All
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
 C16.320 Genetic Diseases, Inborn D030342 +
 C16.320.565 Metabolism, Inborn Errors D008661 +
 C16.320.565.066 Amino Acid Metabolism, Inborn Errors D000592 +
 C16.320.565.066.275 Carbamoyl-Phosphate Synthase I Deficiency Disease D020165