Laminin, alpha-2

Preferred Label : Laminin, alpha-2;

Symbol : LAMA2;

CISMeF acronym : LAMA2;

Type : Gene;

Alternative titles and symbols : Laminin 2, heavy chain;

Included titles and symbols : Merosin; Laminin 2; Laminin M; LAMM;

Ensembl ID : ENSG00000196569;

Prefixed ID : *156225;

Details

Origin ID

156225;

UMLS CUI

C1416776;

Automatic exact mappings (from CISMeF team)
- LAMA2 gene [LOINC component]
- laminin [MeSH Descriptor]
- laminin M [MeSH concept]
- laminin subunit alpha 2 [ORDO Gene]
- laminin subunit alpha 2 [HGNC gene]
- merosin [MeSH concept]
HGNC gene
- laminin subunit alpha 2 [HGNC gene]
NCIt concept(s)
- LAMA2 Gene [NCIt concept]
- LAMA2 wt Allele [NCIt concept]
- Laminin Subunit Alpha-2 [NCIt concept]
ORDO concept(s)
- laminin subunit alpha 2 [ORDO Gene]
Phenotypes related
- Muscular dystrophy, congenital merosin-deficient, 1a [OMIM Phenotype]
- Muscular dystrophy, limb-girdle, autosomal recessive 23 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- LAMA2 gene [LOINC component]
- laminin subunit alpha 2 [HGNC gene]

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