Periaxin - CISMeF

Preferred Label : Periaxin;

Symbol : PRX;

CISMeF acronym : PRX;

Type : Gene;

Ensembl ID : ENSG00000105227;

Prefixed ID : *605725;

Details

Origin ID

605725;

UMLS CUI

C1422198;

Automatic exact mappings (from CISMeF team)
- PRX gene [LOINC component]
- periaxin [ORDO Gene]
- periaxin [MeSH concept]
- periaxin [MeSH Supplementary Concept]
- periaxin [HGNC gene]
- peroxiredoxin 6 [HGNC gene]
HGNC gene
- periaxin [HGNC gene]
ORDO concept(s)
- periaxin [ORDO Gene]
Phenotypes related
- Charcot-marie-tooth disease, demyelinating, type 4f [OMIM Phenotype]
- Hypertrophic neuropathy of dejerine-sottas [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PRX gene [LOINC component]
- periaxin [HGNC gene]

Keyword's position in hierarchy(ies) :

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