nebulin - CISMeF

Preferred Label : nebulin;

Approved symbol HGNC : NEB;

Name synonyms HGNC : nemaline myopathy type 2;

Alias symbols HGNC : NEB177D;

Chromosome HGNC : 2q23.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000183091;

Détails

Origin ID

HGNC:7720;

UMLS CUI

C1417656;

Automatic exact mappings (from CISMeF team)
- Nebulin [OMIM gene]
- Nebulin [FMA entity]
- nebulin [ORDO Gene]
- nebulin [MeSH Supplementary Concept]
- nebulin [MeSH concept]
NCIt concept
- NEB Gene [NCIt concept]
OMIM gene
- Nebulin [OMIM gene]
Orphanet gene
- nebulin [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NEB Gene [NCIt concept]
- NEB gene [LOINC component]
- Nebulin [OMIM gene]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients