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
              • Pathological Conditions, Signs and Symptoms
                • Pathological Conditions, Anatomical
                  • Hernia
                    • Hernia, Abdominal
                      • Hernia, Ventral
                        • Hernia, Umbilical
                          • Achondrogenesis type IB [SLC26A2]
      • Lysosomal Storage Diseases (degradation)
        • Hereditary disorders by systems
          • Genetic disorders of glycan degradation (by systems, signs and symptoms)
            • Diseases
              • Pathological Conditions, Signs and Symptoms
                • Pathological Conditions, Anatomical
                  • Hernia
                    • Hernia, Abdominal
                      • Hernia, Ventral
                        • Hernia, Umbilical
                          • Mucolipidosis II (alpha/beta) (GDGDB) [GNPTAB]
                          • Hurler syndrome (GDGDB) [IDUA]
                          • Hurler-Scheie syndrome (GDGDB) [IDUA]
                          • Scheie syndrome (GDGDB) [IDUA]
                          • Mucopolysaccharidosis II (GDGDB) [IDS]
                          • Sanfilippo syndrome A (GDGDB) [SGSH]
                          • Sanfilippo syndrome B (GDGDB) [NAGLU]
                          • Sanfilippo syndrome C (GDGDB) [HGSNAT]
                          • Sanfilippo syndrome D (GDGDB) [GNS]
                          • Morquio syndrome A (GDGDB) [GALNS]
                          • Morquio syndrome B (GDGDB) [GLB1]
                          • Mucopolysaccharidosis VI (GDGDB) (GDGDB) [ARSB]
                          • Mucopolysaccharidosis VII (GDGDB) [GUSB]