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C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.565 Metabolism, Inborn Errors D008661 + C16.320.565.556 Lipid Metabolism, Inborn Errors D008052 + C16.320.565.556.641 Lipoidosis D008064 + C16.320.565.556.641.391 Lipoidproteinosis D008065 C16.320.565.556.641.509 Neuronal Ceroid-Lipofuscinosis D009472 C16.320.565.556.641.643 Refsum Disease D012035 C16.320.565.556.641.803 Sphingolipidoses D013106 + C16.320.565.556.641.201 Cholesterol Ester Storage Disease D015217 C16.320.565.556.641.923 Wolman Disease D015223 C16.320.565.556.641.723 Sjogren-Larsson Syndrome D016111
C18 Nutritional and Metabolic Diseases D009750 + C18.452 Metabolic Diseases D008659 + C18.452.648 Metabolism, Inborn Errors D008661 + C18.452.648.556 Lipid Metabolism, Inborn Errors D008052 + C18.452.648.556.641 Lipoidosis D008064 + C18.452.648.556.641.391 Lipoidproteinosis D008065 C18.452.648.556.641.509 Neuronal Ceroid-Lipofuscinosis D009472 C18.452.648.556.641.643 Refsum Disease D012035 C18.452.648.556.641.803 Sphingolipidoses D013106 + C18.452.648.556.641.201 Cholesterol Ester Storage Disease D015217 C18.452.648.556.641.923 Wolman Disease D015223 C18.452.648.556.641.723 Sjogren-Larsson Syndrome D016111