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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potassium voltage-gated channel, Isk-related family, member 1 [HGNC:KCNE1] (19) |
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potassium voltage-gated channel, KQT-like subfamily, member 1 [HGNC:KCNQ1] (21) |
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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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activity (2549) |
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A. Anatomy |
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A. Anatomy |
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Short QT Syndrome 3 [MESH:C566504] (39) |
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Short QT Syndrome 2 [MESH:C566505] (45) |
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C04. Neoplasms |
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C04. Neoplasms |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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C09. Otorhinolaryngologic Diseases |
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C09. Otorhinolaryngologic Diseases |
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Hearing Loss, Noise-Induced [MESH:D006317] (134) |
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C10. Nervous System Diseases |
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C10. Nervous System Diseases |
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Spasm [MESH:D013035] (418) |
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Hearing Loss, Noise-Induced [MESH:D006317] (134) |
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Hyperalgesia [MESH:D006930] (3929) |
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Arsenic Poisoning [MESH:D020261] (2540) |
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C14. Cardiovascular Diseases |
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C14. Cardiovascular Diseases |
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Short QT Syndrome 3 [MESH:C566504] (39) |
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Short QT Syndrome 2 [MESH:C566505] (45) |
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Cardiomyopathies [MESH:D009202] (5331) |
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Short QT Syndrome 3 [MESH:C566504] (39) |
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Short QT Syndrome 2 [MESH:C566505] (45) |
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Atrial Flutter [MESH:D001282] (44) |
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Ventricular Fibrillation [MESH:D014693] (624) |
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Atrial Fibrillation, Familial, 3 [MESH:C563817] (60) |
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Long Qt Syndrome 5 [MESH:C566766] (40) |
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Andersen Syndrome [MESH:D050030] (39) |
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Jervell-Lange Nielsen Syndrome [MESH:D029593] (64) |
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Romano-Ward Syndrome [MESH:D029597] (47) |
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Tachycardia, Ventricular [MESH:D017180] (1386) |
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Short QT Syndrome 3 [MESH:C566504] (39) |
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Short QT Syndrome 2 [MESH:C566505] (45) |
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Hypertension [MESH:D006973] (5655) |
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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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Short QT Syndrome 3 [MESH:C566504] (39) |
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Short QT Syndrome 2 [MESH:C566505] (45) |
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Long Qt Syndrome 5 [MESH:C566766] (40) |
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Andersen Syndrome [MESH:D050030] (39) |
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Jervell-Lange Nielsen Syndrome [MESH:D029593] (64) |
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Romano-Ward Syndrome [MESH:D029597] (47) |
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C17. Skin and Connective Tissue Diseases |
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C17. Skin and Connective Tissue Diseases |
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Skin Diseases [MESH:D012871] (8774) |
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C18. Nutritional and Metabolic Diseases |
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C18. Nutritional and Metabolic Diseases |
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Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
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C19. Endocrine System Diseases |
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C19. Endocrine System Diseases |
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Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
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C23. Pathological Conditions, Signs and Symptoms |
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C23. Pathological Conditions, Signs and Symptoms |
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Gliosis [MESH:D005911] (1419) |
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Nerve Degeneration [MESH:D009410] (4061) |
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Short QT Syndrome 3 [MESH:C566504] (39) |
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Short QT Syndrome 2 [MESH:C566505] (45) |
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Atrial Flutter [MESH:D001282] (44) |
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Ventricular Fibrillation [MESH:D014693] (624) |
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Atrial Fibrillation, Familial, 3 [MESH:C563817] (60) |
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Long Qt Syndrome 5 [MESH:C566766] (40) |
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Andersen Syndrome [MESH:D050030] (39) |
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Romano-Ward Syndrome [MESH:D029597] (47) |
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Tachycardia, Ventricular [MESH:D017180] (1386) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Spasm [MESH:D013035] (418) |
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Hearing Loss, Noise-Induced [MESH:D006317] (134) |
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Hyperalgesia [MESH:D006930] (3929) |
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C25. Chemically-Induced Disorders |
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C25. Chemically-Induced Disorders |
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Arsenic Poisoning [MESH:D020261] (2540) |
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D01. Inorganic Chemicals |
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D01. Inorganic Chemicals |
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Barium Compounds [MESH:D017609] (31) |
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Chlorides [MESH:D002712] (118) |
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Chlorides [MESH:D002712] (57) |
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