limb-girdle muscular dystrophy, type 1B

Preferred Label : limb-girdle muscular dystrophy, type 1B;

MeSH synonym : muscular dystrophy, proximal, type 1B; LGMD1B; muscular dystrophy, Limb-Girdle, type 1B;

Details

Origin ID

C535898;

UMLS CUI

C1834653;

CISMeF manual mappings
- Autosomal dominant limb-girdle muscular dystrophy type 1B [ORDO Disease]
Currated CISMeF NLP mapping
- Autosomal dominant limb girdle muscular dystrophy type 1B (disorder) [SNOMED CT concept]
- Muscular dystrophy, limb-girdle, type 1b [OMIM Phenotype]
- autosomal dominant limb-girdle muscular dystrophy type 1B [DO Concept]
- limb girdle muscular dystrophy type 1b [Disease (Nov.)]
MeSH term(s) associated for indexing
- muscular dystrophies, limb-girdle [MeSH Descriptor]
Record concept(s)
- Limb-girdle muscular dystrophy, type 1B [MeSH concept]
See also (suggested by CISMeF)
- lamins [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant limb-girdle muscular dystrophy type 1B [ORDO Disease]
- Muscular dystrophy, limb-girdle, type 1b [OMIM Phenotype]

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