laminin subunit alpha 2

Preferred Label : laminin subunit alpha 2;

Approved symbol HGNC : LAMA2;

Name synonyms HGNC : congenital muscular dystrophy; merosin;

Chromosome HGNC : 6q22.33;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000196569;

Details

Origin ID

HGNC:6482;

UMLS CUI

C1416776;

Automatic exact mappings (from CISMeF team)
- Congenital muscular dystrophy [ORDO Disease]
- Congenital muscular dystrophy [ICD-11 Subcategory]
- Congenital muscular dystrophy [HPO term]
- Laminin, alpha-2 [OMIM gene]
- congenital muscular dystrophy [DO Concept]
- laminin [MeSH Descriptor]
- laminin subunit alpha 2 [ORDO Gene]
- merosin [MeSH concept]
NCIt concept
- LAMA2 Gene [NCIt concept]
OMIM gene
- Laminin, alpha-2 [OMIM gene]
Orphanet gene
- laminin subunit alpha 2 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- LAMA2 gene [LOINC component]
- Laminin, alpha-2 [OMIM gene]

Keyword's position in hierarchy(ies) :

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