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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MAX dimerization protein 1 [HGNC:MXD1] (46) |
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insulin-like growth factor 1 receptor [HGNC:IGF1R] (72) |
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cyclin-dependent kinase 02 [HGNC:CDK2] (177) |
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cytochrome P450, family 01, subfamily A, polypeptide 02 [HGNC:CYP1A2] (466) |
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adiponectin, C1Q and collagen domain containing [HGNC:ADIPOQ] (71) |
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coagulation factor II (thrombin) [HGNC:F2] (95) |
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insulin-like growth factor 1 receptor [HGNC:IGF1R] (72) |
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gamma-aminobutyric acid (GABA) A receptor, alpha 1 [HGNC:GABRA1] (57) |
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gamma-aminobutyric acid (GABA) A receptor, beta 2 [HGNC:GABRB2] (37) |
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gamma-aminobutyric acid (GABA) A receptor, gamma 2 [HGNC:GABRG2] (58) |
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glutathione S-transferase pi 1 [HGNC:GSTP1] (218) |
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heat shock protein 90kDa alpha (cytosolic), class B member 1 [HGNC:HSP90AB1] (30) |
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fms-related tyrosine kinase 4 [HGNC:FLT4] (11) |
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fms-related tyrosine kinase 4 [HGNC:FLT4] (11) |
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interleukin 01 receptor antagonist [HGNC:IL1RN] (58) |
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interleukin 02 [HGNC:IL2] (144) |
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interleukin 12A (natural killer cell stimulatory factor 1, cytotoxic lymphocyte maturation factor 1, p35) [HGNC:IL12A] (77) |
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orosomucoid 1 [HGNC:ORM1] (20) |
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MAX dimerization protein 1 [HGNC:MXD1] (46) |
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mitogen-activated protein kinase 01 [HGNC:MAPK1] (651) |
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mitogen-activated protein kinase 03 [HGNC:MAPK3] (644) |
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nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor) [HGNC:NR3C1] (138) |
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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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expression (494) |
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localization (731) |
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abundance (224) |
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phosphorylation (590) |
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reaction (3393) |
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activity (2865) |
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expression (3238) |
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phosphorylation (1060) |
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4. Semantic Terms |
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4. Semantic Terms |
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Organic Chemical [STY:T109] (44144) |
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A. Anatomy |
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A. Anatomy |
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Coffin-Siris syndrome [MESH:C536436] (102) |
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Coffin-Siris syndrome [MESH:C536436] (102) |
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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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Paratuberculosis [MESH:D010283] (427) |
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Sepsis [MESH:D018805] (3556) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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Hepatitis C [MESH:D006526] (1627) |
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Hepatitis C [MESH:D006526] (1627) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
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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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Entamoebiasis [MESH:D004749] (1689) |
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C04. Neoplasms |
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C04. Neoplasms |
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Hamartoma [MESH:D006222] (1484) |
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Precancerous Conditions [MESH:D011230] (2858) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032) |
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Hodgkin Disease [MESH:D006689] (1082) |
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Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23) |
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Osteosarcoma [MESH:D012516] (2175) |
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Osteosarcoma [MESH:D012516] (2175) |
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Glioblastoma [MESH:D005909] (2554) |
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Melanoma [MESH:D008545] (3508) |
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Pancreatic cancer, adult [MESH:C535836] (572) |
