Legend:

• Concept Types

• 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
              • Eye Diseases
                • Ocular Motility Disorders
                  • Nystagmus, Pathologic
                    • Nystagmus, Congenital
                      • DPM1-CDG (GDGDB) [DPM1]
                      • DOLK-CDG [TMEM15]
                      • COG4-CDG [COG4]
                      • SRD5A3-CDG [SRD5A3]
                      • ALG13-CDG [ALG13]
                      • Multiple congenital anomalies-hypotonia-seizures syndrome 1 [PIGN]
              • Nervous System Diseases
                • Cranial Nerve Diseases
                  • Ocular Motility Disorders
                    • Nystagmus, Pathologic
                      • Nystagmus, Congenital
                        • DPM1-CDG (GDGDB) [DPM1]
                        • DOLK-CDG [TMEM15]
                        • COG4-CDG [COG4]
                        • SRD5A3-CDG [SRD5A3]
                        • ALG13-CDG [ALG13]
                        • Multiple congenital anomalies-hypotonia-seizures syndrome 1 [PIGN]