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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 +
C16.320.565.202 Carbohydrate Metabolism, Inborn Errors D002239 +
C16.320.565.202.607 Mannosidase Deficiency Diseases D044904 +
C16.320.565.202.607.750 beta-Mannosidosis D044905
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 +
C16.320.565.580.577 Mannosidase Deficiency Diseases D044904 +
C16.320.565.580.577.750 beta-Mannosidosis D044905
C18 Nutritional and Metabolic Diseases D009750 +
C18.452 Metabolic Diseases D008659 +
C18.452.648 Metabolism, Inborn Errors D008661 +
C18.452.648.202 Carbohydrate Metabolism, Inborn Errors D002239 +
C18.452.648.202.607 Mannosidase Deficiency Diseases D044904 +
C18.452.648.202.607.750 beta-Mannosidosis D044905
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 +
C18.452.648.595.577 Mannosidase Deficiency Diseases D044904 +
C18.452.648.595.577.750 beta-Mannosidosis D044905
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