peroxisomal biogenesis factor 2

Preferred Label : peroxisomal biogenesis factor 2;

Approved symbol HGNC : PEX2;

Name synonyms HGNC : peroxin 2; Zellweger syndrome;

Alias symbols HGNC : ZWS3; PAF-1; RNF72; PMP35;

Chromosome HGNC : 8q21.13;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000164751;

Détails

Origin ID

HGNC:9717;

UMLS CUI

C1419149;

Automatic exact mappings (from CISMeF team)
- Peroxisomal Biogenesis Factor 2 [MeSH Descriptor]
- Peroxisomal Biogenesis Factor 2 [MeSH concept]
- Peroxisome biogenesis factor 2 [OMIM gene]
- Zellweger Syndrome [NCIt concept]
- Zellweger syndrome [ICD-11 More detail]
- Zellweger syndrome [ORDO Disease]
- Zellweger syndrome [MedDRA LLT]
- Zellweger syndrome [DO Concept]
- Zellweger syndrome (disorder) [SNOMED CT concept]
- peroxisomal biogenesis factor 2 [ORDO Gene]
- zellweger syndrome [MeSH Descriptor]
- zellweger syndrome [MeSH concept]
- zellweger syndrome [SNOMED Notion]
NCIt concept
- PEX2 Gene [NCIt concept]
OMIM gene
- Peroxisome biogenesis factor 2 [OMIM gene]
Orphanet gene
- peroxisomal biogenesis factor 2 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PEX2 Gene [NCIt concept]
- PEX2 gene [LOINC component]
- Peroxisome biogenesis factor 2 [OMIM gene]

Position du mot-clé dans l'(les) arborescence(s) :

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