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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CCAAT/enhancer binding protein (C/EBP), alpha [HGNC:CEBPA] (49) |
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cytochrome P450, family 01, subfamily A, polypeptide 01 [HGNC:CYP1A1] (566) |
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cytochrome P450, family 01, subfamily B, polypeptide 01 [HGNC:CYP1B1] (301) |
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adiponectin, C1Q and collagen domain containing [HGNC:ADIPOQ] (71) |
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fatty acid binding protein 4, adipocyte [HGNC:FABP4] (42) |
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heat shock 22kDa protein 08 [HGNC:HSPB8] (28) |
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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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peroxisome proliferator-activated receptor gamma [HGNC:PPARG] (234) |
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progesterone receptor [HGNC:PGR] (209) |
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fatty acid synthase [HGNC:FASN] (72) |
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UDP glucuronosyltransferase 2 family, polypeptide B15 [HGNC:UGT2B15] (85) |
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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 (2187) |
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reaction (3393) |
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activity (2865) |
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expression (3238) |
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reaction (1574) |
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4. Semantic Terms |
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4. Semantic Terms |
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Indicator, Reagent, or Diagnostic Aid [STY:T130] (903) |
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Pharmacologic Substance [STY:T121] (11019) |
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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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Peters anomaly [MESH:C537884] (465) |
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C04. Neoplasms |
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C04. Neoplasms |
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Hamartoma [MESH:D006222] (1484) |
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Neoplasms, Radiation-Induced [MESH:D009381] (174) |
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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, Promyelocytic, Acute [MESH:D015473] (1367) |
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Lymphoma, T-Cell [MESH:D016399] (1405) |
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Liposarcoma [MESH:D008080] (612) |
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Leiomyoma [MESH:D007889] (744) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Liposarcoma [MESH:D008080] (612) |
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Medulloblastoma [MESH:D008527] (1282) |
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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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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Carcinoma, Transitional Cell [MESH:D002295] (2662) |
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Carcinoma, Adenoid Cystic [MESH:D003528] (1561) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Thyroid cancer, follicular [MESH:C572845] (674) |
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Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565) |
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Mesothelioma [MESH:D008654] (2567) |
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Medulloblastoma [MESH:D008527] (1282) |
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Medulloblastoma [MESH:D008527] (1282) |
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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Papilloma [MESH:D010212] (2243) |
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Meningioma [MESH:D008579] (978) |
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Medulloblastoma [MESH:D008527] (1282) |
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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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Hemangiosarcoma [MESH:D006394] (1836) |
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Meningioma [MESH:D008579] (978) |
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Melanoma [MESH:D008545] (3508) |
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Skin Neoplasms [MESH:D012878] (2992) |
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Breast Neoplasms, Male [MESH:D018567] (650) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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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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Esophageal Neoplasms [MESH:D004938] (3737) |
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Thyroid Neoplasms [MESH:D013964] (2040) |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Brain Neoplasms [MESH:D001932] (2764) |
