more general categories |
information about this item |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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reaction (3393) |
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chemical synthesis (464) |
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reaction (1574) |
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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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Sepsis [MESH:D018805] (3556) |
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C04. Neoplasms |
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C04. Neoplasms |
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Carcinosarcoma [MESH:D002296] (581) |
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Carcinosarcoma [MESH:D002296] (581) |
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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Squamous Cell [MESH:D002294] (4294) |
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Papilloma [MESH:D010212] (2243) |
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Skin Neoplasms [MESH:D012878] (2992) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Lung Neoplasms [MESH:D008175] (6015) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Neoplasm Metastasis [MESH:D009362] (4441) |
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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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Acromicric dysplasia [MESH:C535662] (520) |
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Camurati-Engelmann Syndrome [MESH:D003966] (492) |
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Osteoporosis, Postmenopausal [MESH:D015663] (2351) |
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Intervertebral Disc Degeneration [MESH:D055959] (827) |
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Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
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Acromicric dysplasia [MESH:C535662] (520) |
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C06. Digestive System Diseases |
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C06. Digestive System Diseases |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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Duodenal Ulcer [MESH:D004381] (1549) |
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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, 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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Coproporphyria, Hereditary [MESH:D046349] (38) |
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Porphyria Cutanea Tarda [MESH:D017119] (766) |
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Porphyria, South African type [MESH:C538659] (48) |
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Cystic Fibrosis [MESH:D003550] (760) |
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Peritoneal Fibrosis [MESH:D056627] (488) |
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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Oral Submucous Fibrosis [MESH:D009914] (2432) |
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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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Cystic Fibrosis [MESH:D003550] (760) |
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Lung Neoplasms [MESH:D008175] (6012) |
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Pneumonia [MESH:D011014] (3482) |
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Pulmonary Fibrosis [MESH:D011658] (3140) |
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Berylliosis [MESH:D001607] (2005) |
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Asthma [MESH:D001249] (3903) |
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Pulmonary Emphysema [MESH:D011656] (1259) |
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Acute Lung Injury [MESH:D055371] (1907) |
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Berylliosis [MESH:D001607] (2005) |
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Asthma [MESH:D001249] (4098) |
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Pneumonia [MESH:D011014] (3482) |
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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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Stroke [MESH:D020521] (3702) |
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Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
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Diabetic Neuropathies [MESH:D003929] (2442) |
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C11. Eye Diseases |
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C11. Eye Diseases |
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Dry Eye Syndromes [MESH:D015352] (533) |
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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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Penile Induration [MESH:D010411] (495) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Diabetic Nephropathies [MESH:D003928] (2301) |
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Uremia [MESH:D014511] (2898) |
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Glomerulonephritis, IGA [MESH:D005922] (897) |
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Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
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Nephrotic Syndrome [MESH:D009404] (1536) |
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Kidney Failure, Chronic [MESH:D007676] (2930) |
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Ureteral Obstruction [MESH:D014517] (575) |
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Proteinuria [MESH:D011507] (3293) |
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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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Diabetic Nephropathies [MESH:D003928] (2301) |
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Uremia [MESH:D014511] (2898) |
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Glomerulonephritis, IGA [MESH:D005922] (897) |
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Glomerulosclerosis, Focal Segmental [MESH:D005923] (1754) |
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Nephrotic Syndrome [MESH:D009404] (1536) |
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Kidney Failure, Chronic [MESH:D007676] (2930) |
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Ureteral Obstruction [MESH:D014517] (575) |
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Proteinuria [MESH:D011507] (3293) |
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Abortion, Spontaneous [MESH:D000022] (2780) |
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C14. Cardiovascular Diseases |
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C14. Cardiovascular Diseases |
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Aortic Valve Insufficiency [MESH:D001022] (1002) |
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Myocardial Infarction [MESH:D009203] (4122) |
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Hypertension [MESH:D006973] (5655) |
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Stroke [MESH:D020521] (3702) |
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Myocardial Infarction [MESH:D009203] (4151) |
