All

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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 +
    C16.320.565.618 Metal Metabolism, Inborn Errors D008664 +
      C16.320.565.618.337 Hemochromatosis D006432 
      C16.320.565.618.403 Hepatolenticular Degeneration D006527 
      C16.320.565.618.482 Hypophosphatasia D007014 
      C16.320.565.618.544 Hypophosphatemia, Familial D007015 
      C16.320.565.618.590 Menkes Kinky Hair Syndrome D007706 
      C16.320.565.618.711 Paralyses, Familial Periodic D010245 +
      C16.320.565.618.815 Pseudohypoparathyroidism D011547 +
 C18 Nutritional and Metabolic Diseases D009750 +
  C18.452 Metabolic Diseases D008659 +
   C18.452.648 Metabolism, Inborn Errors D008661 +
    C18.452.648.618 Metal Metabolism, Inborn Errors D008664 +
      C18.452.648.618.337 Hemochromatosis D006432 
      C18.452.648.618.403 Hepatolenticular Degeneration D006527 
      C18.452.648.618.482 Hypophosphatasia D007014 
      C18.452.648.618.544 Hypophosphatemia, Familial D007015 
      C18.452.648.618.590 Menkes Kinky Hair Syndrome D007706 
      C18.452.648.618.711 Paralyses, Familial Periodic D010245 +
      C18.452.648.618.815 Pseudohypoparathyroidism D011547 +