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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565) |
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Glioblastoma [MESH:D005909] (2554) |
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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Glioblastoma [MESH:D005909] (2554) |
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Melanoma [MESH:D008545] (3508) |
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Multiple Myeloma [MESH:D009101] (2767) |
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Hemangioma, capillary infantile [MESH:C535860] (190) |
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Melanoma [MESH:D008545] (3508) |
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Head and Neck Neoplasms [MESH:D006258] (4612) |
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Skin Neoplasms [MESH:D012878] (2992) |
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Breast Neoplasms, Male [MESH:D018567] (650) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Pancreatic cancer, adult [MESH:C535836] (572) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Pancreatic cancer, adult [MESH:C535836] (572) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Vaginal Neoplasms [MESH:D014625] (363) |
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Endometrial Neoplasms [MESH:D016889] (1987) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Ureteral Neoplasms [MESH:D014516] (574) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23) |
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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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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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Neoplasm, Residual [MESH:D018365] (478) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Hemangioma, capillary infantile [MESH:C535860] (190) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Bone Resorption [MESH:D001862] (2352) |
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Kyphosis [MESH:D007738] (637) |
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Coffin-Siris syndrome [MESH:C536436] (102) |
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Coffin-Siris syndrome [MESH:C536436] (102) |
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Arthritis, Experimental [MESH:D001169] (3142) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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Myositis [MESH:D009220] (2071) |
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Minicore Myopathy with External Ophthalmoplegia [MESH:C564969] (51) |
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Myopathy, Central Core [MESH:D020512] (54) |
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Coffin-Siris syndrome [MESH:C536436] (102) |
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Coffin-Siris syndrome [MESH:C536436] (102) |
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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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Stomach Neoplasms [MESH:D013274] (4942) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Pancreatic cancer, adult [MESH:C535836] (572) |
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Mucositis [MESH:D052016] (1238) |
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Crohn Disease [MESH:D003424] (2585) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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Crohn Disease [MESH:D003424] (2585) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Colorectal Neoplasms [MESH:D015179] (4534) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Hepatomegaly [MESH:D006529] (1169) |
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Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
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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, Autoimmune [MESH:D019693] (1982) |
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Hepatitis C [MESH:D006526] (1627) |
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Liver Cirrhosis, Biliary [MESH:D008105] (1274) |
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Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Porphyria Cutanea Tarda [MESH:D017119] (766) |
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Pancreatitis [MESH:D010195] (1924) |
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Pancreatic cancer, adult [MESH:C535836] (572) |
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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Coffin-Siris syndrome [MESH:C536436] (102) |
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Mucositis [MESH:D052016] (1238) |
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Coffin-Siris syndrome [MESH:C536436] (102) |
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C08. Respiratory Tract Diseases |
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C08. Respiratory Tract Diseases |
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Asthma [MESH:D001249] (4098) |
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Bronchial Hyperreactivity [MESH:D016535] (1357) |
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Pneumonia [MESH:D011014] (3482) |
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Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
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Anthracosis [MESH:D055008] (1805) |
