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C01. Bacterial Infections and Mycoses |
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C01. Bacterial Infections and Mycoses |
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Pasteurellaceae Infections [MESH:D016871] (348) |
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C04. Neoplasms |
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C04. Neoplasms |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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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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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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C10. Nervous System Diseases |
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C10. Nervous System Diseases |
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Dementia [MESH:D003704] (4498) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Parkinson Disease [MESH:D010300] (3595) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Dyskinesias [MESH:D020820] (1827) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Parkinson Disease [MESH:D010300] (3595) |
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Familial apoceruloplasmin deficiency [MESH:C536004] (211) |
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Parkinson Disease [MESH:D010300] (3595) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Ataxia [MESH:D001259] (1138) |
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C11. Eye Diseases |
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C11. Eye Diseases |
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Retinal Degeneration [MESH:D012162] (2386) |
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C12. Male Urogenital Diseases |
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C12. Male Urogenital Diseases |
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Albuminuria [MESH:D000419] (2394) |
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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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Albuminuria [MESH:D000419] (2394) |
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Pre-Eclampsia [MESH:D011225] (1435) |
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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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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Hemochromatosis [MESH:D006432] (1694) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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C17. Skin and Connective Tissue Diseases |
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C17. Skin and Connective Tissue Diseases |
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Psoriasis [MESH:D011565] (3278) |
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C18. Nutritional and Metabolic Diseases |
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C18. Nutritional and Metabolic Diseases |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
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Familial apoceruloplasmin deficiency [MESH:C536004] (211) |
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Hemochromatosis [MESH:D006432] (1694) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Hemochromatosis [MESH:D006432] (1694) |
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Hepatolenticular Degeneration [MESH:D006527] (473) |
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Deficiency Diseases [MESH:D003677] (2742) |
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C19. Endocrine System Diseases |
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C19. Endocrine System Diseases |
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Diabetes Mellitus, Type 1 [MESH:D003922] (1897) |
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C20. Immune System Diseases |
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C20. Immune System Diseases |
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Diabetes Mellitus, Type 1 [MESH:D003922] (1893) |
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C23. Pathological Conditions, Signs and Symptoms |
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C23. Pathological Conditions, Signs and Symptoms |
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Ischemia [MESH:D007511] (3049) |
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Nerve Degeneration [MESH:D009410] (4061) |
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Ataxia [MESH:D001259] (984) |
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Albuminuria [MESH:D000419] (2394) |
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D04. Polycyclic Compounds |
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D04. Polycyclic Compounds |
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Androstenes [MESH:D000736] (507) |
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D27. Chemical Actions and Uses |
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D27. Chemical Actions and Uses |
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Enzyme Inhibitors [MESH:D004791] (520) |
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Anticholesteremic Agents [MESH:D000924] (23) |
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Anticholesteremic Agents [MESH:D000924] (23) |
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