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 G (WHITE), member 1 [HGNC:ABCG1] (40) |
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FBJ murine osteosarcoma viral oncogene homolog [HGNC:FOS] (277) |
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cholesteryl ester transfer protein, plasma [HGNC:CETP] (17) |
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atypical chemokine receptor 3 [HGNC:ACKR3] (35) |
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intercellular adhesion molecule 1 [HGNC:ICAM1] (286) |
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selectin E [HGNC:SELE] (94) |
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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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atypical chemokine receptor 3 [HGNC:ACKR3] (35) |
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chemokine (C-C motif) ligand 02 [HGNC:CCL2] (337) |
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chemokine (C-X-C motif) ligand 01 (melanoma growth stimulating activity, alpha) [HGNC:CXCL1] (82) |
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chemokine (C-X-C motif) ligand 02 [HGNC:CXCL2] (65) |
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chemokine (C-X-C motif) ligand 11 [HGNC:CXCL11] (22) |
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interleukin 08 [HGNC:IL8] (649) |
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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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interferon, gamma [HGNC:IFNG] (274) |
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interleukin 01, alpha [HGNC:IL1A] (157) |
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interleukin 08 [HGNC:IL8] (649) |
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estrogen receptor 1 [HGNC:ESR1] (506) |
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estrogen receptor 2 (ER beta) [HGNC:ESR2] (261) |
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nuclear receptor subfamily 1, group H, member 2 [HGNC:NR1H2] (22) |
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nuclear receptor subfamily 5, group A, member 1 [HGNC:NR5A1] (21) |
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signal transducer and activator of transcription 1, 91kDa [HGNC:STAT1] (108) |
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NAD(P) dependent steroid dehydrogenase-like [HGNC:NSDHL] (8) |
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steroidogenic acute regulatory protein [HGNC:STAR] (57) |
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interferon-induced protein with tetratricopeptide repeats 2 [HGNC:IFIT2] (31) |
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tumor necrosis factor [HGNC:TNF] (795) |
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tumor necrosis factor (ligand) superfamily, member 15 [HGNC:TNFSF15] (13) |
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early growth response 1 [HGNC:EGR1] (140) |
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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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activity (2865) |
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expression (3238) |
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localization (244) |
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phosphorylation (1060) |
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reaction (1574) |
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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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Listeriosis [MESH:D008088] (1622) |
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Mycobacterium Infections, Nontuberculous [MESH:D009165] (480) |
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Tuberculosis, Pulmonary [MESH:D014397] (678) |
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Chlamydia Infections [MESH:D002690] (1693) |
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Arthritis, Infectious [MESH:D001170] (1702) |
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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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Chlamydia Infections [MESH:D002690] (1693) |
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Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
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Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
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Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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Hepatitis B [MESH:D006509] (976) |
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Cytomegalovirus Infections [MESH:D003586] (222) |
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Hepatitis B [MESH:D006509] (976) |
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Hepatitis C [MESH:D006526] (1627) |
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Hepatitis C [MESH:D006526] (1627) |
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Respiratory Syncytial Virus Infections [MESH:D018357] (852) |
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Influenza, Human [MESH:D007251] (1075) |
