MeSH Browser

MeSH Supplementary: Peroxisomal ACYL-COA oxidase deficiency
Unique ID: C536662
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536662
Entry Term(s): Pseudoneonatal adrenoleukodystrophy; Straight-chain ACYL-COA oxidase deficiency
Heading Mapped to: *Adrenoleukodystrophy; *Lipid Metabolism, Inborn Errors; Acyl-CoA Oxidase / deficiency
Frequency: 1
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Peroxisomal ACYL-COA oxidase deficiency MeSH Supplementary Concept Data 2024