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
              • Female Urogenital Diseases and Pregnancy Complications
                • Female Urogenital Diseases
                  • Urologic Diseases
                    • Kidney Diseases
                      • Kidney Diseases, Cystic
                        • PMM2-CDG (GDGDB) [PMM2]
                          • PMM2-CDG, infantile multisystem stage [PMM2]
                        • ALG9-CDG (GDGDB) [ALG9]
                      • Nephrosis
                        • Nephrotic Syndrome
                          • PMM2-CDG (GDGDB) [PMM2]
                            • PMM2-CDG, infantile multisystem stage [PMM2]
                          • ALG1-CDG (GDGDB) [ALG1]
                        • COG6-CDG [COG6]
                        • Ehlers-Danlos syndrome, musculocontractural type [CHST14]
                        • Multiple congenital anomalies-hypotonia-seizures syndrome 1 [PIGN]
                    • Multiple congenital anomalies-hypotonia-seizures syndrome 1 [PIGN]
              • Male Urogenital Diseases
                • Urologic Diseases
                  • Kidney Diseases
                    • Kidney Diseases, Cystic
                      • PMM2-CDG (GDGDB) [PMM2]
                        • PMM2-CDG, infantile multisystem stage [PMM2]
                      • ALG9-CDG (GDGDB) [ALG9]
                    • Nephrosis
                      • Nephrotic Syndrome
                        • PMM2-CDG (GDGDB) [PMM2]
                          • PMM2-CDG, infantile multisystem stage [PMM2]
                        • ALG1-CDG (GDGDB) [ALG1]
                      • COG6-CDG [COG6]
                      • Ehlers-Danlos syndrome, musculocontractural type [CHST14]
                      • Multiple congenital anomalies-hypotonia-seizures syndrome 1 [PIGN]
                  • Multiple congenital anomalies-hypotonia-seizures syndrome 1 [PIGN]
      • Lysosomal Storage Diseases (degradation)
        • Hereditary disorders by systems
          • Genetic disorders of glycan degradation (by systems, signs and symptoms)
            • Diseases
              • Female Urogenital Diseases and Pregnancy Complications
                • Female Urogenital Diseases
                  • Urologic Diseases
                    • Kidney Diseases
                      • Galactosialidosis (GDGDB) [CTSA]
                      • Fabry disease (GDGDB) [GLA]
                      • Renal Insufficiency
                        • Galactosialidosis (GDGDB) [CTSA]
                        • Fabry disease (GDGDB) [GLA]
              • Male Urogenital Diseases
                • Urologic Diseases
                  • Kidney Diseases
                    • Galactosialidosis (GDGDB) [CTSA]
                    • Fabry disease (GDGDB) [GLA]
                    • Renal Insufficiency
                      • Galactosialidosis (GDGDB) [CTSA]
                      • Fabry disease (GDGDB) [GLA]