muscular dystrophy, Limb-Girdle, type 1F

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

MeSH synonym : LGMD1F;

Origin ID

C564242;

UMLS CUI

C1842062;

Currated CISMeF NLP mapping
- Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) [SNOMED CT concept]
- Muscular dystrophy, limb-girdle, autosomal dominant 2 [OMIM Phenotype]
- TNP03-related limb-girdle muscular dystrophy D2 [ORDO Disease]
- autosomal dominant limb-girdle muscular dystrophy type 2 [DO Concept]
- limb girdle muscular dystrophy type 1f [Disease (Nov.)]
MeSH term(s) associated for indexing
- muscular dystrophies, limb-girdle [MeSH Descriptor]
Record concept(s)
- muscular dystrophy, Limb-Girdle, type 1F [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant limb girdle muscular dystrophy type 1F (disorder) [SNOMED CT concept]
- Muscular dystrophy, limb-girdle, autosomal dominant 2 [OMIM Phenotype]
- TNP03-related limb-girdle muscular dystrophy D2 [ORDO Disease]