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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cytochrome P450, family 02, subfamily E, polypeptide 01 [HGNC:CYP2E1] (225) |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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metabolic processing (740) |
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4. Semantic Terms |
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4. Semantic Terms |
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Pharmacologic Substance [STY:T121] (11019) |
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Organic Chemical [STY:T109] (44144) |
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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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Atypical Mycobacteriosis, Familial, X-Linked 1 [MESH:C567070] (56) |
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Invasive Pneumococcal Disease, Recurrent Isolated, 2 [MESH:C564468] (56) |
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Majeed syndrome [MESH:C537839] (33) |
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Endotoxemia [MESH:D019446] (1289) |
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Endotoxemia [MESH:D019446] (1289) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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Hepatitis B, Chronic [MESH:D019694] (277) |
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Hepatitis B, Chronic [MESH:D019694] (277) |
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Influenza, Human [MESH:D007251] (1075) |
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HIV Infections [MESH:D015658] (3402) |
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HIV Infections [MESH:D015658] (3296) |
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C03. Parasitic Diseases |
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C03. Parasitic Diseases |
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Malaria [MESH:D008288] (2175) |
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C04. Neoplasms |
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C04. Neoplasms |
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Precancerous Conditions [MESH:D011230] (2858) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Leukemia, Monocytic, Acute [MESH:D007948] (98) |
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Lymphangioleiomyomatosis [MESH:D018192] (162) |
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Lymphoma, Non-Hodgkin [MESH:D008228] (3337) |
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Mastocytosis, Systemic [MESH:D034721] (769) |
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Osteosarcoma [MESH:D012516] (2175) |
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Lymphangioleiomyomatosis [MESH:D018192] (162) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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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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Mesothelioma [MESH:D008654] (2567) |
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Carcinoma, Lewis Lung [MESH:D018827] (248) |
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Carcinoma, Transitional Cell [MESH:D002295] (2662) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Carcinoma, Adenoid Cystic [MESH:D003528] (1561) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Cholangiocarcinoma [MESH:D018281] (2398) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Mesothelioma [MESH:D008654] (2567) |
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Glioblastoma [MESH:D005909] (2554) |
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Papilloma [MESH:D010212] (2243) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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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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Hemangiosarcoma [MESH:D006394] (1836) |
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Melanoma [MESH:D008545] (3508) |
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Breast Neoplasms [MESH:D001943] (6077) |
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Bile Duct Neoplasms [MESH:D001650] (367) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Rectal Neoplasms [MESH:D012004] (717) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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Tongue Neoplasms [MESH:D014062] (1518) |
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Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Brain Neoplasms [MESH:D001932] (2764) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Small Cell Lung Carcinoma [MESH:D055752] (1380) |
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Uterine Cervical Neoplasms [MESH:D002583] (978) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Carcinoma, Lewis Lung [MESH:D018827] (248) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Recurrence, Local [MESH:D009364] (1949) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Lymphatic Metastasis [MESH:D008207] (917) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Osteitis Deformans [MESH:D010001] (287) |
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Fibrous Dysplasia of Bone [MESH:D005357] (737) |
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Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56) |
