muscular dystrophy, congenital, type 1D

Preferred Label : muscular dystrophy, congenital, type 1D;

Origin ID

C563844;

UMLS CUI

C1837229;

Automatic exact mappings (from CISMeF team)
- muscular dystrophy-dystroglycanopathy type B6 [DO Concept]
Currated CISMeF NLP mapping
- Congenital muscular dystrophy type 1D [ORDO Disease]
- Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b, 6 [OMIM Phenotype]
MeSH term(s) associated for indexing
- brain [MeSH Descriptor]
- intellectual disability [MeSH Descriptor]
- muscular dystrophies [MeSH Descriptor]
Record concept(s)
- muscular dystrophy, congenital, type 1D [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital muscular dystrophy type 1D [ORDO Disease]
- Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b, 6 [OMIM Phenotype]