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C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.565 Metabolism, Inborn Errors D008661 + C16.320.565.580 Lysosomal Storage Diseases D016464 + C16.320.565.580.600 Mucopolysaccharidoses D009083 + C16.320.565.580.803 Sphingolipidoses D013106 + C16.320.565.580.201 Cholesterol Ester Storage Disease D015217 C16.320.565.580.923 Wolman Disease D015223 C16.320.565.580.554 Lysosomal Storage Diseases, Nervous System D020140 + C16.320.565.580.577 Mannosidase Deficiency Diseases D044904 +
C18 Nutritional and Metabolic Diseases D009750 + C18.452 Metabolic Diseases D008659 + C18.452.648 Metabolism, Inborn Errors D008661 + C18.452.648.595 Lysosomal Storage Diseases D016464 + C18.452.648.595.600 Mucopolysaccharidoses D009083 + C18.452.648.595.803 Sphingolipidoses D013106 + C18.452.648.595.201 Cholesterol Ester Storage Disease D015217 C18.452.648.595.923 Wolman Disease D015223 C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System D020140 + C18.452.648.595.577 Mannosidase Deficiency Diseases D044904 +