Legend:

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

'Seizures'  (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
      • Central Nervous System Diseases
        • Brain Diseases
          • Epilepsy
            • Seizures
              • ST3GAL5-CDG [SIAT9]
      • Neurologic Manifestations
        • Seizures
          • PMM2-CDG (GDGDB) [PMM2]
            • PMM2-CDG, infantile multisystem stage [PMM2]
            • PMM2-CDG, late-infantile and childhood ataxia-intellectual disability stage [PMM2]
            • PMM2-CDG, adult stable disability stage [PMM2]
          • ALG6-CDG (GDGDB) [ALG6]
          • ALG3-CDG (GDGDB) [ALG3]
          • DPM1-CDG (GDGDB) [DPM1]
          • MPDU1-CDG (GDGDB) [MPDU1]
          • ALG12-CDG (GDGDB) [ALG12]
          • ALG8-CDG (GDGDB) [ALG8]
          • ALG2-CDG (GDGDB) [ALG2]
          • DPAGT1-CDG (GDGDB) [DPAGT1]
          • ALG1-CDG (GDGDB) [ALG1]
          • ALG9-CDG (GDGDB) [ALG9]
          • DOLK-CDG [TMEM15]
          • RFT1-CDG [RFT1]
          • MGAT2-CDG (GDGDB) [MGAT2]
          • GCS1-CDG (GDGDB) [GCS1]
          • SLC35C1-CDG (GDGDB) [SLC35C1]
          • COG7-CDG (GDGDB) [COG7]
          • COG8-CDG [COG8]
          • COG4-CDG [COG4]
          • ATP6VOA2-CDG [ATP6V0A2]
          • POMT1/POMT2-CDG (cong. muscular dystrophy spectrum) (GDGDB) [POMT1,POMT2]
          • POMGNT1-CDG (cong. muscular dystrophy spectrum) (GDGDB) [POMGNT1]
          • Fukuyama congenital muscular dystrophy (GDGDB) [FKTN]
          • ST3GAL5-CDG [SIAT9]
          • PIGM-CDG [PIGM]
          • ALG11-CDG [ALG11]
          • ALG13-CDG [ALG13]
          • COG6-CDG [COG6]
          • Mental retardation, autosomal recessive 15 [MAN1B1]
          • Hyperphosphatasia with mental retardation syndrome 1 [PIGV]
          • Multiple congenital anomalies-hypotonia-seizures syndrome 1 [PIGN]