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Meningioma [MESH:D008579] (978) |
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Lung Neoplasms [MESH:D008175] (6015) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Kidney Neoplasms [MESH:D007680] (3966) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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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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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Bone Diseases, Metabolic [MESH:D001851] (3492) |
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Arthritis, Experimental [MESH:D001169] (3142) |
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Arthritis, Rheumatoid [MESH:D001172] (3603) |
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Osteoarthritis [MESH:D010003] (1743) |
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Myoglobinuria, Acute Recurrent, Autosomal Recessive [MESH:C564832] (64) |
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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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Barrett Esophagus [MESH:D001471] (1930) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Barrett Esophagus [MESH:D001471] (1930) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Crohn Disease [MESH:D003424] (2585) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Cecal Neoplasms [MESH:D002430] (822) |
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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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Colorectal Neoplasms [MESH:D015179] (4534) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Stomach Ulcer [MESH:D013276] (2915) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567) |
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Hepatitis, Autoimmune [MESH:D019693] (1982) |
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Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Oral Ulcer [MESH:D019226] (488) |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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C08. Respiratory Tract Diseases |
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C08. Respiratory Tract Diseases |
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Lung Neoplasms [MESH:D008175] (6012) |
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Pulmonary Disease, Chronic Obstructive [MESH:D029424] (3564) |
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Acute Lung Injury [MESH:D055371] (1907) |
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Lung Neoplasms [MESH:D008175] (6013) |
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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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Brain Neoplasms [MESH:D001932] (2764) |
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Sandhoff Disease [MESH:D012497] (73) |
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Sandhoff Disease [MESH:D012497] (73) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Seizures [MESH:D012640] (4502) |
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Migraine Disorders [MESH:D008881] (2318) |
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Pituitary ACTH Hypersecretion [MESH:D047748] (599) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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Brain Neoplasms [MESH:D001932] (2764) |
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Meningioma [MESH:D008579] (978) |
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von Hippel-Lindau Disease [MESH:D006623] (580) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Seizures [MESH:D012640] (4514) |
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Peripheral Nervous System Diseases [MESH:D010523] (6151) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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C11. Eye Diseases |
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C11. Eye Diseases |
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Peters anomaly [MESH:C537884] (465) |
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Peters anomaly [MESH:C537884] (465) |
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Glaucoma 3, Primary Congenital, A [MESH:C565547] (434) |
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Glaucoma, Primary Open Angle [MESH:C562750] (466) |
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Glaucoma 1, Open Angle, A [MESH:C564234] (446) |
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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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Oligospermia [MESH:D009845] (799) |
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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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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Hypospadias 1, X-Linked [MESH:C567482] (571) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Kidney Neoplasms [MESH:D007680] (3966) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Kidney Neoplasms [MESH:D007680] (3966) |
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Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522) |
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Glomerulonephritis [MESH:D005921] (3758) |
