myopathy, myofibrillar, Bag3-Related

Preferred Label : myopathy, myofibrillar, Bag3-Related;

MeSH note : mutation in BAG3;

Origin ID

C567843;

UMLS CUI

C2751831;

Currated CISMeF NLP mapping
- Myopathy, myofibrillar, 6 [OMIM Phenotype]
- myofibrillar myopathy 6 [DO Concept]
MeSH term(s) associated for indexing
- myopathies, structural, congenital [MeSH Descriptor]
Record concept(s)
- myopathy, myofibrillar, Bag3-Related [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Muscular dystrophy, Selcen type [ORDO Disease]
- Myopathy, myofibrillar, 6 [OMIM Phenotype]
- myofibrillar myopathy 6 [DO Concept]