more general categories |
information about this item |
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1. Human Genes |
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1. Human Genes |
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ATP-binding cassette, sub-family G (WHITE), member 1 [HGNC:ABCG1] (40) |
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collagen, type I, alpha 1 [HGNC:COL1A1] (123) |
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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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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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cotreatment (1499) |
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expression (2187) |
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reaction (3393) |
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expression (3238) |
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phosphorylation (1060) |
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reaction (1574) |
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secretion (901) |
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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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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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HIV Infections [MESH:D015658] (3402) |
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HIV Infections [MESH:D015658] (3296) |
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C04. Neoplasms |
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C04. Neoplasms |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Breast Neoplasms [MESH:D001943] (6077) |
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Head and Neck Neoplasms [MESH:D006258] (4612) |
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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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Ovarian Neoplasms [MESH:D010051] (3275) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Kidney Neoplasms [MESH:D007680] (3966) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Metastasis [MESH:D009362] (4441) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Hyperostosis, Cortical, Congenital [MESH:D006958] (392) |
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Osteogenesis imperfecta, type 2A [MESH:C536042] (375) |
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Osteogenesis imperfecta, type 3 [MESH:C536044] (375) |
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Osteogenesis imperfecta, type 4 [MESH:C536045] (375) |
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Osteoporosis [MESH:D010024] (3037) |
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Hyperostosis, Cortical, Congenital [MESH:D006958] (392) |
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Arthritis, Experimental [MESH:D001169] (3142) |
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C06. Digestive System Diseases |
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C06. Digestive System Diseases |
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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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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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Crohn Disease [MESH:D003424] (2585) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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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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Fatty Liver [MESH:D005234] (3584) |
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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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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Behcet Syndrome [MESH:D001528] (1784) |
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Oral Submucous Fibrosis [MESH:D009914] (2432) |
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Oral Ulcer [MESH:D019226] (488) |
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C08. Respiratory Tract Diseases |
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C08. Respiratory Tract Diseases |
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Acute Lung Injury [MESH:D055371] (1907) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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Adenocarcinoma of lung [MESH:C538231] (1487) |
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C09. Otorhinolaryngologic Diseases |
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C09. Otorhinolaryngologic Diseases |
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Auditory Perceptual Disorders [MESH:D001308] (82) |
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C10. Nervous System Diseases |
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C10. Nervous System Diseases |
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Auditory Perceptual Disorders [MESH:D001308] (82) |
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Brain Ischemia [MESH:D002545] (4873) |
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Stroke [MESH:D020521] (3702) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Epilepsy, Generalized [MESH:D004829] (1431) |
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Seizures [MESH:D012640] (4502) |
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Spina Bifida Cystica [MESH:D016137] (209) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Seizures [MESH:D012640] (4514) |
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Ataxia with vitamin E deficiency [MESH:C535393] (271) |
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Memory Disorders [MESH:D008569] (3233) |
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Learning Disorders [MESH:D007859] (2727) |
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Auditory Perceptual Disorders [MESH:D001308] (82) |
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Hyperalgesia [MESH:D006930] (3929) |
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Tangier Disease [MESH:D013631] (170) |
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C11. Eye Diseases |
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C11. Eye Diseases |
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Behcet Syndrome [MESH:D001528] (1784) |
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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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Kidney Neoplasms [MESH:D007680] (3966) |
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Kidney Neoplasms [MESH:D007680] (3966) |
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Glomerulonephritis, Membranous [MESH:D015433] (642) |
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Nephrotic Syndrome [MESH:D009404] (1536) |
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Kidney Failure, Chronic [MESH:D007676] (2930) |
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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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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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Ovarian Neoplasms [MESH:D010051] (3281) |
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Kidney Neoplasms [MESH:D007680] (3966) |
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Kidney Neoplasms [MESH:D007680] (3966) |
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Glomerulonephritis, Membranous [MESH:D015433] (642) |
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Nephrotic Syndrome [MESH:D009404] (1536) |
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Kidney Failure, Chronic [MESH:D007676] (2930) |
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Abortion, Spontaneous [MESH:D000022] (2780) |
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Diabetes, Gestational [MESH:D016640] (1157) |
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C14. Cardiovascular Diseases |
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C14. Cardiovascular Diseases |
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Tachycardia [MESH:D013610] (3339) |
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Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
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Diabetic Cardiomyopathies [MESH:D058065] (1995) |
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Aortic Valve Insufficiency [MESH:D001022] (1002) |
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Hypertension [MESH:D006973] (5655) |
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Aneurysm, Dissecting [MESH:D000784] (699) |
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Atherosclerosis [MESH:D050197] (4188) |
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Brain Ischemia [MESH:D002545] (4873) |
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Stroke [MESH:D020521] (3702) |
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Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
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Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
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Behcet Syndrome [MESH:D001528] (1784) |
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C15. Hemic and Lymphatic Diseases |
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C15. Hemic and Lymphatic Diseases |
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Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
