Legend:

• Concept Types

• Congenital, Hereditary, and Neonatal Diseases and Abnormalities related to Glycans
  • Genetic Diseases, Inborn
    • Metabolism, Inborn Errors
      • Lysosomal Storage Diseases (degradation)
        • Pathogenesis
          • Genetic disorders of glycan degradation
            • Disorders of glycoprotein metabolism
              • Defects in post-translational modification of lysosomal enzymes
                • Mucolipidosis II (alpha/beta) (GDGDB) [GNPTAB]
                • Mucolipidosis III (alpha/beta) (GDGDB) [GNPTAB]