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Cardiovirus Infections [MESH:D018188] (1548) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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HIV Wasting Syndrome [MESH:D019247] (1956) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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C03. Parasitic Diseases |
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C03. Parasitic Diseases |
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Trichuriasis [MESH:D014257] (805) |
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Malaria [MESH:D008288] (2175) |
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Entamoebiasis [MESH:D004749] (1689) |
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Leishmaniasis, Visceral [MESH:D007898] (2149) |
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Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
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Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
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C04. Neoplasms |
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C04. Neoplasms |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Leukemia, Promyelocytic, Acute [MESH:D015473] (1367) |
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Lymphoma, B-Cell [MESH:D016393] (2624) |
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Chondrosarcoma, Mesenchymal [MESH:D018211] (1161) |
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Mastocytosis, Systemic [MESH:D034721] (769) |
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Fibromatosis, Aggressive [MESH:D018222] (1562) |
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Leiomyoma [MESH:D007889] (744) |
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Leiomyosarcoma [MESH:D007890] (977) |
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Leiomyosarcoma [MESH:D007890] (977) |
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Chondrosarcoma, Mesenchymal [MESH:D018211] (1161) |
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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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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, Transitional Cell [MESH:D002295] (2662) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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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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Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565) |
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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, Ductal, Breast [MESH:D018270] (1112) |
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Mesothelioma [MESH:D008654] (2567) |
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Medulloblastoma [MESH:D008527] (1282) |
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Glioblastoma [MESH:D005909] (2554) |
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Medulloblastoma [MESH:D008527] (1282) |
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Papilloma [MESH:D010212] (2243) |
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Carcinoma, squamous cell of head and neck [MESH:C535575] (1543) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Medulloblastoma [MESH:D008527] (1282) |
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Glioblastoma [MESH:D005909] (2554) |
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Medulloblastoma [MESH:D008527] (1282) |
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Melanoma [MESH:D008545] (3508) |
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Multiple Myeloma [MESH:D009101] (2767) |
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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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Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Adenocarcinoma Of Esophagus [MESH:C562730] (1530) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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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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Tongue Neoplasms [MESH:D014062] (1518) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Endometrial Neoplasms [MESH:D016889] (1987) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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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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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Tuberous Sclerosis [MESH:D014402] (635) |
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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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Bone Neoplasms [MESH:D001859] (1334) |
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Fibrous Dysplasia of Bone [MESH:D005357] (737) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Osteolysis [MESH:D010014] (1787) |
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Arthritis, Psoriatic [MESH:D015535] (1859) |
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Cleft Palate [MESH:D002972] (1330) |
