muscular dystrophy, congenital, due to partial LAMA2 deficiency

Preferred Label : muscular dystrophy, congenital, due to partial LAMA2 deficiency;

MeSH note : mutation in laminin alpha-2 (LAMA2);

Origin ID

C564317;

UMLS CUI

C1842898;

Automatic exact mappings (from CISMeF team)
- Muscular dystrophy, congenital merosin-deficient, 1a [OMIM Phenotype]
MeSH term(s) associated for indexing
- muscular dystrophies [MeSH Descriptor]
Record concept(s)
- muscular dystrophy, congenital, due to partial LAMA2 deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]