(Q18553313)

English

congenital disorder of glycosylation type I

congenital disorder of glycosylation involve disrupted synthesis of the lipid-linked oligosaccharide precursor

  • ALG1-CDG (CDG-1k)
  • ALG11-CDG (CDG-1p)
  • ALG12-CDG (CDG-1g)
  • ALG2-CDG (CDG-1i)
  • ALG3-CDG (CDG-1d)
  • ALG6-CDG (CDG-1c)
  • ALG8-CDG (CDG-1h)
  • ALG9-CDG (CDG-1l)
  • DOLK-CDG (CDG-1m)
  • DPAGT1-CDG (CDG-1j)
  • DPM1-CDG (CDG-1e)
  • DPM2-CDG (CDG-1u)
  • DPM3-CDG (CDG-1o)
  • MPDU1-CDG (CDG-1f)
  • MPI-CDG (CDG-1b)
  • PMM2-CDG (CDG-1a)
  • RFT1-CDG (CDG-1n)
  • SRD5A3-CDG (CDG-1q)
  • ALG9-CDG
  • ALG12-CDG
  • DOLK-CDG
  • ALG11-CDG
  • SRD5A3-CDG
  • DPM1-CDG
  • ALG2-CDG
  • RFT1-CDG
  • ALG1-CDG
  • ALG3-CDG
  • ALG8-CDG
  • DPAGT1-CDG
  • MPDU1-CDG
  • MPI-CDG
  • ALG6-CDG
  • DPM3-CDG
  • PMM2-CDG
  • DPM2-CDG
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