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congenital structural myopathy

Disease Summary
Associated Targets (134)
Tbio

81

Tclin

31

Tchem

19

Tdark

3


Mondo Description A group of rare genetic muscle disorders characterized by hypotonia, muscle weakness, and delayed development of motor skills.
Mondo Term and Equivalent IDs
MONDO:0002921:  congenital structural myopathy
MESH:D020914: 
NCIT:C84648: 
UMLS:C0752282: