Legend:

• Concept Types
  • target (clinical findings)
  • classification term
  • pathway-based classification term
  • clinical findings
  • multiple types disease
  • single disease
  • disease type

• Congenital, Hereditary, and Neonatal Diseases and Abnormalities related to Glycans
  • Genetic Diseases, Inborn
    • Metabolism, Inborn Errors
      • Carbohydrate Metabolism, Inborn Errors (synthesis)
        • Hereditary disorders by systems
          • Genetic disorders of glycan synthesis (by systems, signs and symptoms)
            • Diseases
              • Neoplasms
                • Neoplasms by Histologic Type
                  • Neoplasms, Connective and Soft Tissue
                    • Neoplasms, Connective Tissue
                      • Neoplasms, Bone Tissue
                        • Osteochondroma
                          • Osteochondromatosis
                            • Exostoses, Multiple Hereditary
                              • EXT1/EXT2-CDG [EXT1,EXT2]
                • Neoplastic Syndromes, Hereditary
                  • Exostoses, Multiple Hereditary
                    • EXT1/EXT2-CDG [EXT1,EXT2]
      • Lysosomal Storage Diseases (degradation)
        • Hereditary disorders by systems
          • Genetic disorders of glycan degradation (by systems, signs and symptoms)
            • Diseases
              • Neoplasms
                • Neoplasms by Histologic Type
                  • Neoplasms, Vascular Tissue
                    • Angiokeratoma
                      • Fucosidosis (GDGDB) [FUCA1]
                      • Beta-mannosidosis (GDGDB) [MANBA]
                      • Sialidosis (GDGDB) [NEU1]
                      • Schindler disease, type II (GDGDB) [NAGA]
                      • Galactosialidosis (GDGDB) [CTSA]
                      • Fabry disease (GDGDB) [GLA]