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Up to: Inherited lipid metabolism disorder · Peroxisomal single enzyme/protein defect

Disorder of plasmalogens biosynthesis

0 trials tagged with this condition →

  • Rhizomelic chondrodysplasia punctata 2 trials Sub-types →
  • Acyl-CoA binding domain containing protein 5 deficiency 1 trial
  • Alkylglycerone-phosphate synthase deficiency 0 trials · 1 incl. sub-types Sub-types →
  • Glyceronephosphate O-acyltransferase deficiency 0 trials · 1 incl. sub-types Sub-types →
  • Fatty acyl-CoA reductase defects 0 trials Sub-types →

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