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 +
 C16.320.565.066.102 Albinism D000417 +
 C16.320.565.066.102.100 Albinism, Oculocutaneous D016115 +
 C16.320.565.066.102.100.400 Hermanski-Pudlak Syndrome D022861