peripheral myelin protein 22

Preferred Label : peripheral myelin protein 22;

Approved symbol HGNC : PMP22;

Alias symbols HGNC : Sp110; HNPP; HMSNIA; GAS3;

Chromosome HGNC : 17p12;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000109099;

Details

Origin ID

HGNC:9118;

UMLS CUI

C1418677;

Automatic exact mappings (from CISMeF team)
- Neuropathy, hereditary, with liability to pressure palsies [OMIM Phenotype]
- Peripheral Myelin Protein 22 [NCIt concept]
- Peripheral myelin protein 22 [OMIM gene]
- peripheral myelin protein 22 [ORDO Gene]
NCIt concept
- PMP22 Gene [NCIt concept]
OMIM gene
- Peripheral myelin protein 22 [OMIM gene]
Orphanet gene
- peripheral myelin protein 22 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- PMP22 Gene [NCIt concept]
- PMP22 gene [LOINC component]
- Peripheral myelin protein 22 [OMIM gene]

Keyword's position in hierarchy(ies) :

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