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 +
 C16.320.565.618.711 Paralyses, Familial Periodic D010245 +
 C16.320.565.618.711.600 Paralysis, Hyperkalemic Periodic D020513