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Majeed syndrome [MESH:C537839] (33) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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Osteoarthritis [MESH:D010003] (1743) |
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Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
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Amish lethal microcephaly [MESH:C538247] (29) |
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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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Bile Duct Neoplasms [MESH:D001650] (367) |
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Bile Duct Neoplasms [MESH:D001650] (367) |
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Gallstones [MESH:D042882] (350) |
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Gallstones [MESH:D042882] (350) |
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Bile Duct Neoplasms [MESH:D001650] (367) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Rectal Neoplasms [MESH:D012004] (717) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Liver Neoplasms, Experimental [MESH:D008114] (2837) |
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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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Esophageal Squamous Cell Carcinoma [MESH:C562729] (2396) |
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Colitis [MESH:D003092] (3199) |
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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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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Rectal Neoplasms [MESH:D012004] (717) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colitis [MESH:D003092] (3199) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Crohn Disease [MESH:D003424] (2585) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Rectal Neoplasms [MESH:D012004] (717) |
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Rectal Neoplasms [MESH:D012004] (717) |
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Gastroparesis [MESH:D018589] (732) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Hepatorenal Syndrome [MESH:D006530] (910) |
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Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567) |
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Hepatitis B, Chronic [MESH:D019694] (277) |
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Hepatitis B, Chronic [MESH:D019694] (277) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
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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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Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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Tongue Neoplasms [MESH:D014062] (1518) |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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Tongue Neoplasms [MESH:D014062] (1518) |
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Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
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Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
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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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Lung Injury [MESH:D055370] (3688) |
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Pneumonia [MESH:D011014] (3482) |
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Pulmonary Fibrosis [MESH:D011658] (3140) |
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Asthma [MESH:D001249] (3903) |
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Pulmonary Emphysema [MESH:D011656] (1259) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Small Cell Lung Carcinoma [MESH:D055752] (1380) |
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Asthma [MESH:D001249] (4098) |
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Influenza, Human [MESH:D007251] (1075) |
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Pneumonia [MESH:D011014] (3482) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Small Cell Lung Carcinoma [MESH:D055752] (1380) |
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C09. Otorhinolaryngologic Diseases |
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C09. Otorhinolaryngologic Diseases |
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Deafness, Autosomal Dominant 5 [MESH:C563410] (30) |
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Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
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Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
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Nasopharyngeal Neoplasms [MESH:D009303] (1500) |
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C10. Nervous System Diseases |
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C10. Nervous System Diseases |
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Not Fully Specified [NFS] (4027) |
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Brain Injuries [MESH:D001930] (3429) |
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Brain Neoplasms [MESH:D001932] (2764) |
