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)
            • Psychiatry and Psychology
              • Behavior and Behavior Mechanisms
                • Emotions
                  • Affect
                    • Irritable Mood
                      • ST3GAL5-CDG [SIAT9]
      • Lysosomal Storage Diseases (degradation)
        • Hereditary disorders by systems
          • Genetic disorders of glycan degradation (by systems, signs and symptoms)
            • Psychiatry and Psychology
              • Behavior and Behavior Mechanisms
                • Behavior
                  • Behavioral Symptoms
                    • Child Reactive Disorders
                      • Beta-mannosidosis (GDGDB) [MANBA]
                    • Delusions
                      • Metachromatic leukodystrophy (GDGDB) [ARSA]
                        • Metachromatic leukodystrophy, adult form [ARSA]
                    • Depression
                      • Alpha-mannosidosis (GDGDB) [MAN2B1]
                      • Beta-mannosidosis (GDGDB) [MANBA]
                    • Aspartylglucosaminuria (GDGDB) [AGA]
                    • Alpha-mannosidosis (GDGDB) [MAN2B1]
                    • Beta-mannosidosis (GDGDB) [MANBA]
                    • Metachromatic leukodystrophy (GDGDB) [ARSA]
                    • Metachromatic leukodystrophy, due to saposin B deficiency (GDGDB) [PSAP]
                    • Niemann-Pick disease, type C1 (GDGDB) [NPC1]
                    • Niemann-Pick disease, type C2 (GDGDB) [NPC2]