muscular dystrophy, congenital, 1B

Preferred Label : muscular dystrophy, congenital, 1B;

Origin ID

C565748;

UMLS CUI

C1858118;

Currated CISMeF NLP mapping
- Congenital muscular dystrophy type 1B [ICD-11 More detail]
- Congenital muscular dystrophy type 1B [ORDO Disease]
- Congenital muscular dystrophy type 1B (disorder) [SNOMED CT concept]
- Muscular dystrophy, congenital, 1b [OMIM Phenotype]
- congenital muscular dystrophy 1B [DO Concept]
MeSH term(s) associated for indexing
- muscular dystrophies [MeSH Descriptor]
Record concept(s)
- muscular dystrophy, congenital, 1B [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital muscular dystrophy type 1B [ORDO Disease]
- Congenital muscular dystrophy type 1B (disorder) [SNOMED CT concept]
- Muscular dystrophy, congenital, 1b [OMIM Phenotype]
- congenital muscular dystrophy 1B [DO Concept]