neuromedin B - CISMeF

Preferred Label : neuromedin B;

Approved symbol HGNC : NMB;

Alias symbols HGNC : MGC3936; MGC2277; MGC17211;

Chromosome HGNC : 15q25.2;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000197696;

Détails

Origin ID

HGNC:7842;

UMLS CUI

C1417740;

Automatic exact mappings (from CISMeF team)
- Neuromedin b [OMIM gene]
- Neuromedin-B [NCIt concept]
- neuromedin B [MeSH concept]
- neuromedin B [MeSH Supplementary Concept]
NCIt concept
- NMB Gene [NCIt concept]
OMIM gene
- Neuromedin b [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NMB Gene [NCIt concept]
- Neuromedin b [OMIM gene]

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

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients