You are using an outdated browser. Please upgrade your browser to improve your experience.

myopathy, myosin storage, autosomal dominant

Disease Summary
Associated Targets (1)
Tclin

1


Uniprot Description A rare congenital myopathy characterized by subsarcolemmal hyalinized bodies in type 1 muscle fibers.
Mondo Term and Equivalent IDs
MONDO:0012018:  myopathy, myosin storage, autosomal dominant
MESH:C564253: 
SCTID:699267007: 
UMLS:C1842160: