lamin A/C - CISMeF

Preferred Label : lamin A/C;

Approved symbol HGNC : LMNA;

Name synonyms HGNC : progerin; mandibuloacral dysplasia type A;

Alias symbols HGNC : MADA; HGPS;

Chromosome HGNC : 1q22;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000160789;

Details

Origin ID

HGNC:6636;

UMLS CUI

C1416877;

Automatic exact mappings (from CISMeF team)
- Hutchinson-gilford progeria syndrome [OMIM Phenotype]
- Lamin C [FMA entity]
- Lamin a/C [OMIM gene]
- Lamin-A/C [NCIt concept]
- Mandibuloacral dysplasia with type a lipodystrophy [OMIM Phenotype]
- lamin A/C [ORDO Gene]
- lamin C [MeSH concept]
- lamin C [MeSH Supplementary Concept]
- lamin type a [MeSH Descriptor]
NCIt concept
- LMNA Gene [NCIt concept]
OMIM gene
- Lamin a/C [OMIM gene]
Orphanet gene
- lamin A/C [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- LMNA Gene [NCIt concept]
- LMNA gene [LOINC component]
- Lamin a/C [OMIM gene]

Keyword's position in hierarchy(ies) :

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