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Arthralgia [MESH:D018771] (191) |
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Arthritis, Experimental [MESH:D001169] (3142) |
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Arthritis, Infectious [MESH:D001170] (1702) |
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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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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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Dermatomyositis [MESH:D003882] (1826) |
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Dermatomyositis [MESH:D003882] (1826) |
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Cleft Palate [MESH:D002972] (1330) |
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Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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Osteoarthritis [MESH:D010003] (1743) |
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C06. Digestive System Diseases |
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C06. Digestive System Diseases |
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Cholestasis, Intrahepatic [MESH:D002780] (1510) |
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Gallstones [MESH:D042882] (350) |
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Gallstones [MESH:D042882] (350) |
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Barrett Esophagus [MESH:D001471] (1930) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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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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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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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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Esophagitis, Peptic [MESH:D004942] (709) |
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Appendicitis [MESH:D001064] (774) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Esophagitis, Peptic [MESH:D004942] (709) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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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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Intestinal Perforation [MESH:D007416] (471) |
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Appendicitis [MESH:D001064] (774) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Adenomatous Polyposis Coli [MESH:D011125] (1565) |
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Colorectal Neoplasms [MESH:D015179] (4534) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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Esophagitis, Peptic [MESH:D004942] (709) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Gastroparesis [MESH:D018589] (732) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Cholestasis, Intrahepatic [MESH:D002780] (1510) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Hepatorenal Syndrome [MESH:D006530] (910) |
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Hypertension, Portal [MESH:D006975] (869) |
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Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567) |
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Hepatic Encephalopathy [MESH:D006501] (1795) |
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Liver Failure, Acute [MESH:D017114] (2404) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Hepatitis, Autoimmune [MESH:D019693] (1982) |
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Hepatitis B [MESH:D006509] (976) |
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Hepatitis C [MESH:D006526] (1627) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
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Hepatitis, Alcoholic [MESH:D006519] (1613) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Pancreatitis [MESH:D010195] (1924) |
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Peritonitis [MESH:D010538] (800) |
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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Cleft Palate [MESH:D002972] (1330) |
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Behcet Syndrome [MESH:D001528] (1784) |
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Oral Submucous Fibrosis [MESH:D009914] (2432) |
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Cleft Lip [MESH:D002971] (914) |
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Cleft Lip [MESH:D002971] (914) |
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Cleft Palate [MESH:D002972] (1330) |
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Leukoplakia, Oral [MESH:D007972] (921) |
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Tongue Neoplasms [MESH:D014062] (1518) |
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Tongue Neoplasms [MESH:D014062] (1518) |
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Cleft Palate [MESH:D002972] (1330) |
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Cleft Lip [MESH:D002971] (914) |
