4.2.c

Peroxisomal biogenesis disorders

  • Peroxin 1 deficiency (Peroxisome biogenesis disorder 1A, Zellweger syndrome; peroxisome biogenesis disorder 1B, neonatal adrenoleukodystrophy/infantile Refsum disease; Heimler syndrome type 1)
  • Peroxin 2 deficiency (Peroxisome biogenesis disorder 5A, severe; peroxisome biogenesis disorder 5B, milder)
  • Peroxin 3 deficiency (Peroxisome biogenesis disorder 1A, severe; peroxisome biogenesis disorder 1B, milder)
  • Peroxin 5 deficiency (Rhizomelic chondrodysplasia punctata type 5)
  • Peroxin 6 deficiency (Peroxisome biogenesis disorder 5A, severe; peroxisome biogenesis disorder 5B, intermediate; Heimler syndrome type 2, milder)
  • Peroxin 10 deficiency (Peroxisome biogenesis disorder 6A, severe; peroxisome biogenesis disorder 6B, milder)
  • Peroxin 11B deficiency (Peroxisome biogenesis disorder 14B)
  • Peroxin 12 deficiency (Peroxisome biogenesis disorder 3A, severe; peroxisome biogenesis disorder 3B, milder)
  • Peroxin 13 deficiency (Peroxisome biogenesis disorder 11A, severe; peroxisome biogenesis disorder 11B, milder)
  • Peroxin 14 deficiency (Peroxisome biogenesis disorder 13A)
  • Peroxin 16 deficiency (Peroxisome biogenesis disorder 8A, severe; peroxisome biogenesis disorder 8B, milder)
  • Peroxin 19 deficiency (Peroxisome biogenesis disorder 12A)
  • Peroxin 26 deficiency (Peroxisome biogenesis disorder 7A, severe; peroxisome biogenesis disorder 7B, milder)

Subnetworks

PD 1 1

PD

Peroxisomal and lipid-related disorders

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