muscular dystrophy, Limb-Girdle, type 1C

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

MeSH note : mutation in CAV3;

MeSH synonym : LGMD1C;

Origin ID

C563362;

UMLS CUI

C1832567;

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