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
              • Hemic and Lymphatic Diseases
                • Hematologic Diseases
                  • Anemia
                    • Anemia, Hemolytic
                      • Hemoglobinuria, Paroxysmal
                        • Paroxysmal nocturnal hemoglobinuria, somatic (SOMATIC MUTATION) (GDGDB) [PIGA]
                      • Anemia, Hemolytic, Congenital
                        • Anemia, Dyserythropoietic, Congenital
                          • SEC23B-CDG (GDGDB) [SEC23B]
                      • Anemia, Hemolytic, Autoimmune
                        • Tn polyagglutination syndrome, somatic (SOMATIC MUTATION) [C1GALT1C1]
                    • ALG8-CDG (GDGDB) [ALG8]
                    • DPAGT1-CDG (GDGDB) [DPAGT1]
                    • SEC23B-CDG (GDGDB) [SEC23B]
                    • SRD5A3-CDG [SRD5A3]
      • Lysosomal Storage Diseases (degradation)
        • Hereditary disorders by systems
          • Genetic disorders of glycan degradation (by systems, signs and symptoms)
            • Diseases
              • Hemic and Lymphatic Diseases
                • Hematologic Diseases
                  • Anemia
                    • Gaucher disease, type I (GDGDB) [GBA]
                    • Gaucher disease, type II (GDGDB) [GBA]
                    • Gaucher disease, type III (GDGDB) [GBA]
                    • Wolman disease (GDGDB) [LIPA]