peroxisome biogenesis disorder, complementation group 4

Preferred Label : peroxisome biogenesis disorder, complementation group 4;

MeSH note : Peroxisome biogenesis disorders CG4, CG6, and CGC share impaired PEX6 function and PXAAA1 gene variation.;

CISMeF synonym : peroxisome biogenesis disorder, complementation group 6; peroxisome biogenesis disorder, complementation group C;

Details

Origin ID

C563301;

UMLS CUI

C1832230;

Automatic exact mappings (from CISMeF team)
- Peroxisome biogenesis disorder 4a (zellweger) [OMIM Phenotype]
MeSH term(s) associated for indexing
- peroxisomal disorders [MeSH Descriptor]
Record concept(s)
- peroxisome biogenesis disorder, complementation group 4 [MeSH concept]
- peroxisome biogenesis disorder, complementation group 6 [MeSH concept]
- peroxisome biogenesis disorder, complementation group C [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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