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Cleft Palate [MESH:D002972] (1330) |
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C08. Respiratory Tract Diseases |
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C08. Respiratory Tract Diseases |
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Not Fully Specified [NFS] (1984) |
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Bronchial Hyperreactivity [MESH:D016535] (1357) |
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Bronchiectasis [MESH:D001987] (1792) |
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Asthma, Aspirin-Induced [MESH:D055963] (1055) |
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Bronchiolitis Obliterans [MESH:D001989] (611) |
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Hypertension, Pulmonary [MESH:D006976] (2000) |
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Pneumonia [MESH:D011014] (3482) |
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Pulmonary Edema [MESH:D011654] (2109) |
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Pulmonary Fibrosis [MESH:D011658] (3140) |
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Tuberculosis, Pulmonary [MESH:D014397] (678) |
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Anthracosis [MESH:D055008] (1805) |
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Berylliosis [MESH:D001607] (2005) |
|
|
Asthma [MESH:D001249] (3903) |
|
|
|
|
|
Bronchiolitis Obliterans [MESH:D001989] (611) |
|
|
Pulmonary Emphysema [MESH:D011656] (1259) |
|
|
Acute Lung Injury [MESH:D055371] (1907) |
|
|
Anthracosis [MESH:D055008] (1805) |
|
|
Berylliosis [MESH:D001607] (2005) |
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
|
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Influenza, Human [MESH:D007251] (1075) |
|
|
Pleurisy [MESH:D010998] (2070) |
|
|
Pneumonia [MESH:D011014] (3482) |
|
|
Tuberculosis, Pulmonary [MESH:D014397] (678) |
|
|
Legionnaires' Disease [MESH:D007877] (611) |
|
|
|
|
|
|
|
|
|
|
|
Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
|
 |
C09. Otorhinolaryngologic Diseases |
 |
 |
|
C09. Otorhinolaryngologic Diseases |
|
|
|
|
|
|
|
|
Hearing Loss [MESH:D034381] (2068) |
|
|
Vestibular Diseases [MESH:D015837] (819) |
|
 |
C10. Nervous System Diseases |
 |
 |
|
C10. Nervous System Diseases |
|
|
Not Fully Specified [NFS] (4027) |
|
|
|
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3429) |
|
|
|
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Mevalonate Kinase Deficiency [MESH:D054078] (38) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
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) |
|
|
|
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
|
|
|
Migraine Disorders [MESH:D008881] (2318) |
|
|
|
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Spinal Cord Compression [MESH:D013117] (1800) |
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
|
|
|
|
|
|
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) |
|
|
|
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Meningomyelocele [MESH:D008591] (100) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Parkinson Disease [MESH:D010300] (3595) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Alzheimer Disease [MESH:D000544] (4275) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
Seizures [MESH:D012640] (4514) |
|
|
Hyperkinesis [MESH:D006948] (1799) |
|
|
|
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
Amnesia [MESH:D000647] (1911) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Pain, Intractable [MESH:D010148] (707) |
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
|
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
|
|
|
Hearing Loss [MESH:D034381] (2068) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
|
|
|
|
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
|
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
|
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
Tangier Disease [MESH:D013631] (170) |
|
|
|
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3431) |
|
 |
C11. Eye Diseases |
 |
 |
|
C11. Eye Diseases |
|
|
Eyelid Diseases [MESH:D005141] (882) |
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Cataract, Pulverulent, Juvenile-Onset [MESH:C565703] (69) |
|
|
|
|
|
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) |
|
|
|
|
|
|
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
|
|
|
|
|
|
|
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C12. Male Urogenital Diseases |
 |
 |
|
C12. Male Urogenital Diseases |
|
|
|
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
|
|
|
Oligospermia [MESH:D009845] (799) |
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Erectile Dysfunction [MESH:D007172] (1791) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
|
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
|
|
|
Prostatic Neoplasms [MESH:D011471] (6135) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Nephrosis [MESH:D009401] (2228) |
|
|
Hypertension, Renovascular [MESH:D006978] (365) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
|
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Cystitis, Interstitial [MESH:D018856] (264) |
|
|
|
|
|
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) |
