Myelin protein zero

Preferred Label : Myelin protein zero;

Symbol : MPZ;

CISMeF acronym : MPZ;

Type : Gene;

Alternative titles and symbols : Myelin glycoprotein p-zero; Myelin protein, peripheral; P0; MPP;

Ensembl ID : ENSG00000158887;

Prefixed ID : *159440;

Détails

Origin ID

159440;

UMLS CUI

C1417248;

Automatic exact mappings (from CISMeF team)
- MPZ gene [LOINC component]
- Multipotent Bone Marrow Stem Cell [NCIt concept]
- Peripheral myelin protein (substance) [SNOMED CT concept]
- RPLP0 wt Allele [NCIt concept]
- myelin P0 protein [MeSH Descriptor]
- myelin protein zero [ORDO Gene]
- myelin protein zero [HGNC gene]
- peripheral myelin protein [SNOMED Notion]
HGNC gene
- myelin protein zero [HGNC gene]
NCIt concept(s)
- MPZ Gene [NCIt concept]
- MPZ wt Allele [NCIt concept]
- Myelin Protein P0 [NCIt concept]
ORDO concept(s)
- myelin protein zero [ORDO Gene]
Phenotypes related
- Charcot-marie-tooth Disease, Dominant intermediate D [OMIM Phenotype]
- Charcot-marie-tooth disease, axonal, type 2i [OMIM Phenotype]
- Charcot-marie-tooth disease, axonal, type 2j [OMIM Phenotype]
- Charcot-marie-tooth disease, demyelinating, type 1b [OMIM Phenotype]
- Hypertrophic neuropathy of dejerine-sottas [OMIM Phenotype]
- Neuropathy, congenital hypomyelinating, 2 [OMIM Phenotype]
- Roussy-levy hereditary areflexic dystasia [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MPZ Gene [NCIt concept]
- MPZ gene [LOINC component]
- myelin protein zero [HGNC gene]

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