(Q18553481)
English
peroxisomal acyl-CoA oxidase deficiency
peroxisomal disease that is characterized by hypotonia and seizures in the neonatal period and neurological regression in early infancy
- Peroxisomal acyl-coenzyme A oxidase
- Pseudoneonatal Adrenoleukodystrophy
- Straight-Chain Acyl-Coa Oxidase Deficiency
- Pseudoadrenoleukodystrophy
- Pseudo-neonatal adrenoleukodystrophy
- Pseudo-NALD
- PEROXISOMAL ACYL-CoA OXIDASE DEFICIENCY
- Acyl-CoA oxidase deficiency
Statements
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255.41
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C170437
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Identifiers
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Sitelinks
Wikipedia(1 entry)
- enwiki Acyl-CoA oxidase deficiency