
|
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Dehydration [MESH:D003681] (121) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Hyperkalemia [MESH:D006947] (485) |
|
|
Hypocalcemia [MESH:D006996] (368) |
|
|
Hypokalemia [MESH:D007008] (1041) |
|
|
Hyponatremia [MESH:D007010] (789) |
|
|
Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
Rickets [MESH:D012279] (341) |
|
|
|
|
|
Obesity, Abdominal [MESH:D056128] (115) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
Bone Diseases, Endocrine [MESH:D001849] (173) |
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
|
|
|
|
|
|
Bartter syndrome, antenatal type 1 [MESH:C537652] (39) |
|
|
Bartter Syndrome, Type 4A [MESH:C566530] (27) |
|
|
Bartter Syndrome, Type 4b [MESH:C567762] (14) |
|
|
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) |
|
|
Pituitary Neoplasms [MESH:D010911] (981) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
Vipoma [MESH:D003969] (110) |
|
|
Puberty, Precocious [MESH:D011629] (1147) |
|
|
Testicular Diseases [MESH:D013733] (777) |
|
|
|
|
|
Cortisone reductase deficiency [MESH:C536447] (136) |
|
|
Adrenal Hyperplasia, Congenital [MESH:D000312] (674) |
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
|
|
|
Hyperparathyroidism, Secondary [MESH:D006962] (1138) |
|
|
Hypoparathyroidism familial isolated [MESH:C537156] (108) |
|
|
Pituitary Neoplasms [MESH:D010911] (981) |
|
|
Acromegaly [MESH:D000172] (466) |
|
|
Hyperprolactinemia [MESH:D006966] (603) |
|
|
Nephrogenic Syndrome of Inappropriate Antidiuresis [MESH:C564491] (28) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
|
|
|
Pendred syndrome [MESH:C536648] (35) |
|
|
Hyperthyroxinemia, Familial Dysalbuminemic [MESH:D050010] (478) |
|
 |
C20. Immune System Diseases |
 |
 |
|
C20. Immune System Diseases |
|
|
Glomerulonephritis, Membranoproliferative [MESH:D015432] (770) |
|
|
Arthritis, Juvenile [MESH:D001171] (1060) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1893) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Glomerulonephritis, Membranous [MESH:D015433] (642) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
Encephalomyelitis, Autoimmune, Experimental [MESH:D004681] (806) |
|
|
|
|
|
Kernicterus [MESH:D007647] (256) |
|
|
|
|
|
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) |
|
|
Asthma [MESH:D001249] (3914) |
|
|
Rhinitis, Allergic, Perennial [MESH:D012221] (625) |
|
|
Angioedema [MESH:D000799] (837) |
|
|
Serum Sickness [MESH:D012713] (484) |
|
|
Vasculitis, Leukocytoclastic, Cutaneous [MESH:D018366] (121) |
|
|
Ataxia Telangiectasia [MESH:D001260] (142) |
|
|
Osteopetrosis, Autosomal Recessive 7 [MESH:C567354] (36) |
|
|
Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
|
|
HIV Seropositivity [MESH:D006679] (480) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
AIDS-related Kaposi sarcoma [MESH:C554498] (914) |
|
|
|
|
|
Autoimmune Lymphoproliferative Syndrome [MESH:D056735] (704) |
|
|
Giant Lymph Node Hyperplasia [MESH:D005871] (1013) |
|
|
Multiple Myeloma [MESH:D009101] (2767) |
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Leukemia-Lymphoma, Adult T-Cell [MESH:D015459] (138) |
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
|
Burkitt Lymphoma [MESH:D002051] (691) |
|
|
Lymphoma, Follicular [MESH:D008224] (1025) |
|
|
Burkitt Lymphoma [MESH:D002051] (691) |
|
|
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) |
|
 |
C23. Pathological Conditions, Signs and Symptoms |
 |
 |
|
C23. Pathological Conditions, Signs and Symptoms |
|
|
Dilatation, Pathologic [MESH:D004108] (11) |
|
|
Ventricular Remodeling [MESH:D020257] (686) |
|
|
Muscular Atrophy [MESH:D009133] (1234) |
|
|
Gallstones [MESH:D042882] (350) |
|
|
Kidney Calculi [MESH:D007669] (455) |
|
|
Hernia, Diaphragmatic [MESH:D006548] (2647) |
|
|
Knobloch syndrome [MESH:C537209] (70) |
|
|
Hernia, Inguinal [MESH:D006552] (111) |
|
|
Intervertebral disc disease [MESH:C535531] (514) |
|
|
|
|
|
Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
|
|
Hypertrophy, Right Ventricular [MESH:D017380] (136) |
|
|
Leukoplakia, Oral [MESH:D007972] (921) |
|
|
Intestinal Polyps [MESH:D007417] (1592) |
|
|
Ascites [MESH:D001201] (139) |
|
|
Azotemia [MESH:D053099] (326) |
|
|
Dehydration [MESH:D003681] (121) |
|
|
Emphysema [MESH:D004646] (1096) |
|
|
Gliosis [MESH:D005911] (1419) |
|
|
Granuloma [MESH:D006099] (587) |
|
|
Hyperplasia [MESH:D006965] (2463) |
|
|
Hypovolemia [MESH:D020896] (12) |
|
|
Muscle Weakness [MESH:D018908] (478) |
|
|
Neointima [MESH:D058426] (814) |
|
|
Nerve Degeneration [MESH:D009410] (4061) |
|
|
Bradycardia [MESH:D001919] (1899) |
|
|
Atrial Fibrillation, Familial, 6 [MESH:C567400] (196) |
|
|
Ventricular Premature Complexes [MESH:D018879] (418) |
