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 glycoprotein degradation
                • Mannosidase deficiency diseases
                  • Alpha-mannosidosis (GDGDB) [MAN2B1]
                    • Alpha-mannosidosis, type II (later-onset) [MAN2B1]