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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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Not Fully Specified [NFS] (1116) |
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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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46, XX Disorders of Sex Development [MESH:D058489] (644) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Hypospadias 1, X-Linked [MESH:C567482] (571) |
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Ovarian Neoplasms [MESH:D010051] (3281) |
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Kidney Neoplasms [MESH:D007680] (3966) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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|
Kidney Neoplasms [MESH:D007680] (3966) |
|
|
|
|
|
Polycystic Kidney, Autosomal Dominant [MESH:D016891] (522) |
|
|
Glomerulonephritis [MESH:D005921] (3758) |
|
|
Acute Kidney Injury [MESH:D058186] (4142) |
|
|
Kidney Failure, Chronic [MESH:D007676] (2930) |
|
|
Urinary Bladder Neoplasms [MESH:D001749] (4079) |
|
|
Abortion, Spontaneous [MESH:D000022] (2780) |
|
|
Diabetes, Gestational [MESH:D016640] (1157) |
|
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C14. Cardiovascular Diseases |
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|
C14. Cardiovascular Diseases |
|
|
|
|
|
Cardiomegaly [MESH:D006332] (4081) |
|
|
Heart Failure [MESH:D006333] (4058) |
|
|
Tachycardia [MESH:D013610] (3339) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Myocardial Infarction [MESH:D009203] (4122) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Arteritis [MESH:D001167] (1084) |
|
|
Hyperemia [MESH:D006940] (2372) |
|
|
Hypertension [MESH:D006973] (5655) |
|
|
Peripheral Vascular Diseases [MESH:D016491] (1412) |
|
|
von Hippel-Lindau Disease [MESH:D006623] (580) |
|
|
|
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Carotid Intimal Medial Thickness 1 [MESH:C563733] (457) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Myocardial Infarction [MESH:D009203] (4151) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Coronary Artery Disease [MESH:D003324] (2685) |
|
|
Coronary Restenosis [MESH:D023903] (1683) |
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Arteritis [MESH:D001167] (1084) |
|
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C15. Hemic and Lymphatic Diseases |
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|
C15. Hemic and Lymphatic Diseases |
|
|
|
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
|
Leukostasis [MESH:D018921] (769) |
|
|
|
|
|
|
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
|
|
|
Lymphoma, T-Cell [MESH:D016399] (1204) |
|
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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
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|
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
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|
|
|
|
|
|
|
Peters anomaly [MESH:C537884] (465) |
|
|
|
|
|
46, XX Disorders of Sex Development [MESH:D058489] (644) |
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Hypospadias 1, X-Linked [MESH:C567482] (571) |
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Sandhoff Disease [MESH:D012497] (73) |
|
|
Sandhoff Disease [MESH:D012497] (73) |
|
|
|
|
|
|
|
|
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|
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|
|
Sandhoff Disease [MESH:D012497] (73) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Sandhoff Disease [MESH:D012497] (73) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
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C17. Skin and Connective Tissue Diseases |
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|
C17. Skin and Connective Tissue Diseases |
|
|
|
|
|
Arthritis, Rheumatoid [MESH:D001172] (3603) |
|
|
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) |
|
|
|
|
|
Lipodystrophy, Familial Partial [MESH:D052496] (589) |
|
|
Psoriasis [MESH:D011565] (3278) |
|
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C18. Nutritional and Metabolic Diseases |
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|
C18. Nutritional and Metabolic Diseases |
|
|
Not Fully Specified [NFS] (817) |
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Sandhoff Disease [MESH:D012497] (73) |
|
|
Sandhoff Disease [MESH:D012497] (73) |
|
|
|
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Diabetes, Gestational [MESH:D016640] (1152) |
|
|
|
|
|
Metabolic Syndrome X [MESH:D024821] (2151) |
|
|
Dyslipidemias [MESH:D050171] (2428) |
|
|
Lipodystrophy, Familial Partial [MESH:D052496] (589) |
|
|
|
|
|
|
|
|
|
|
|
Sandhoff Disease [MESH:D012497] (73) |
|
|
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|
|
|
|
|
|
|
|
|
|
|
Sandhoff Disease [MESH:D012497] (73) |
|
|
Sandhoff Disease [MESH:D012497] (73) |
|
|
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|
|
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|
|
|
|
|
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|
|
Sandhoff Disease [MESH:D012497] (73) |
|
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|
|
|
|
|
|
|
Sandhoff Disease [MESH:D012497] (73) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
|
|
|
Lipodystrophy, Familial Partial [MESH:D052496] (589) |
|
|
Hypokalemia [MESH:D007008] (1041) |
|
|
|
|
|
|
|
