Legend:

• Concept Types

'Neurodegenerative 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
    • Nervous System Diseases
      • Neurodegenerative Diseases
        • Heredodegenerative Disorders, Nervous System
          • PMM2-CDG (GDGDB) [PMM2]
            • PMM2-CDG, infantile multisystem stage [PMM2]
            • PMM2-CDG, late-infantile and childhood ataxia-intellectual disability stage [PMM2]
          • ALG3-CDG (GDGDB) [ALG3]
          • ALG1-CDG (GDGDB) [ALG1]
          • ALG9-CDG (GDGDB) [ALG9]
          • COG7-CDG (GDGDB) [COG7]
          • COG1-CDG [COG1]
          • COG8-CDG [COG8]
          • COG5-CDG [COG5]
          • COG4-CDG [COG4]
          • ATP6VOA2-CDG [ATP6V0A2]
          • B3GALTL-CDG [B3GALTL]
          • ST3GAL5-CDG [SIAT9]
          • SRD5A3-CDG [SRD5A3]
          • DDOST-CDG [DDOST]
          • ALG13-CDG [ALG13]
          • TMEM165-CDG [TMEM165]
          • Hyperphosphatasia with mental retardation syndrome 1 [PIGV]
          • Multiple congenital anomalies-hypotonia-seizures syndrome 1 [PIGN]