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Silicosis [MESH:D012829] (1273) |
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Asthma [MESH:D001249] (3903) |
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Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564) |
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Anthracosis [MESH:D055008] (1805) |
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Silicosis [MESH:D012829] (1273) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Hyperventilation [MESH:D006985] (654) |
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Respiratory Distress Syndrome, Adult [MESH:D012128] (864) |
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Respiratory Insufficiency [MESH:D012131] (841) |
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Asthma [MESH:D001249] (4098) |
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Pneumonia [MESH:D011014] (3482) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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C09. Otorhinolaryngologic Diseases |
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C09. Otorhinolaryngologic Diseases |
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Hearing Loss [MESH:D034381] (2068) |
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Vestibular Diseases [MESH:D015837] (819) |
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C10. Nervous System Diseases |
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C10. Nervous System Diseases |
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Chronobiology Disorders [MESH:D021081] (970) |
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Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170) |
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Brain Injuries [MESH:D001930] (3429) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Lewy Body Disease [MESH:D020961] (1143) |
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Parkinson Disease [MESH:D010300] (3595) |
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Hepatic Encephalopathy [MESH:D006501] (1795) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
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Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23) |
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Cerebral Infarction [MESH:D002544] (2458) |
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Carotid Stenosis [MESH:D016893] (174) |
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Cerebral Amyloid Angiopathy [MESH:D016657] (470) |
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Sinus Thrombosis, Intracranial [MESH:D012851] (356) |
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Cerebral Infarction [MESH:D002544] (2458) |
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Lewy Body Disease [MESH:D020961] (1143) |
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Alzheimer disease type 2 [MESH:C536595] (165) |
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Landau-Kleffner Syndrome [MESH:D018887] (87) |
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Seizures [MESH:D012640] (4502) |
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Status Epilepticus [MESH:D013226] (4014) |
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Myoclonic Epilepsy, Juvenile [MESH:D020190] (166) |
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Epilepsy, Rolandic [MESH:D019305] (107) |
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Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170) |
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Generalized Epilepsy With Febrile Seizures Plus, Type 3 [MESH:C565811] (102) |
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Epilepsy, Absence [MESH:D004832] (222) |
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Generalized Epilepsy With Febrile Seizures Plus, Type 1 [MESH:C565809] (170) |
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Generalized Epilepsy With Febrile Seizures Plus, Type 3 [MESH:C565811] (102) |
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Essential Tremor [MESH:D020329] (235) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Lewy Body Disease [MESH:D020961] (1143) |
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Parkinson Disease [MESH:D010300] (3595) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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Minicore Myopathy with External Ophthalmoplegia [MESH:C564969] (51) |
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Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170) |
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Neural Tube Defects [MESH:D009436] (2143) |
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Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23) |
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Lewy Body Disease [MESH:D020961] (1143) |
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Parkinson Disease [MESH:D010300] (3595) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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Alzheimer disease type 2 [MESH:C536595] (165) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Pain [MESH:D010146] (3875) |
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Reflex, Abnormal [MESH:D012021] (485) |
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Seizures [MESH:D012640] (4514) |
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Ataxia [MESH:D001259] (1138) |
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Hyperkinesis [MESH:D006948] (1799) |
