muscular dystrophy, limb-girdle, type 1A

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

MeSH synonym : muscular dystrophy, proximal, type 1A; muscular dystrophy, Limb-Girdle, Type1A;

Détails

Origin ID

C535906;

UMLS CUI

C1834659;

CISMeF manual mappings
- Autosomal dominant limb-girdle muscular dystrophy type 1A [ORDO Disease]
Currated CISMeF NLP mapping
- Autosomal dominant limb girdle muscular dystrophy type 1A (disorder) [SNOMED CT concept]
- Limb-girdle muscular dystrophy 1A, myotilin myopathy [ICD-11 More detail]
- Muscular dystrophy, limb-girdle, type 1a [OMIM Phenotype]
- autosomal dominant limb-girdle muscular dystrophy type 1A [DO Concept]
- limb girdle muscular dystrophy type 1a [Disease (Nov.)]
MeSH term(s) associated for indexing
- muscular dystrophies, limb-girdle [MeSH Descriptor]
Record concept(s)
- Muscular dystrophy, limb-girdle, type 1A [MeSH 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.)]

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