peroxisome biogenesis disorder, complementation group H

Preferred Label : peroxisome biogenesis disorder, complementation group H;

Origin ID

C566626;

UMLS CUI

C1866260;

Automatic exact mappings (from CISMeF team)
- Peroxisome biogenesis disorder 11a (zellweger) [OMIM Phenotype]
MeSH term(s) associated for indexing
- peroxisomal disorders [MeSH Descriptor]
Record concept(s)
- peroxisome biogenesis disorder, complementation group H [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]