Lamin b2 - CISMeF

Preferred Label : Lamin b2;

Symbol : LMNB2;

CISMeF acronym : LMNB2;

Type : Gene;

Ensembl ID : ENSG00000176619;

Prefixed ID : *150341;

Details

Origin ID

150341;

UMLS CUI

C1416878;

Automatic exact mappings (from CISMeF team)
- lamin B2 [ORDO Gene]
- lamin B2 [HGNC gene]
- lamin B2 [MeSH Supplementary Concept]
- lamin B2 [MeSH concept]
HGNC gene
- lamin B2 [HGNC gene]
ORDO concept(s)
- lamin B2 [ORDO Gene]
Phenotypes related
- Epilepsy, progressive myoclonic, 9 [OMIM Phenotype]
- Lipodystrophy, partial, acquired, susceptibility to [OMIM Phenotype]
- Microcephaly 27, primary, autosomal dominant [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- lamin B2 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients