myopathy, hyaline body, autosomal recessive

Preferred Label : myopathy, hyaline body, autosomal recessive;

Origin ID

C564970;

UMLS CUI

C1850709;

Currated CISMeF NLP mapping
- Congenital myopathy 7b, myosin storage, autosomal recessive [OMIM Phenotype]
- Hyaline body myopathy [ICD-11 More detail]
- Myosin storage myopathy [ORDO Disease]
MeSH term(s) associated for indexing
- muscular diseases [MeSH Descriptor]
Record concept(s)
- myopathy, hyaline body, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital myopathy 7b, myosin storage, autosomal recessive [OMIM Phenotype]
- Hyaline body myopathy [ICD-11 More detail]
- Myosin storage myopathy [ORDO Disease]