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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 +
C16.320.565.556.475 Hypercholesterolemia, Familial D006938
C16.320.565.556.480 Hyperlipidemia, Familial Combined D006950 +
C16.320.565.556.483 Hyperlipoproteinemia Type III D006952
C16.320.565.556.487 Hyperlipoproteinemia Type IV D006953
C16.320.565.556.493 Hyperlipoproteinemia Type V D006954
C16.320.565.556.500 Hypolipoproteinemia D007009 +
C16.320.565.556.641 Lipoidosis D008064 +
C16.320.565.556.645 Lipoprotein Lipase Deficiency, Familial D008072
C16.320.565.556.750 Peroxisomal Disorders D018901 +
C16.320.565.556.850 Smith-Lemli-Opitz Syndrome D019082
C16.320.565.556.925 Xanthomatosis, Cerebrotendinous D019294
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 +
C18.452.648.556.475 Hypercholesterolemia, Familial D006938
C18.452.648.556.480 Hyperlipidemia, Familial Combined D006950 +
C18.452.648.556.484 Hyperlipoproteinemia Type III D006952
C18.452.648.556.490 Hyperlipoproteinemia Type IV D006953
C18.452.648.556.495 Hyperlipoproteinemia Type V D006954
C18.452.648.556.500 Hypolipoproteinemia D007009 +
C18.452.648.556.641 Lipoidosis D008064 +
C18.452.648.556.645 Lipoprotein Lipase Deficiency, Familial D008072
C18.452.648.556.750 Peroxisomal Disorders D018901 +
C18.452.648.556.850 Smith-Lemli-Opitz Syndrome D019082
C18.452.648.556.925 Xanthomatosis, Cerebrotendinous D019294
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