scapuloperoneal myopathy, X-Linked dominant

Preferred Label : scapuloperoneal myopathy, X-Linked dominant;

MeSH note : mutations in FHL1;

MeSH synonym : scapuloperoneal myopathy, FHL1-Related;

Details

Origin ID

C567481;

UMLS CUI

C2678061;

Currated CISMeF NLP mapping
- Scapuloperoneal myopathy, X-linked dominant [OMIM Phenotype]
- x linked dominant scapuloperoneal myopathy [Disease (Nov.)]
MeSH term(s) associated for indexing
- muscular dystrophy, emery-dreifuss [MeSH Descriptor]
Record concept(s)
- scapuloperoneal myopathy, X-Linked dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Scapuloperoneal myopathy, X-linked dominant [OMIM Phenotype]
- x linked dominant scapuloperoneal myopathy [Disease (Nov.)]

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