Emerin - CISMeF

Preferred Label : Emerin;

Symbol : EMD;

CISMeF acronym : EMD;

Type : Gene;

Alternative titles and symbols : STA;

Ensembl ID : ENSG00000102119;

Prefixed ID : *300384;

Details

Origin ID

300384;

UMLS CUI

C1414386;

Automatic exact mappings (from CISMeF team)
- Electromechanical Dissociation by ECG Finding [NCIt concept]
- Electromechanical dissociation (disorder) [SNOMED CT concept]
- Extramedullary Disease in Multiple Myeloma [NCIt concept]
- emerin [ORDO Gene]
- emerin [MeSH Supplementary Concept]
- emerin [HGNC gene]
- emerin [MeSH concept]
HGNC gene
- emerin [HGNC gene]
NCIt concept(s)
- EMD Gene [NCIt concept]
- EMD wt Allele [NCIt concept]
- Emerin [NCIt concept]
ORDO concept(s)
- emerin [ORDO Gene]
Phenotypes related
- Emery-dreifuss muscular dystrophy 1, X-linked [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- emerin [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients