myelin protein zero

Preferred Label : myelin protein zero;

Approved symbol HGNC : MPZ;

Alias symbols HGNC : P0; CMT2I; CMT2J; HMSNIB;

Chromosome HGNC : 1q23.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000158887;

Details

Origin ID

HGNC:7225;

UMLS CUI

C1417248;

Automatic exact mappings (from CISMeF team)
- Charcot-marie-tooth disease, axonal, type 2i [OMIM Phenotype]
- Charcot-marie-tooth disease, axonal, type 2j [OMIM Phenotype]
- Myelin protein zero [OMIM gene]
- myelin P0 protein [MeSH Descriptor]
- myelin protein zero [ORDO Gene]
NCIt concept
- MPZ Gene [NCIt concept]
OMIM gene
- Myelin protein zero [OMIM gene]
Orphanet gene
- myelin protein zero [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MPZ Gene [NCIt concept]
- MPZ gene [LOINC component]
- Myelin protein zero [OMIM gene]

Keyword's position in hierarchy(ies) :

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