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Language Development Disorders [MESH:D007805] (351) |
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Speech Disorders [MESH:D013064] (482) |
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Amnesia [MESH:D000647] (1911) |
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Coffin-Siris syndrome [MESH:C536436] (102) |
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Minicore Myopathy with External Ophthalmoplegia [MESH:C564969] (51) |
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Hearing Loss [MESH:D034381] (2068) |
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Hyperalgesia [MESH:D006930] (3929) |
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Peripheral Nervous System Diseases [MESH:D010523] (6151) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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Myositis [MESH:D009220] (2069) |
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Minicore Myopathy with External Ophthalmoplegia [MESH:C564969] (51) |
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Myopathy, Central Core [MESH:D020512] (54) |
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Arsenic Poisoning [MESH:D020261] (2540) |
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Brain Injuries [MESH:D001930] (3431) |
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C11. Eye Diseases |
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C11. Eye Diseases |
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Ocular Hypertension [MESH:D009798] (1630) |
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Minicore Myopathy with External Ophthalmoplegia [MESH:C564969] (51) |
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Macular Degeneration, Age-Related, 1 [MESH:C566411] (276) |
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C12. Male Urogenital Diseases |
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C12. Male Urogenital Diseases |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Infertility, Male [MESH:D007248] (2851) |
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Hypospadias 1, X-Linked [MESH:C567482] (571) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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46, XX Disorders of Sex Development [MESH:D058489] (644) |
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Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
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Hypospadias 1, X-Linked [MESH:C567482] (571) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Ureteral Neoplasms [MESH:D014516] (574) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Lipoprotein Glomerulopathy [MESH:C567089] (165) |
|
|
Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Glomerulonephritis [MESH:D005921] (3758) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Ureteral Neoplasms [MESH:D014516] (574) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Proteinuria [MESH:D011507] (3293) |
|
 |
C13. Female Urogenital Diseases and Pregnancy Complications |
 |
 |
|
C13. Female Urogenital Diseases and Pregnancy Complications |
|
|
|
|
|
Endometriosis [MESH:D004715] (2461) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
Infertility, Female [MESH:D007247] (2184) |
|
|
|
|
|
Endometrial Neoplasms [MESH:D016889] (1984) |
|
|
Vaginal Neoplasms [MESH:D014625] (363) |
|
|
|
|
|
46, XX Disorders of Sex Development [MESH:D058489] (644) |
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Vaginal Neoplasms [MESH:D014625] (363) |
|
|
Endometrial Neoplasms [MESH:D016889] (1989) |
|
|
Ureteral Neoplasms [MESH:D014516] (574) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Lipoprotein Glomerulopathy [MESH:C567089] (165) |
|
|
Rhabdoid Tumor Predisposition Syndrome 1 [MESH:C563738] (23) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
Glomerulonephritis [MESH:D005921] (3758) |
|
|
Nephrotic Syndrome [MESH:D009404] (1536) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Ureteral Neoplasms [MESH:D014516] (574) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Proteinuria [MESH:D011507] (3293) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Diabetes, Gestational [MESH:D016640] (1157) |
|
|
Fetal Growth Retardation [MESH:D005317] (986) |
|
|
Prenatal Exposure Delayed Effects [MESH:D011297] (870) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
Not Fully Specified [NFS] (2667) |
|
|
|
|
|
Heart Defects, Congenital [MESH:D006330] (2447) |
|
|
Cardiomegaly [MESH:D006332] (4081) |
|
|
Heart Defects, Congenital [MESH:D006330] (2443) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Tachycardia [MESH:D013610] (3339) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Infarction [MESH:D009203] (4122) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Arteritis [MESH:D001167] (1084) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Hypertension [MESH:D006973] (5655) |
|
|
Hypotension [MESH:D007022] (4045) |
|
|
Peripheral Vascular Diseases [MESH:D016491] (1412) |
|
|
Carotid Stenosis [MESH:D016893] (174) |
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
|
|
|
|
|
|
Cerebral Infarction [MESH:D002544] (2458) |
|
|
Carotid Stenosis [MESH:D016893] (174) |
|
|
|
|
|
Cerebral Amyloid Angiopathy [MESH:D016657] (470) |
|
|
|
|
|
Sinus Thrombosis, Intracranial [MESH:D012851] (356) |
|
|
|
|
|
Cerebral Infarction [MESH:D002544] (2458) |
|
|
|
|
|
Venous Thromboembolism [MESH:D054556] (400) |
|
|
|
|
|
Sinus Thrombosis, Intracranial [MESH:D012851] (356) |
|
|
Venous Thrombosis [MESH:D020246] (1141) |
|
|
