Legend:

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

'Gastrointestinal Diseases'  (Integration tree)

Pathogenesis (traditional nomenclature)

• Genetic disorders of glycan synthesis (traditional nomenclature)

Pathogenesis (new nomenclature)

• Genetic disorders of glycan synthesis (new nomenclature)

Genetic disorders of glycan synthesis (by systems, signs and symptoms)

• Genetic disorders of glycan synthesis (by systems, signs and symptoms)
  • Diseases
    • Digestive System Diseases
      • Gastrointestinal Diseases
        • Esophageal Diseases
          • Deglutition Disorders
            • Esophageal Motility Disorders
              • Esophageal Spasm, Diffuse
                • Paroxysmal nocturnal hemoglobinuria, somatic (SOMATIC MUTATION) (GDGDB) [PIGA]
        • Intestinal Diseases
          • Protein-Losing Enteropathies
            • MPI-CDG (GDGDB) [MPI]
            • ALG6-CDG (GDGDB) [ALG6]
            • ALG8-CDG (GDGDB) [ALG8]
          • ALG8-CDG (GDGDB) [ALG8]
        • Gastrointestinal Hemorrhage
          • MPI-CDG (GDGDB) [MPI]
          • ALG11-CDG [ALG11]
        • COG6-CDG [COG6]
        • Ehlers-Danlos syndrome, musculocontractural type [CHST14]
        • Multiple congenital anomalies-hypotonia-seizures syndrome 1 [PIGN]