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Huntington Disease [MESH:D006816] (540) |
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Parkinson Disease [MESH:D010300] (3595) |
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Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Carotid Artery Diseases [MESH:D002340] (1993) |
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Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
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Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
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Cerebral Hemorrhage [MESH:D002543] (2873) |
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Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Huntington Disease [MESH:D006816] (540) |
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Seizures [MESH:D012640] (4502) |
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Status Epilepticus [MESH:D013226] (4014) |
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Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Huntington Disease [MESH:D006816] (540) |
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Parkinson Disease [MESH:D010300] (3595) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219) |
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Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219) |
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Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178) |
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Amish lethal microcephaly [MESH:C538247] (29) |
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Brain Neoplasms [MESH:D001932] (2764) |
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von Hippel-Lindau Disease [MESH:D006623] (580) |
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Parkinson Disease [MESH:D010300] (3595) |
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Huntington Disease [MESH:D006816] (540) |
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Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178) |
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Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219) |
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Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178) |
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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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Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Seizures [MESH:D012640] (4514) |
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Hyperkinesis [MESH:D006948] (1799) |
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Learning Disorders [MESH:D007859] (2727) |
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Down Syndrome [MESH:D004314] (1287) |
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Williams Syndrome [MESH:D018980] (133) |
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Adrenoleukodystrophy [MESH:D000326] (1348) |
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Deafness, Autosomal Dominant 5 [MESH:C563410] (30) |
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Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
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Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219) |
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Neuronopathy, Distal Hereditary Motor, Type IIB [MESH:C567084] (219) |
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Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
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Diabetic Neuropathies [MESH:D003929] (2442) |
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Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219) |
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Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178) |
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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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Retinitis Pigmentosa 31 [MESH:C563685] (14) |
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Retinitis Pigmentosa 31 [MESH:C563685] (14) |
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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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Prostatic Neoplasms [MESH:D011471] (6135) |
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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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Hepatorenal Syndrome [MESH:D006530] (910) |
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Uremia [MESH:D014511] (2898) |
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Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
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Glomerulopathy with fibronectin deposits [MESH:C536826] (244) |
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Acute Kidney Injury [MESH:D058186] (4142) |
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Kidney Failure, Chronic [MESH:D007676] (2930) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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C13. Female Urogenital Diseases and Pregnancy Complications |
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C13. Female Urogenital Diseases and Pregnancy Complications |