|
|
Premature Ovarian Failure 7 [MESH:C567838] (52) |
|
|
|
|
|
Chlamydia Infections [MESH:D002690] (1693) |
|
|
|
|
|
Endometrial Neoplasms [MESH:D016889] (1984) |
|
|
|
|
|
|
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Endometrial Neoplasms [MESH:D016889] (1989) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Diabetic Nephropathies [MESH:D003928] (2301) |
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Hydronephrosis [MESH:D006869] (956) |
|
|
Hyperoxaluria [MESH:D006959] (1498) |
|
|
Nephrosis [MESH:D009401] (2228) |
|
|
Hypertension, Renovascular [MESH:D006978] (365) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Nephritis, Interstitial [MESH:D009395] (1927) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
|
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neck Obstruction [MESH:D001748] (924) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Cystitis, Interstitial [MESH:D018856] (264) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Chorioamnionitis [MESH:D002821] (313) |
|
|
Pre-Eclampsia [MESH:D011225] (1435) |
|
|
Abruptio Placentae [MESH:D000037] (430) |
|
|
Obstetric Labor, Premature [MESH:D007752] (1316) |
|
|
Chorioamnionitis [MESH:D002821] (313) |
|
|
Abruptio Placentae [MESH:D000037] (430) |
|
|
Chorioamnionitis [MESH:D002821] (313) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
Pregnancy Complications, Cardiovascular [MESH:D011249] (1994) |
|
|
Cardiomegaly [MESH:D006332] (4081) |
|
|
Heart Arrest [MESH:D006323] (1926) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Heart Valve Diseases [MESH:D006349] (3333) |
|
|
Pericardial Effusion [MESH:D010490] (1015) |
|
|
Ventricular Dysfunction [MESH:D018754] (2348) |
|
|
Atrial Fibrillation [MESH:D001281] (1053) |
|
|
Ventricular Premature Complexes [MESH:D018879] (418) |
|
|
Tachycardia, Ventricular [MESH:D017180] (1386) |
|
|
Diabetic Cardiomyopathies [MESH:D058065] (1995) |
|
|
Kearns-Sayre Syndrome [MESH:D007625] (1054) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocarditis [MESH:D009205] (1708) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Unstable [MESH:D000789] (782) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Vasospasm [MESH:D003329] (533) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Hypotension [MESH:D007022] (4045) |
|
|
Vascular System Injuries [MESH:D057772] (2086) |
|
|
|
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
|
|
|
Aortic Aneurysm, Abdominal [MESH:D017544] (1519) |
|
|
|
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Diabetic Retinopathy [MESH:D003930] (1371) |
|
|
Thrombosis [MESH:D013927] (3101) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Hypertension, Essential [MESH:C562386] (1308) |
|
|
Hypertension, Pregnancy-Induced [MESH:D046110] (397) |
|
|
Hypertension, Renovascular [MESH:D006978] (365) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Unstable [MESH:D000789] (782) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Vasospasm [MESH:D003329] (533) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Stunning [MESH:D017682] (1816) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
 |
C15. Hemic and Lymphatic Diseases |
 |
 |
|
C15. Hemic and Lymphatic Diseases |
|
|
Blood Coagulation Disorders [MESH:D001778] (1828) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
|
|
|
|
|
|
Hemolytic-Uremic Syndrome [MESH:D006463] (2435) |
|
|
|
|
|
Mevalonate Kinase Deficiency [MESH:D054078] (38) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
|
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Anemia, Refractory [MESH:D000753] (1567) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Leukostasis [MESH:D018921] (769) |
|
|
Job Syndrome [MESH:D007589] (772) |
|
|
|
|
|
|
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
|
|
|
Lymphoma, B-Cell [MESH:D016393] (2624) |
|
 |
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
 |
 |
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
|
|
|
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Smith-Lemli-Opitz Syndrome [MESH:D019082] (100) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
|
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45) |
|
|
|
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Meningomyelocele [MESH:D008591] (100) |
|
|
Spinal Dysraphism [MESH:D016135] (1025) |
|
|
|
|
|
|
|
|
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45) |
|
|
|
|
|
|
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
Cleft Lip [MESH:D002971] (914) |
|
|
Cleft Palate [MESH:D002972] (1330) |
|
|
|
|
|
|
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
Chorioamnionitis [MESH:D002821] (313) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
|
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Anemia, Sickle Cell [MESH:D000755] (1722) |
|
|
Mevalonate Kinase Deficiency [MESH:D054078] (38) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Optic Atrophy, Hereditary, Leber [MESH:D029242] (1100) |
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Mevalonate Kinase Deficiency [MESH:D054078] (38) |
|
|
Hyperlipidemia, Familial Combined [MESH:D006950] (372) |
|
|
Hyperlipoproteinemia Type I [MESH:D008072] (219) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
Lipidoses [MESH:D008064] (1655) |
|