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Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
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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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Spina Bifida Cystica [MESH:D016137] (209) |
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Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
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Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
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Amyloidosis, familial visceral [MESH:C538249] (285) |
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Hyperlipoproteinemia Type II [MESH:D006938] (707) |
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Familial HDL deficiency [MESH:C538394] (170) |
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Tangier Disease [MESH:D013631] (170) |
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Osteogenesis imperfecta, type 2A [MESH:C536042] (375) |
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Osteogenesis imperfecta, type 3 [MESH:C536044] (375) |
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Osteogenesis imperfecta, type 4 [MESH:C536045] (375) |
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Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
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Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
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Hernia, Umbilical [MESH:D006554] (115) |
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Hyperostosis, Cortical, Congenital [MESH:D006958] (392) |
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C17. Skin and Connective Tissue Diseases |
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C17. Skin and Connective Tissue Diseases |
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Keloid [MESH:D007627] (1111) |
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Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
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Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
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Osteogenesis imperfecta, type 2A [MESH:C536042] (375) |
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Osteogenesis imperfecta, type 3 [MESH:C536044] (375) |
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Osteogenesis imperfecta, type 4 [MESH:C536045] (375) |
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Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452) |
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Breast Neoplasms [MESH:D001943] (6077) |
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Drug Eruptions [MESH:D003875] (2697) |
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Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
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Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
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Ehlers-Danlos syndrome type 1 [MESH:C536194] (344) |
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Ehlers-Danlos Syndrome, Type VII, Autosomal Dominant [MESH:C562625] (375) |
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Behcet Syndrome [MESH:D001528] (1784) |
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C18. Nutritional and Metabolic Diseases |
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C18. Nutritional and Metabolic Diseases |
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Metabolic Syndrome X [MESH:D024821] (2151) |
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Calcinosis [MESH:D002114] (2989) |
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Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
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Diabetes, Gestational [MESH:D016640] (1152) |
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Metabolic Syndrome X [MESH:D024821] (2151) |
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Hypercholesterolemia [MESH:D006937] (1404) |
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Hyperlipoproteinemia Type II [MESH:D006938] (707) |
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Familial HDL deficiency [MESH:C538394] (170) |
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Tangier Disease [MESH:D013631] (170) |
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Amyloidosis, familial visceral [MESH:C538249] (285) |
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Hyperlipoproteinemia Type II [MESH:D006938] (707) |
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Familial HDL deficiency [MESH:C538394] (170) |
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Tangier Disease [MESH:D013631] (170) |
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Amyloidosis, familial visceral [MESH:C538249] (285) |
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Ataxia with vitamin E deficiency [MESH:C535393] (271) |
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Obesity, Morbid [MESH:D009767] (515) |
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C19. Endocrine System Diseases |
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C19. Endocrine System Diseases |
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Diabetes, Gestational [MESH:D016640] (1152) |
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Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
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Diabetic Cardiomyopathies [MESH:D058065] (1995) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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Hypogonadism [MESH:D007006] (1123) |
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Ovarian Neoplasms [MESH:D010051] (3281) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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C20. Immune System Diseases |
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C20. Immune System Diseases |
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Glomerulonephritis, Membranous [MESH:D015433] (642) |
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Hepatitis, Autoimmune [MESH:D019693] (1982) |
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Drug Eruptions [MESH:D003875] (2695) |
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HIV Infections [MESH:D015658] (3402) |
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C23. Pathological Conditions, Signs and Symptoms |
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C23. Pathological Conditions, Signs and Symptoms |
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Atrophy [MESH:D001284] (2603) |
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Hernia, Umbilical [MESH:D006554] (115) |
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Hypertrophy, Left Ventricular [MESH:D017379] (1430) |
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Gliosis [MESH:D005911] (1419) |
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Nerve Degeneration [MESH:D009410] (4061) |
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Tachycardia [MESH:D013610] (3339) |
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Sudden Infant Death [MESH:D013398] (268) |
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Nephrogenic Fibrosing Dermopathy [MESH:D054989] (452) |
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Keloid [MESH:D007627] (1110) |
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Sepsis [MESH:D018805] (3562) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Metastasis [MESH:D009362] (4441) |
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Edema [MESH:D004487] (3726) |
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Weight Gain [MESH:D015430] (2595) |
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Obesity, Morbid [MESH:D009767] (515) |
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Seizures [MESH:D012640] (4502) |
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Ataxia with vitamin E deficiency [MESH:C535393] (271) |
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Memory Disorders [MESH:D008569] (3233) |
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Learning Disorders [MESH:D007859] (2727) |
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Auditory Perceptual Disorders [MESH:D001308] (82) |
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Hyperalgesia [MESH:D006930] (3929) |
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Anoxia [MESH:D000860] (1698) |
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C25. Chemically-Induced Disorders |
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C25. Chemically-Induced Disorders |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Drug Eruptions [MESH:D003875] (2697) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Cocaine-Related Disorders [MESH:D019970] (3054) |
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Substance Withdrawal Syndrome [MESH:D013375] (2956) |
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Heroin Dependence [MESH:D006556] (950) |
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C26. Wounds and Injuries |
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C26. Wounds and Injuries |
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Radiation Injuries, Experimental [MESH:D011833] (2662) |
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D10. Lipids |
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D10. Lipids |
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Phosphatidylcholines [MESH:D010713] (257) |
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