All
 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
 C16.320 Genetic Diseases, Inborn D030342 +
 C16.320.565 Metabolism, Inborn Errors D008661 +
 C16.320.565.437 Hyperbilirubinemia, Hereditary D006933 +
 C16.320.565.437.281 Crigler-Najjar Syndrome D003414 
 C16.320.565.437.528 Gilbert Disease D005878