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C15. Hemic and Lymphatic Diseases |
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C15. Hemic and Lymphatic Diseases |
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Thrombocythemia, Essential [MESH:D013920] (707) |
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Thrombocythemia, Essential [MESH:D013920] (707) |
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Thrombocythemia, Essential [MESH:D013920] (707) |
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Thrombocythemia, Essential [MESH:D013920] (707) |
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Sarcoidosis [MESH:D012507] (895) |
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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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Acromicric dysplasia [MESH:C535662] (520) |
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Camurati-Engelmann Syndrome [MESH:D003966] (492) |
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Cystic Fibrosis [MESH:D003550] (760) |
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Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
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Coproporphyria, Hereditary [MESH:D046349] (38) |
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Porphyria Cutanea Tarda [MESH:D017119] (766) |
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Porphyria, South African type [MESH:C538659] (48) |
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Muscular Dystrophy, Duchenne [MESH:D020388] (942) |
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Coproporphyria, Hereditary [MESH:D046349] (38) |
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Porphyria Cutanea Tarda [MESH:D017119] (766) |
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Porphyria, South African type [MESH:C538659] (48) |
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Cystic Fibrosis [MESH:D003550] (760) |
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C17. Skin and Connective Tissue Diseases |
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C17. Skin and Connective Tissue Diseases |
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Penile Induration [MESH:D010411] (495) |
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Skin Neoplasms [MESH:D012878] (2991) |
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Coproporphyria, Hereditary [MESH:D046349] (38) |
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Porphyria Cutanea Tarda [MESH:D017119] (766) |
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Porphyria, South African type [MESH:C538659] (48) |
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Coproporphyria, Hereditary [MESH:D046349] (38) |
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Porphyria Cutanea Tarda [MESH:D017119] (766) |
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Porphyria, South African type [MESH:C538659] (48) |
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Urticaria [MESH:D014581] (2668) |
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C18. Nutritional and Metabolic Diseases |
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C18. Nutritional and Metabolic Diseases |
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Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
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Coproporphyria, Hereditary [MESH:D046349] (38) |
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Porphyria Cutanea Tarda [MESH:D017119] (766) |
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Porphyria, South African type [MESH:C538659] (48) |
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Coproporphyria, Hereditary [MESH:D046349] (38) |
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Porphyria Cutanea Tarda [MESH:D017119] (766) |
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Porphyria, South African type [MESH:C538659] (48) |
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Coproporphyria, Hereditary [MESH:D046349] (38) |
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Porphyria Cutanea Tarda [MESH:D017119] (766) |
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Porphyria, South African type [MESH:C538659] (48) |
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C19. Endocrine System Diseases |
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C19. Endocrine System Diseases |
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Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
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Diabetic Nephropathies [MESH:D003928] (2301) |
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Diabetic Neuropathies [MESH:D003929] (2443) |
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C20. Immune System Diseases |
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C20. Immune System Diseases |
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Glomerulonephritis, IGA [MESH:D005922] (897) |
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Hepatitis, Autoimmune [MESH:D019693] (1982) |
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Urticaria [MESH:D014581] (2668) |
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Asthma [MESH:D001249] (3914) |
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C23. Pathological Conditions, Signs and Symptoms |
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C23. Pathological Conditions, Signs and Symptoms |
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Ventricular Remodeling [MESH:D020257] (686) |
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Hernia, Diaphragmatic [MESH:D006548] (2647) |
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Hyperplasia [MESH:D006965] (2463) |
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Peritoneal Fibrosis [MESH:D056627] (488) |
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Sepsis [MESH:D018805] (3562) |
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Neoplasm Metastasis [MESH:D009362] (4441) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Proteinuria [MESH:D011507] (3293) |
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C24. Occupational Diseases |
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C24. Occupational Diseases |
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Berylliosis [MESH:D001607] (2005) |
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C25. Chemically-Induced Disorders |
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C25. Chemically-Induced Disorders |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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D03. Heterocyclic Compounds |
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D03. Heterocyclic Compounds |
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Protoporphyrins [MESH:D011524] (37) |
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Protoporphyrins [MESH:D011524] (37) |
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D04. Polycyclic Compounds |
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D04. Polycyclic Compounds |
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Protoporphyrins [MESH:D011524] (37) |
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D23. Biological Factors |
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D23. Biological Factors |
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Protoporphyrins [MESH:D011524] (37) |
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