peroxisome biogenesis disorder, complementation group E

Preferred Label : peroxisome biogenesis disorder, complementation group E;

Origin ID

C566569;

UMLS CUI

C1865804;

Automatic exact mappings (from CISMeF team)
- Peroxisome biogenesis disorder 1a (zellweger) [OMIM Phenotype]
MeSH term(s) associated for indexing
- peroxisomal disorders [MeSH Descriptor]
Record concept(s)
- peroxisome biogenesis disorder, complementation group E [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]