Venous Thromboembolism [MESH:D054556] (400) |
|
|
|
|
|
Sinus Thrombosis, Intracranial [MESH:D012851] (356) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Myocardial Infarction [MESH:D009203] (4151) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Arteritis [MESH:D001167] (1084) |
|
 |
C15. Hemic and Lymphatic Diseases |
 |
 |
|
C15. Hemic and Lymphatic Diseases |
|
|
Anemia [MESH:D000740] (3966) |
|
|
Blood Platelet Disorders [MESH:D001791] (3174) |
|
|
Methemoglobinemia [MESH:D008708] (850) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Myelodysplastic Syndromes [MESH:D009190] (2093) |
|
|
Leukemia, Myelogenous, Chronic, BCR-ABL Positive [MESH:D015464] (1032) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Leukopenia [MESH:D007970] (1921) |
|
|
Disseminated Intravascular Coagulation [MESH:D004211] (462) |
|
|
Splenic Diseases [MESH:D013158] (1323) |
|
|
|
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
|
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
 |
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
 |
 |
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
|
|
|
Coffin-Siris syndrome [MESH:C536436] (102) |
|
|
Insulin-Like Growth Factor I, Resistance To [MESH:C564816] (141) |
|
|
Heart Defects, Congenital [MESH:D006330] (2611) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Coffin-Siris syndrome [MESH:C536436] (102) |
|
|
|
|
|
Coffin-Siris syndrome [MESH:C536436] (102) |
|
|
Neural Tube Defects [MESH:D009436] (2143) |
|
|
|
|
|
|
|
|
|
|
|
Coffin-Siris syndrome [MESH:C536436] (102) |
|
|
|
|
|
46, XX Disorders of Sex Development [MESH:D058489] (644) |
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
Fetal Growth Retardation [MESH:D005317] (986) |
|
|
|
|
|
Hypoprothrombinemias [MESH:D007020] (157) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
|
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
|
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
|
|
|
Lactate dehydrogenase deficiency type A [MESH:C538133] (119) |
|
|
Short chain Acyl CoA dehydrogenase deficiency [MESH:C537596] (38) |
|
|
Hyperlipidemia, Familial Combined [MESH:D006950] (372) |
|
|
Hyperlipoproteinemia Type I [MESH:D008072] (219) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
Hyperlipoproteinemia Type III [MESH:D006952] (181) |
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
|
|
|
|
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
Hemangioma, capillary infantile [MESH:C535860] (190) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
 |
C17. Skin and Connective Tissue Diseases |
 |
 |
|
C17. Skin and Connective Tissue Diseases |
|
|
|
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
Skin Diseases, Vascular [MESH:D017445] (3288) |
|
|
Skin Neoplasms [MESH:D012878] (2991) |
|
|
|
|
|
Breast Neoplasms, Male [MESH:D018567] (650) |
|
|
Drug Eruptions [MESH:D003875] (2697) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
|
|
|
Alopecia [MESH:D000505] (1453) |
|
|
|
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
Psoriasis [MESH:D011565] (3278) |
|
 |
C18. Nutritional and Metabolic Diseases |
 |
 |
|
C18. Nutritional and Metabolic Diseases |
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
Hepatic Encephalopathy [MESH:D006501] (1795) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
|
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
|
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Diabetes, Gestational [MESH:D016640] (1152) |
|
|
|
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
|
|
|
|
|
|
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) |
|
|
Hyperlipoproteinemia Type III [MESH:D006952] (181) |
|
|
Short chain Acyl CoA dehydrogenase deficiency [MESH:C537596] (38) |
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
|
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
|
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
|
|
|
Lactate dehydrogenase deficiency type A [MESH:C538133] (119) |
|
|
Short chain Acyl CoA dehydrogenase deficiency [MESH:C537596] (38) |
|
|
Hyperlipidemia, Familial Combined [MESH:D006950] (372) |
|
|
Hyperlipoproteinemia Type I [MESH:D008072] (219) |
|
|
Hyperlipoproteinemia Type II [MESH:D006938] (707) |
|
|
Hyperlipoproteinemia Type III [MESH:D006952] (181) |
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
|
|
|
|
|
|
Sea-Blue Histiocyte Syndrome [MESH:D012618] (165) |
|
|
Hepatolenticular Degeneration [MESH:D006527] (473) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
|
|
|
Cerebral Amyloid Angiopathy [MESH:D016657] (470) |
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
|
|
|
|
|
|
Porphyria Cutanea Tarda [MESH:D017119] (766) |
|
|
Hypokalemia [MESH:D007008] (1041) |
|
|
|
|
|
|
|
|
|
|
|
Vitamin A Deficiency [MESH:D014802] (705) |
|
|
Obesity [MESH:D009765] (4462) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
|
|
|
Diabetes, Gestational [MESH:D016640] (1152) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Ovarian Neoplasms [MESH:D010051] (3275) |
|
|
Pancreatic cancer, adult [MESH:C535836] (572) |
|
|
|
|
|
46, XX Disorders of Sex Development [MESH:D058489] (644) |
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
 |
C20. Immune System Diseases |
 |
 |
|
C20. Immune System Diseases |
|
|
|
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
|
|
|
|
|
|
Multiple Sclerosis, Relapsing-Remitting [MESH:D020529] (170) |
|
|
|
|
|
Drug Eruptions [MESH:D003875] (2695) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
|
|
|
Peanut Hypersensitivity [MESH:D021183] (572) |
|
|
Asthma [MESH:D001249] (3914) |
|
|
|
|
|
