All
 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