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

sarcoglycanopathy

Disease Summary
Associated Targets (4)
Tbio

4


Mondo Description Deficiencies or mutations in the genes for the sarcoglycan complex subunits. A variety of phenotypes are associated with these mutations including a subgroup of autosomal recessive limb girdle muscular dystrophies, cardiomyopathies, and respiratory deficiency.
Mondo Term and Equivalent IDs
MONDO:0016140:  sarcoglycanopathy
MESH:D058088: 
Orphanet:207052: