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
            • Other disorders of carbohydrate metabolism
              • Glycogen storage diseases
                • Pompe disease (GDGDB) [GAA]
                  • Pompe disease, infantile-onset form [GAA]
                  • Pompe disease, late-onset form [GAA]