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Endometriosis [MESH:D004715] (2461) |
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Ovarian Neoplasms [MESH:D010051] (3281) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Infertility, Female [MESH:D007247] (2184) |
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Uterine Cervical Neoplasms [MESH:D002583] (978) |
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Uterine Cervical Neoplasms [MESH:D002583] (978) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Uterine Cervical Neoplasms [MESH:D002583] (978) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Hepatorenal Syndrome [MESH:D006530] (910) |
|
|
Uremia [MESH:D014511] (2898) |
|
|
|
|
|
Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462) |
|
|
Carcinoma, Renal Cell [MESH:D002292] (2975) |
|
|
|
|
|
Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
|
|
Glomerulopathy with fibronectin deposits [MESH:C536826] (244) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Pre-Eclampsia [MESH:D011225] (1435) |
|
|
Prenatal Exposure Delayed Effects [MESH:D011297] (870) |
|
 |
C14. Cardiovascular Diseases |
 |
 |
|
C14. Cardiovascular Diseases |
|
|
|
|
|
|
|
|
Coronary Vessel Anomalies [MESH:D003330] (317) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
|
|
Cardiomyopathy, Dilated [MESH:D002311] (1576) |
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1516) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Coronary Vessel Anomalies [MESH:D003330] (317) |
|
|
Aortic Valve Insufficiency [MESH:D001022] (1002) |
|
|
|
|
|
Cardiomyopathy, Hypertrophic [MESH:D002312] (1451) |
|
|
Williams Syndrome [MESH:D018980] (133) |
|
|
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) |
|
|
Diabetic Angiopathies [MESH:D003925] (1984) |
|
|
Hypertension [MESH:D006973] (5655) |
|
|
Vascular System Injuries [MESH:D057772] (2086) |
|
|
von Hippel-Lindau Disease [MESH:D006623] (580) |
|
|
|
|
|
Atherosclerosis [MESH:D050197] (4188) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Carotid Artery Diseases [MESH:D002340] (1993) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Cerebral Hemorrhage [MESH:D002543] (2873) |
|
|
|
|
|
|
|
|
Infarction, Middle Cerebral Artery [MESH:D020244] (2268) |
|
|
Thrombosis [MESH:D013927] (3101) |
|
|
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) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
 |
C15. Hemic and Lymphatic Diseases |
 |
 |
|
C15. Hemic and Lymphatic Diseases |
|
|
Blood Coagulation Disorders [MESH:D001778] (1828) |
|
|
Thrombophilia [MESH:D019851] (592) |
|
|
Anemia, Sideroblastic [MESH:D000756] (636) |
|
|
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to [MESH:C565557] (312) |
|
|
Anemia, Hemolytic, Autoimmune [MESH:D000744] (117) |
|
|
|
|
|
Majeed syndrome [MESH:C537839] (33) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
Anemia, Sideroblastic [MESH:D000756] (636) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56) |
|
|
|
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Lymphangioleiomyomatosis [MESH:D018192] (162) |
|
|
Lymphoma, Non-Hodgkin [MESH:D008228] (3330) |
|
 |
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
 |
 |
|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
|
|
|
|
|
|
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Incontinentia Pigmenti [MESH:D007184] (57) |
|
|
Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56) |
|
|
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56) |
|
|
|
|
|
Coronary Vessel Anomalies [MESH:D003330] (317) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Williams Syndrome [MESH:D018980] (133) |
|
|
|
|
|
|
|
|
Amish lethal microcephaly [MESH:C538247] (29) |
|
|
|
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219) |
|
|
Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178) |
|
|
|
|
|
Amish lethal microcephaly [MESH:C538247] (29) |
|
|
Incontinentia Pigmenti [MESH:D007184] (57) |
|
|
Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56) |
|
|
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56) |
|
|
Polycystic Kidney, Autosomal Recessive [MESH:D017044] (462) |
|
|
|
|
|
Majeed syndrome [MESH:C537839] (33) |
|
|
Down Syndrome [MESH:D004314] (1287) |
|
|
Williams Syndrome [MESH:D018980] (133) |
|
|
|
|
|
Retinitis Pigmentosa 31 [MESH:C563685] (14) |
|
|
Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56) |
|
|
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56) |
|
|
Atypical Mycobacteriosis, Familial, X-Linked 1 [MESH:C567070] (56) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Huntington Disease [MESH:D006816] (540) |
|
|
Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178) |
|
|
|
|
|
Charcot-Marie-Tooth disease, Type 2F [MESH:C535413] (219) |
|
|
Spastic paraplegia 13, autosomal dominant [MESH:C537485] (178) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2565) |
|
|
|
|
|
Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Muscular Dystrophy, Facioscapulohumeral [MESH:D020391] (854) |
|
|
Incontinentia Pigmenti [MESH:D007184] (57) |
|
|
Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56) |
|
|
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56) |
|
 |
C17. Skin and Connective Tissue Diseases |
 |
 |
|
C17. Skin and Connective Tissue Diseases |
|
|
|
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
|
|
|
Chloracne [MESH:D054506] (1274) |
|
|
Breast Neoplasms [MESH:D001943] (6077) |
|
|
