myopathy, congenital, with Fiber-Type disproportion, X-Linked

Preferred Label : myopathy, congenital, with Fiber-Type disproportion, X-Linked;

MeSH note : also known as CFTDX;

Origin ID

C567594;

UMLS CUI

C2749128;

Currated CISMeF NLP mapping
- Myopathy, congenital, with fiber-type disproportion, X-linked [OMIM Phenotype]
- X-linked congenital myopathy with fiber-type disproportion [DO Concept]
MeSH term(s) associated for indexing
- myopathies, structural, congenital [MeSH Descriptor]
Record concept(s)
- myopathy, congenital, with Fiber-Type disproportion, X-Linked [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Myopathy, congenital, with fiber-type disproportion, X-linked [OMIM Phenotype]