Lamin b1 - CISMeF

Preferred Label : Lamin b1;

Symbol : LMNB1;

CISMeF acronym : LMNB1;

Type : Gene;

Alternative titles and symbols : LMNB;

Ensembl ID : ENSG00000113368;

Prefixed ID : *150340;

Details

Origin ID

150340;

UMLS CUI

C1334345;

Automatic exact mappings (from CISMeF team)
- LMNB1 Gene [NCIt concept]
- LMNB1 wt Allele [NCIt concept]
- Lamin-B1 [NCIt concept]
- lamin B1 [ORDO Gene]
- lamin B1 [HGNC gene]
- lamin B1 [MeSH concept]
- lamin B1 [MeSH Supplementary Concept]
HGNC gene
- lamin B1 [HGNC gene]
NCIt concept(s)
- LMNB1 Gene [NCIt concept]
- LMNB1 wt Allele [NCIt concept]
- Lamin-B1 [NCIt concept]
ORDO concept(s)
- lamin B1 [ORDO Gene]
Phenotypes related
- Leukodystrophy, demyelinating, adult-onset, autosomal dominant [OMIM Phenotype]
- Microcephaly 26, primary, autosomal dominant [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- LMNB1 Gene [NCIt concept]
- lamin B1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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