|
Smith-Lemli-Opitz Syndrome [MESH:D019082] (100) |
|
|
|
|
|
Familial HDL deficiency [MESH:C538394] (170) |
|
|
Tangier Disease [MESH:D013631] (170) |
|
|
Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Mevalonate Kinase Deficiency [MESH:D054078] (38) |
|
|
Smith-Lemli-Opitz Syndrome [MESH:D019082] (100) |
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
|
|
Adenomatous Polyposis Coli [MESH:D011125] (1565) |
|
|
Tuberous Sclerosis [MESH:D014402] (635) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45) |
|
|
Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52) |
|
|
Asphyxia Neonatorum [MESH:D001238] (1648) |
|
|
|
|
|
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45) |
|
 |
C17. Skin and Connective Tissue Diseases |
 |
 |
|
C17. Skin and Connective Tissue Diseases |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Dermatomyositis [MESH:D003882] (1826) |
|
|
Exanthema [MESH:D005076] (301) |
|
|
Scleroderma, Localized [MESH:D012594] (1597) |
|
|
Skin Neoplasms [MESH:D012878] (2991) |
|
|
|
|
|
Carcinoma, Ductal, Breast [MESH:D018270] (1112) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
|
|
|
|
|
|
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45) |
|
|
Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52) |
|
|
|
|
|
|
|
|
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects [MESH:C562515] (45) |
|
|
Porokeratosis, disseminated superficial actinic 1 [MESH:C536339] (52) |
|
|
|
|
|
Candidiasis, Chronic Mucocutaneous [MESH:D002178] (224) |
|
|
|
|
|
|
|
|
Leishmaniasis, Mucocutaneous [MESH:D007897] (606) |
|
|
|
|
|
Lipodystrophy, Familial Partial [MESH:D052496] (589) |
|
|
Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145) |
|
|
Lichenoid Eruptions [MESH:D017512] (1324) |
|
|
Arthritis, Psoriatic [MESH:D015535] (1859) |
|
|
Behcet Syndrome [MESH:D001528] (1784) |
|
|
Urticaria [MESH:D014581] (2668) |
|
|
Pemphigoid, Bullous [MESH:D010391] (707) |
|
 |
C18. Nutritional and Metabolic Diseases |
 |
 |
|
C18. Nutritional and Metabolic Diseases |
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Mevalonate Kinase Deficiency [MESH:D054078] (38) |
|
|
Calcinosis [MESH:D002114] (2989) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Fanconi Anemia [MESH:D005199] (1604) |
|
|
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) |
|
|
|
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
|
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Lipidoses [MESH:D008064] (1655) |
|
|
Smith-Lemli-Opitz Syndrome [MESH:D019082] (100) |
|
|
Hypercholesterolemia [MESH:D006937] (1404) |
|
|
Hyperlipidemia, Familial Combined [MESH:D006950] (372) |
|
|
Hypertriglyceridemia [MESH:D015228] (808) |
|
|
Hyperlipoproteinemia Type I [MESH:D008072] (219) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
|
|
|
Familial HDL deficiency [MESH:C538394] (170) |
|
|
Tangier Disease [MESH:D013631] (170) |
|
|
Lipodystrophy, Familial Partial [MESH:D052496] (589) |
|
|
Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145) |
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1724) |
|
|
MELAS Syndrome [MESH:D017241] (1061) |
|
|
MERRF Syndrome [MESH:D017243] (1053) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Mevalonate Kinase Deficiency [MESH:D054078] (38) |
|
|
Hyperlipidemia, Familial Combined [MESH:D006950] (372) |
|
|
Hyperlipoproteinemia Type I [MESH:D008072] (219) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
Lipidoses [MESH:D008064] (1655) |
|
|
Smith-Lemli-Opitz Syndrome [MESH:D019082] (100) |
|
|
|
|
|
Familial HDL deficiency [MESH:C538394] (170) |
|
|
Tangier Disease [MESH:D013631] (170) |
|
|
Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145) |
|
|
Hemochromatosis [MESH:D006432] (1694) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Mevalonate Kinase Deficiency [MESH:D054078] (38) |
|
|
Smith-Lemli-Opitz Syndrome [MESH:D019082] (100) |
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
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) |
|
|
|
|
|
Lipodystrophy, Familial Partial [MESH:D052496] (589) |
|
|
Lipodystrophy, Congenital Generalized, Type 3 [MESH:C567282] (145) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Hypercalcemia [MESH:D006934] (1999) |
|
|
Hyponatremia [MESH:D007010] (789) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Hyperhomocysteinemia [MESH:D020138] (1716) |
|
|
Obesity [MESH:D009765] (4462) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
|
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
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 Retinopathy [MESH:D003930] (1371) |
|
|
Ovarian Neoplasms [MESH:D010051] (3275) |
|
|
Pancreatic Neoplasms [MESH:D010190] (3820) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
Puberty, Precocious [MESH:D011629] (1147) |
|
|
|
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Gonadal Dysgenesis, 46,XX [MESH:D023961] (56) |
|
|
Gonadal Dysgenesis, 46,XY [MESH:D006061] (131) |
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
Premature Ovarian Failure 7 [MESH:C567838] (52) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
 |
C20. Immune System Diseases |
 |
 |
|
C20. Immune System Diseases |
|
|
Graft vs Host Disease [MESH:D006086] (674) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Diabetes Mellitus, Type 1 [MESH:D003922] (1893) |
|
|
Glomerulonephritis, IGA [MESH:D005922] (897) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
Lupus Erythematosus, Systemic [MESH:D008180] (2317) |
|
|
Pemphigoid, Bullous [MESH:D010391] (707) |
|
|
|
|
|
Multiple Sclerosis [MESH:D009103] (1716) |
|
|
|
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Dermatitis, Atopic [MESH:D003876] (2052) |
|
|
Urticaria [MESH:D014581] (2668) |
|
|
Asthma [MESH:D001249] (3914) |
|
|
|
|
|
Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
|
|
HIV Wasting Syndrome [MESH:D019247] (1956) |
|
|
Job Syndrome [MESH:D007589] (772) |
|
|
|
|
|
Mevalonate Kinase Deficiency [MESH:D054078] (38) |
|
|
Multiple Myeloma [MESH:D009101] (2767) |
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
|
|
|
Lymphoma, B-Cell [MESH:D016393] (2624) |
|
|
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 |
|
|
|
|
|
Gallstones [MESH:D042882] (350) |
|
|
Hernia, Diaphragmatic [MESH:D006548] (2647) |
|
|
Cardiomegaly [MESH:D006332] (3802) |
|
|
Leukoplakia, Oral [MESH:D007972] (921) |
|
|
Intestinal Polyps [MESH:D007417] (1592) |
|
|
Fibrosis [MESH:D005355] (3133) |
|
|
Growth Disorders [MESH:D006130] (2438) |
|
|
Hyperbilirubinemia [MESH:D006932] (1860) |
|
|
Hyperplasia [MESH:D006965] (2463) |
|
|
Ischemia [MESH:D007511] (3049) |
|
|
Lithiasis [MESH:D020347] (345) |
|
|
Necrosis [MESH:D009336] (4019) |
|
|
Nerve Degeneration [MESH:D009410] (4061) |
|
|
Atrial Fibrillation [MESH:D001281] (1053) |
|
|
Ventricular Premature Complexes [MESH:D018879] (418) |
|
|
Tachycardia, Ventricular [MESH:D017180] (1386) |
|
|
Disease Progression [MESH:D018450] (2868) |
|
|
Shock, Hemorrhagic [MESH:D012771] (2042) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2872) |
|
|
Neurogenic Inflammation [MESH:D020078] (2246) |
|
|
|
|
|
Shock, Septic [MESH:D012772] (1830) |
|
|
Neoplasm Invasiveness [MESH:D009361] (3388) |
|
|
Neoplasm Metastasis [MESH:D009362] (4441) |
|
|
Neoplasm Recurrence, Local [MESH:D009364] (1949) |
|
|
Cell Transformation, Neoplastic [MESH:D002471] (3389) |
|
|
|
|
|
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) |
|
|
Feminization [MESH:D005262] (655) |
|
|
Fever [MESH:D005334] (2856) |
|
|
Hypothermia [MESH:D007035] (2075) |
|
|
|
|
|
Weight Gain [MESH:D015430] (2595) |
|
|
|
|
|
Cachexia [MESH:D002100] (2283) |
|
|
Obesity [MESH:D009765] (4454) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Hyperkinesis [MESH:D006948] (1799) |
|
|
|
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
Amnesia [MESH:D000647] (1911) |
|
|
Pain, Intractable [MESH:D010148] (707) |
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
Gastroparesis [MESH:D018589] (732) |
|
|
Ophthalmoplegia, Chronic Progressive External [MESH:D017246] (1311) |
|
|
|
|
|
Hearing Loss [MESH:D034381] (2066) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
Arthralgia [MESH:D018771] (191) |
|
|
Pain, Intractable [MESH:D010148] (707) |
|
|
|
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Angina, Unstable [MESH:D000789] (782) |
|
|
Angina, Stable [MESH:D060050] (1702) |
|
|
Neuralgia, Postherpetic [MESH:D051474] (742) |
|
|
Diarrhea [MESH:D003967] (858) |
|
|
Nausea [MESH:D009325] (2300) |
|
|
Vomiting [MESH:D014839] (1354) |
|
|
Anoxia [MESH:D000860] (1698) |
|
|
|
|
|
Albuminuria [MESH:D000419] (2394) |
|
 |
C24. Occupational Diseases |
 |
 |
|
C24. Occupational Diseases |
|
|
|
|
|
Berylliosis [MESH:D001607] (2005) |
|
 |
C25. Chemically-Induced Disorders |
 |
 |
|
C25. Chemically-Induced Disorders |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Asthma, Aspirin-Induced [MESH:D055963] (1055) |
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Manganese Poisoning [MESH:D020149] (2214) |
|
|
Neurotoxicity Syndromes [MESH:D020258] (3323) |
|
|
Psychoses, Substance-Induced [MESH:D011605] (2053) |
|
|
Amphetamine-Related Disorders [MESH:D019969] (2858) |
|
|
Cocaine-Related Disorders [MESH:D019970] (3054) |
|
|
Marijuana Abuse [MESH:D002189] (1132) |
|
|
Phencyclidine Abuse [MESH:D010623] (288) |
|
|
Psychoses, Substance-Induced [MESH:D011605] (2052) |
|
|
Substance Withdrawal Syndrome [MESH:D013375] (2956) |
|
|
|
|
|
|
|
|
Hepatitis, Alcoholic [MESH:D006519] (1613) |
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
 |
C26. Wounds and Injuries |
 |
 |
|
C26. Wounds and Injuries |
|
|
Not Fully Specified [NFS] (2454) |
|
|
Burns [MESH:D002056] (2565) |
|
|
Vascular System Injuries [MESH:D057772] (2086) |
|
|
Brain Injuries [MESH:D001930] (3431) |
|
|
Radiation Injuries, Experimental [MESH:D011833] (2662) |
|
|
Spinal Cord Compression [MESH:D013117] (1800) |
|
|
Lung Injury [MESH:D055370] (1814) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3431) |
|
 |
D04. Polycyclic Compounds |
 |
 |
|
D04. Polycyclic Compounds |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Hydroxycholesterols [MESH:D006888] (42) |
|
|
|
|
|
Hydroxycholesterols [MESH:D006888] (42) |
|
 |
D10. Lipids |
 |
 |
|
D10. Lipids |
|
|
|
|
|
|
|
|
|
|
|
Hydroxycholesterols [MESH:D006888] (42) |
|
 |
F. Psychiatry and Psychology |
 |
 |
|
F. Psychiatry and Psychology |
|
|
|
|
|
|
|
|
|
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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