MeSH Browser

MeSH Supplementary: Peroxisome Biogenesis Disorder, Complementation Group 4
Unique ID: C563301
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563301
Entry Term(s): Peroxisome Biogenesis Disorder, Complementation Group 6; Peroxisome Biogenesis Disorder, Complementation Group C
Registry Numbers: 0
Heading Mapped to: *Peroxisomal Disorders
Frequency: 0
Note: Peroxisome biogenesis disorders CG4, CG6, and CGC share impaired PEX6 function and PXAAA1 gene variation.
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Peroxisome Biogenesis Disorder, Complementation Group 4 MeSH Supplementary Concept Data 2025