|
Obesity, Morbid [MESH:D009767] (515) |
|
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C19. Endocrine System Diseases |
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|
C19. Endocrine System Diseases |
|
|
|
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Diabetes, Gestational [MESH:D016640] (1152) |
|
|
Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
|
|
Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
|
|
Ovarian Neoplasms [MESH:D010051] (3275) |
|
|
Pancreatic Neoplasms [MESH:D010190] (3820) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
|
Hypogonadism [MESH:D007006] (1123) |
|
|
46, XX Disorders of Sex Development [MESH:D058489] (644) |
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
|
Ovarian Neoplasms [MESH:D010051] (3281) |
|
|
Polycystic Ovary Syndrome [MESH:D011085] (2186) |
|
|
Hyperparathyroidism [MESH:D006961] (1475) |
|
|
|
|
|
Pituitary ACTH Hypersecretion [MESH:D047748] (599) |
|
|
Thyroid Neoplasms [MESH:D013964] (2040) |
|
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C20. Immune System Diseases |
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|
C20. Immune System Diseases |
|
|
|
|
|
Arthritis, Rheumatoid [MESH:D001172] (3601) |
|
|
Hepatitis, Autoimmune [MESH:D019693] (1982) |
|
|
|
|
|
Drug Eruptions [MESH:D003875] (2695) |
|
|
Dermatitis, Allergic Contact [MESH:D017449] (3241) |
|
|
|
|
|
Multiple Myeloma [MESH:D009101] (2767) |
|
|
|
|
|
Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
|
|
|
|
|
Lymphoma, T-Cell [MESH:D016399] (1382) |
|
|
Multiple Myeloma [MESH:D009101] (2765) |
|
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C22. Animal Diseases |
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|
C22. Animal Diseases |
|
|
Disease Models, Animal [MESH:D004195] (2058) |
|
|
Mammary Neoplasms, Animal [MESH:D015674] (2735) |
|
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C23. Pathological Conditions, Signs and Symptoms |
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|
C23. Pathological Conditions, Signs and Symptoms |
|
|
Alopecia [MESH:D000505] (1383) |
|
|
Cardiomegaly [MESH:D006332] (3802) |
|
|
Intestinal Polyps [MESH:D007417] (1592) |
|
|
Hyperplasia [MESH:D006965] (2463) |
|
|
Inflammation [MESH:D007249] (5241) |
|
|
Ischemia [MESH:D007511] (3049) |
|
|
Lithiasis [MESH:D020347] (345) |
|
|
Nerve Degeneration [MESH:D009410] (4061) |
|
|
Tachycardia [MESH:D013610] (3339) |
|
|
Disease Progression [MESH:D018450] (2868) |
|
|
Recurrence [MESH:D012008] (830) |
|
|
Neoplasm Metastasis [MESH:D009362] (4441) |
|
|
Neoplasm Recurrence, Local [MESH:D009364] (1949) |
|
|
Cell Transformation, Neoplastic [MESH:D002471] (3389) |
|
|
|
|
|
Myocardial Reperfusion Injury [MESH:D015428] (3500) |
|
|
Feminization [MESH:D005262] (655) |
|
|
|
|
|
Weight Gain [MESH:D015430] (2595) |
|
|
Weight Loss [MESH:D015431] (2512) |
|
|
|
|
|
Obesity, Morbid [MESH:D009767] (515) |
|
|
Seizures [MESH:D012640] (4502) |
|
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C24. Occupational Diseases |
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|
C24. Occupational Diseases |
|
|
Occupational Diseases [MESH:D009784] (3402) |
|
|
Not Fully Specified [NFS] (1530) |
|
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C25. Chemically-Induced Disorders |
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|
C25. Chemically-Induced Disorders |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Drug Eruptions [MESH:D003875] (2697) |
|
|
Drug-Induced Liver Injury [MESH:D056486] (4936) |
|
|
Psychoses, Substance-Induced [MESH:D011605] (2053) |
|
|
Cocaine-Related Disorders [MESH:D019970] (3054) |
|
|
Psychoses, Substance-Induced [MESH:D011605] (2052) |
|
|
Heroin Dependence [MESH:D006556] (950) |
|
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C26. Wounds and Injuries |
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|
C26. Wounds and Injuries |
|
|
|
|
|
Neoplasms, Radiation-Induced [MESH:D009381] (171) |
|
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D02. Organic Chemicals |
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|
D02. Organic Chemicals |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Parabens [MESH:D010226] (36) |
|
|
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|
|
Parabens [MESH:D010226] (36) |
|
|
|
|
|
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|
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|
|
Parabens [MESH:D010226] (36) |
|
|
|
|
|
Parabens [MESH:D010226] (36) |
|
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
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E. Analytical, Diagnostic and Therapeutic Techniques and Equipment |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Carotid Intimal Medial Thickness 1 [MESH:C563733] (457) |
|
|
|
|
|
Carotid Intimal Medial Thickness 1 [MESH:C563733] (457) |
|
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F. Psychiatry and Psychology |
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|
F. Psychiatry and Psychology |
|
|
|
|
|
|
|
|
|
|
|
Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
|
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G. Phenomena and Processes |
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|
G. Phenomena and Processes |
|
|
|
|
|
|
|
|
Carotid Intimal Medial Thickness 1 [MESH:C563733] (457) |
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