Peroxisome Biogenesis Disorder 4B

Preferred Label : Peroxisome Biogenesis Disorder 4B;

NCIt synonyms : PBD4B;

NCIt definition : An autosomal recessive condition caused by mutation(s) in the PEX6 gene, peroxisome assembly factor 2, Peroxisome biogenesis disorder 4B is characterized by overlapping phenotypes of neonatal adrenoleukodystrophy and infantile Refsum disease.;

Details

Origin ID

C155755;

UMLS CUI

C3553937;

CISMeF manual mappings
- Peroxisome biogenesis disorder 4b [OMIM Phenotype]
Has associated anatomic sites
- Nervous System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Peroxisome biogenesis disorder 4b [OMIM Phenotype]
disease_has_finding
- Rare Lesion [NCIt concept]
disease_mapped_to_gene
- PEX6 Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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