|
|
Atrioventricular Block [MESH:D054537] (188) |
|
|
Tachycardia, Supraventricular [MESH:D013617] (199) |
|
|
Torsades de Pointes [MESH:D016171] (880) |
|
|
Death, Sudden [MESH:D003645] (725) |
|
|
Fetal Death [MESH:D005313] (464) |
|
|
Disease Progression [MESH:D018450] (2868) |
|
|
Genetic Predisposition to Disease [MESH:D020022] (966) |
|
|
Peritoneal Fibrosis [MESH:D056627] (488) |
|
|
Keloid [MESH:D007627] (1110) |
|
|
Microsatellite Instability [MESH:D053842] (141) |
|
|
Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
|
|
Fetal Growth Retardation [MESH:D005317] (986) |
|
|
Hematuria [MESH:D006417] (477) |
|
|
Purpura [MESH:D011693] (475) |
|
|
Shock, Hemorrhagic [MESH:D012771] (2042) |
|
|
Peptic Ulcer Hemorrhage [MESH:D010438] (553) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2872) |
|
|
Kernicterus [MESH:D007647] (256) |
|
|
Hyperbilirubinemia, Transient Familial Neonatal [MESH:C562692] (254) |
|
|
Acute-Phase Reaction [MESH:D000210] (40) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
|
|
|
Shock, Septic [MESH:D012772] (1830) |
|
|
Infarction [MESH:D007238] (298) |
|
|
No-Reflow Phenomenon [MESH:D054318] (277) |
|
|
|
|
|
Choroidal Neovascularization [MESH:D020256] (550) |
|
|
Infarction [MESH:D007238] (298) |
|
|
Neoplasm Invasiveness [MESH:D009361] (3388) |
|
|
Neoplasm Metastasis [MESH:D009362] (4441) |
|
|
Neoplasm Recurrence, Local [MESH:D009364] (1949) |
|
|
Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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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, Cardiogenic [MESH:D012770] (269) |
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Shock, Hemorrhagic [MESH:D012771] (2042) |
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Shock, Septic [MESH:D012772] (1830) |
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Cardiac Output, Low [MESH:D002303] (31) |
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Cyanosis [MESH:D003490] (288) |
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Edema [MESH:D004487] (3726) |
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Fatigue [MESH:D005221] (437) |
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Flushing [MESH:D005483] (506) |
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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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Obesity [MESH:D009765] (4454) |
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Seizures [MESH:D012640] (4502) |
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Vertigo [MESH:D014717] (97) |
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Ataxia [MESH:D001259] (984) |
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Catalepsy [MESH:D002375] (1429) |
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Hyperkinesis [MESH:D006948] (1799) |
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Lethargy [MESH:D053609] (1035) |
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Learning Disorders [MESH:D007859] (2727) |
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Dysarthria [MESH:D004401] (163) |
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Delirium [MESH:D003693] (173) |
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Coma [MESH:D003128] (492) |
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Syncope [MESH:D013575] (128) |
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Amnesia [MESH:D000647] (1911) |
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Muscle Weakness [MESH:D018908] (478) |
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Muscular Atrophy [MESH:D009133] (1234) |
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Tetany [MESH:D013746] (23) |
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Headache [MESH:D006261] (1417) |
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Neuralgia [MESH:D009437] (2074) |
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Low Back Pain [MESH:D017116] (244) |
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Quadriplegia [MESH:D011782] (115) |
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Tinnitus [MESH:D014012] (109) |
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Deafness [MESH:D003638] (593) |
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Hearing Loss, Bilateral [MESH:D006312] (55) |
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Pendred syndrome [MESH:C536648] (35) |
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Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness [MESH:C562897] (11) |
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Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
