Limb-Girdle muscular dystrophy, type 1G

Preferred Label : Limb-Girdle muscular dystrophy, type 1G;

MeSH synonym : LGMD1G;

Origin ID

C563794;

UMLS CUI

C1836765;

Currated CISMeF NLP mapping
- Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) [SNOMED CT concept]
- HNRNPDL-related limb-girdle muscular dystrophy D3 [ORDO Disease]
- Muscular dystrophy, limb-girdle, autosomal dominant 3 [OMIM Phenotype]
- autosomal dominant limb-girdle muscular dystrophy type 3 [DO Concept]
- limb girdle muscular dystrophy type 1g [Disease (Nov.)]
MeSH term(s) associated for indexing
- muscular dystrophies, limb-girdle [MeSH Descriptor]
Record concept(s)
- Limb-Girdle muscular dystrophy, type 1G [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant limb girdle muscular dystrophy type 1G (disorder) [SNOMED CT concept]
- HNRNPDL-related limb-girdle muscular dystrophy D3 [ORDO Disease]
- Muscular dystrophy, limb-girdle, autosomal dominant 3 [OMIM Phenotype]