Acquired Immunodeficiency Syndrome [MESH:D000163] (743) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2767) |
|
|
Hodgkin Disease [MESH:D006689] (1082) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Schnitzler Syndrome [MESH:D019873] (110) |
|
 |
C22. Animal Diseases |
 |
 |
|
C22. Animal Diseases |
|
|
Mammary Neoplasms, Animal [MESH:D015674] (2735) |
|
|
Paratuberculosis [MESH:D010283] (427) |
|
 |
C23. Pathological Conditions, Signs and Symptoms |
 |
 |
|
C23. Pathological Conditions, Signs and Symptoms |
|
|
Alopecia [MESH:D000505] (1383) |
|
|
Atrophy [MESH:D001284] (2603) |
|
|
Plaque, Atherosclerotic [MESH:D058226] (696) |
|
|
|
|
|
Congenital diaphragmatic hernia [MESH:C538080] (381) |
|
|
Cardiomegaly [MESH:D006332] (3802) |
|
|
Hepatomegaly [MESH:D006529] (1169) |
|
|
Splenomegaly [MESH:D013163] (1258) |
|
|
Chromosome Aberrations [MESH:D002869] (2352) |
|
|
Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506) |
|
|
Fibrosis [MESH:D005355] (3133) |
|
|
Gliosis [MESH:D005911] (1419) |
|
|
Hemorrhage [MESH:D006470] (4451) |
|
|
Necrosis [MESH:D009336] (4019) |
|
|
Nerve Degeneration [MESH:D009410] (4061) |
|
|
Sclerosis [MESH:D012598] (224) |
|
|
Tachycardia [MESH:D013610] (3339) |
|
|
Disease Progression [MESH:D018450] (2868) |
|
|
Insulin-Like Growth Factor I, Resistance To [MESH:C564816] (141) |
|
|
Fetal Growth Retardation [MESH:D005317] (986) |
|
|
|
|
|
Sepsis [MESH:D018805] (3562) |
|
|
|
|
|
Malignant hyperthermia susceptibility type 1 [MESH:C535694] (51) |
|
|
Neoplasm Invasiveness [MESH:D009361] (3388) |
|
|
Neoplasm Metastasis [MESH:D009362] (4441) |
|
|
Neoplasm Recurrence, Local [MESH:D009364] (1949) |
|
|
Neoplasm, Residual [MESH:D018365] (478) |
|
|
Cell Transformation, Neoplastic [MESH:D002471] (3389) |
|
|
|
|
|
Malignant hyperthermia susceptibility type 1 [MESH:C535694] (51) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Asthenia [MESH:D001247] (376) |
|
|
Fever [MESH:D005334] (2856) |
|
|
Hypothermia [MESH:D007035] (2075) |
|
|
|
|
|
Weight Gain [MESH:D015430] (2595) |
|
|
Weight Loss [MESH:D015431] (2512) |
|
|
Obesity [MESH:D009765] (4454) |
|
|
Pain [MESH:D010146] (3869) |
|
|
Reflex, Abnormal [MESH:D012021] (485) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Ataxia [MESH:D001259] (984) |
|
|
Hyperkinesis [MESH:D006948] (1799) |
|
|
|
|
|
|
|
|
Language Development Disorders [MESH:D007805] (351) |
|
|
Speech Disorders [MESH:D013064] (482) |
|
|
Amnesia [MESH:D000647] (1911) |
|
|
Coffin-Siris syndrome [MESH:C536436] (102) |
|
|
|
|
|
Minicore Myopathy with External Ophthalmoplegia [MESH:C564969] (51) |
|
|
|
|
|
Hearing Loss [MESH:D034381] (2066) |
|
|
Hyperalgesia [MESH:D006930] (3929) |
|
|
|
|
|
|
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
|
Anorexia [MESH:D000855] (854) |
|
|
Diarrhea [MESH:D003967] (858) |
|
|
Hyperoxia [MESH:D018496] (694) |
|
|
Hyperventilation [MESH:D006985] (652) |
|
|
Respiratory Sounds [MESH:D012135] (713) |
|
|
Proteinuria [MESH:D011507] (3293) |
|
 |
C24. Occupational Diseases |
 |
 |
|
C24. Occupational Diseases |
|
|
Not Fully Specified [NFS] (1530) |
|
|
|
|
|
Silicosis [MESH:D012829] (1273) |
|
 |
C25. Chemically-Induced Disorders |
 |
 |
|
C25. Chemically-Induced Disorders |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Drug Eruptions [MESH:D003875] (2697) |
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Arsenic Poisoning [MESH:D020261] (2540) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Mercury Poisoning [MESH:D008630] (193) |
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Psychoses, Substance-Induced [MESH:D011605] (2053) |
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Amphetamine-Related Disorders [MESH:D019969] (2858) |
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Cocaine-Related Disorders [MESH:D019970] (3054) |
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Psychoses, Substance-Induced [MESH:D011605] (2052) |
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Substance Withdrawal Syndrome [MESH:D013375] (2956) |
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Alcoholism [MESH:D000437] (1519) |
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Heroin Dependence [MESH:D006556] (950) |
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Morphine Dependence [MESH:D009021] (855) |
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C26. Wounds and Injuries |
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C26. Wounds and Injuries |
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Extravasation of Diagnostic and Therapeutic Materials [MESH:D005119] (506) |
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Brain Injuries [MESH:D001930] (3431) |
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Radiation Injuries, Experimental [MESH:D011833] (2662) |
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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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Polychlorinated Biphenyls [MESH:D011078] (104) |
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Polychlorinated Biphenyls [MESH:D011078] (112) |
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F. Psychiatry and Psychology |
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F. Psychiatry and Psychology |
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Coffin-Siris syndrome [MESH:C536436] (102) |
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Alzheimer disease type 2 [MESH:C536595] (165) |
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Coffin-Siris syndrome [MESH:C536436] (102) |
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