Peroxisomal straight-chain acyl-CoA oxidase deficiency

Synonym(s)
- Pseudo-neonatal adrenoleukodystrophy
Type

Disease
External link(s)
- Orphanet
- IEMbase
Gene
- ACOX1 / Acyl-CoA Oxidase 1
  17q25.1
  OMIM
  GnomAD
  Ensembl
  HGNC
  VMH
  LOVD
Gene product
- Peroxisomal acyl-coenzyme A oxidase 1
Disease group(s)
- 14.2 Disorders of peroxisomal fatty acid oxidation
Child entries
- Mitchell Syndrome