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Bartter Syndrome, Type 4A [MESH:C566530] (27) |
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Bartter Syndrome, Type 4b [MESH:C567762] (14) |
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Auditory Neuropathy, Autosomal Dominant, 1 [MESH:C563790] (92) |
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Hyperalgesia [MESH:D006930] (3929) |
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Paresthesia [MESH:D010292] (416) |
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Sleep Deprivation [MESH:D012892] (233) |
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Abdominal Pain [MESH:D015746] (248) |
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Arthralgia [MESH:D018771] (191) |
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Headache [MESH:D006261] (1417) |
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Neuralgia [MESH:D009437] (2074) |
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Low Back Pain [MESH:D017116] (244) |
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Acute Coronary Syndrome [MESH:D054058] (2286) |
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Angina, Stable [MESH:D060050] (1702) |
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Abdominal Pain [MESH:D015746] (248) |
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Anorexia [MESH:D000855] (854) |
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Diarrhea [MESH:D003967] (858) |
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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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Dyspnea [MESH:D004417] (248) |
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Hypercapnia [MESH:D006935] (264) |
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Hyperoxia [MESH:D018496] (694) |
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Respiratory Sounds [MESH:D012135] (713) |
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Purpura [MESH:D011693] (475) |
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Oliguria [MESH:D009846] (307) |
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Polyuria [MESH:D011141] (279) |
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Urinoma [MESH:D053584] (2) |
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Hypomagnesemia primary [MESH:C537153] (35) |
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Urinary Incontinence [MESH:D014549] (81) |
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Albuminuria [MESH:D000419] (2394) |
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Cortisone reductase deficiency [MESH:C536447] (136) |
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C24. Occupational Diseases |
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C24. Occupational Diseases |
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Berylliosis [MESH:D001607] (2005) |
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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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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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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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Marijuana Abuse [MESH:D002189] (1132) |
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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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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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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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Fractures, Bone [MESH:D050723] (597) |
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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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Furosemide [MESH:D005665] (9) |
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Furosemide [MESH:D005665] (9) |
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Furosemide [MESH:D005665] (9) |
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F. Psychiatry and Psychology |
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F. Psychiatry and Psychology |
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Cortisone reductase deficiency [MESH:C536447] (136) |
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G. Phenomena and Processes |
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G. Phenomena and Processes |
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Polyostotic osteolytic dysplasia, hereditary expansile [MESH:C536335] (36) |
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