All
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
 C16.320 Genetic Diseases, Inborn D030342 +
 C16.320.565 Metabolism, Inborn Errors D008661 +
 C16.320.565.618 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 +