Muscular dystrophy, limb-girdle, type 1A

Preferred Label : Muscular dystrophy, limb-girdle, type 1A;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0530367;

UMLS CUI

C1834659;

Automatic exact mappings (from CISMeF team)
- Myopathy, myofibrillar, 3 [OMIM Phenotype]
Currated CISMeF NLP mapping
- Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) [SNOMED CT concept]
- Muscular dystrophy, limb-girdle, type 1a [OMIM Phenotype]
- limb girdle muscular dystrophy type 1a [Disease (Nov.)]
Related record
- muscular dystrophy, limb-girdle, type 1A [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant limb-girdle muscular dystrophy type 1A [ORDO Disease]
- Muscular dystrophy, limb-girdle, type 1a [OMIM Phenotype]
- limb girdle muscular dystrophy type 1a [Disease (Nov.)]