Drug Eruptions [MESH:D003875] (2697) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
|
|
|
Chloracne [MESH:D054506] (1274) |
|
|
Incontinentia Pigmenti [MESH:D007184] (57) |
|
|
Incontinentia Pigmenti [MESH:D007184] (57) |
|
|
Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56) |
|
|
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56) |
|
|
|
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
Incontinentia Pigmenti [MESH:D007184] (57) |
|
|
Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56) |
|
|
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56) |
|
 |
C18. Nutritional and Metabolic Diseases |
 |
 |
|
C18. Nutritional and Metabolic Diseases |
|
|
Iron Metabolism Disorders [MESH:D019189] (2139) |
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
|
|
|
|
|
|
Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Glucose Intolerance [MESH:D018149] (605) |
|
|
|
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
|
|
|
|
|
|
Hypercholesterolemia [MESH:D006937] (1404) |
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Amino Acid Metabolism, Inborn Errors [MESH:D000592] (2559) |
|
|
|
|
|
Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
|
|
|
|
|
|
Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Leukodystrophy, Hypomyelinating, 4 [MESH:C567390] (178) |
|
|
|
|
|
|
|
|
Amyotrophic lateral sclerosis 1 [MESH:C531617] (2559) |
|
|
|
|
|
Obesity [MESH:D009765] (4462) |
|
 |
C19. Endocrine System Diseases |
 |
 |
|
C19. Endocrine System Diseases |
|
|
|
|
|
|
|
|
Adrenoleukodystrophy [MESH:D000326] (1348) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Diabetic Angiopathies [MESH:D003925] (1984) |
|
|
Diabetic Neuropathies [MESH:D003929] (2443) |
|
|
Ovarian Neoplasms [MESH:D010051] (3275) |
|
|
Carcinoma, Pancreatic Ductal [MESH:D021441] (1056) |
|
|
|
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
Hyperparathyroidism [MESH:D006961] (1475) |
|
 |
C20. Immune System Diseases |
 |
 |
|
C20. Immune System Diseases |
|
|
|
|
|
Anemia, Hemolytic, Autoimmune [MESH:D000744] (117) |
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Glomerulopathy with fibronectin deposits [MESH:C536826] (244) |
|
|
|
|
|
Drug Eruptions [MESH:D003875] (2695) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
|
|
|
Asthma [MESH:D001249] (3914) |
|
|
Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56) |
|
|
Immunodeficiency without anhidrotic ectodermal dysplasia [MESH:C536289] (56) |
|
|
Invasive Pneumococcal Disease, Recurrent Isolated, 2 [MESH:C564468] (56) |
|
|
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56) |
|
|
HIV Infections [MESH:D015658] (3402) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2767) |
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
Lymphangioleiomyomatosis [MESH:D018192] (162) |
|
|
Lymphoma, Non-Hodgkin [MESH:D008228] (3330) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
 |
C22. Animal Diseases |
 |
 |
|
C22. Animal Diseases |
|
|
Mammary Neoplasms, Animal [MESH:D015674] (2735) |
|
 |
C23. Pathological Conditions, Signs and Symptoms |
 |
 |
|
C23. Pathological Conditions, Signs and Symptoms |
|
|
|
|
|
Gallstones [MESH:D042882] (350) |
|
|
|
|
|
Congenital diaphragmatic hernia [MESH:C538080] (381) |
|
|
|
|
|
Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
|
|
Intestinal Polyps [MESH:D007417] (1592) |
|
|
Fibrosis [MESH:D005355] (3133) |
|
|
Growth Disorders [MESH:D006130] (2438) |
|
|
Hyperplasia [MESH:D006965] (2463) |
|
|
Ischemia [MESH:D007511] (3049) |
|
|
Necrosis [MESH:D009336] (4019) |
|
|
Micronuclei, Chromosome-Defective [MESH:D048629] (1013) |
|
|
Disease Progression [MESH:D018450] (2868) |
|
|
|
|
|
Cerebral Hemorrhage [MESH:D002543] (2872) |
|
|
|
|
|
|
|
|
|
|
|
Endotoxemia [MESH:D019446] (1289) |
|
|
Neoplasm Invasiveness [MESH:D009361] (3388) |
|
|
Neoplasm Recurrence, Local [MESH:D009364] (1949) |
|
|
Cell Transformation, Neoplastic [MESH:D002471] (3389) |
|
|
Lymphatic Metastasis [MESH:D008207] (917) |
|
|
|
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
|
|
|
|
|
|
Weight Gain [MESH:D015430] (2595) |
|
|
Obesity [MESH:D009765] (4454) |
|
|
Seizures [MESH:D012640] (4502) |
|
|
Hyperkinesis [MESH:D006948] (1799) |
|
|
|
|
|
Learning Disorders [MESH:D007859] (2727) |
|
|
Gastroparesis [MESH:D018589] (732) |
|
|
|
|
|
|
|
|
|
|
|
Deafness, Autosomal Dominant 5 [MESH:C563410] (30) |
|
|
|
|
|
|
|
|
Acute Coronary Syndrome [MESH:D054058] (2286) |
|
 |
C25. Chemically-Induced Disorders |
 |
 |
|
C25. Chemically-Induced Disorders |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Drug Eruptions [MESH:D003875] (2697) |
|
|
Arsenic Poisoning [MESH:D020261] (2540) |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Neurotoxicity Syndromes [MESH:D020258] (3323) |
|
|
Amphetamine-Related Disorders [MESH:D019969] (2858) |
|
|
Cocaine-Related Disorders [MESH:D019970] (3054) |
|
|
Substance Withdrawal Syndrome [MESH:D013375] (2956) |
|
|
Alcoholism [MESH:D000437] (1519) |
|
|
|
|
|
Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
|
 |
C26. Wounds and Injuries |
 |
 |
|
C26. Wounds and Injuries |
|
|
Not Fully Specified [NFS] (2454) |
|
|
Vascular System Injuries [MESH:D057772] (2086) |
|
|
Brain Injuries [MESH:D001930] (3431) |
|
|
Lung Injury [MESH:D055370] (1814) |
|
|
|
|
|
Brain Injuries [MESH:D001930] (3431) |
|
 |
D02. Organic Chemicals |
 |
 |
|
D02. Organic Chemicals |
|
|
|
|
|
Formamides [MESH:D005559] (59) |
|
|
|
|
|
|
|
|
Formamides [MESH:D005559] (59) |
|
 |