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.
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qualitative or quantitative defects of alpha-sarcoglycan
MONDO:0016141
qualitative or quantitative defects of beta-sarcoglycan
MONDO:0016142
qualitative or quantitative defects of gamma-sarcoglycan
MONDO:0016143
qualitative or quantitative defects of delta-sarcoglycan
MONDO:0016144
neuromuscular disease caused by qualitative or quantitative defects of dysferlin
MONDO:0016145
caveolinopathy
MONDO:0016146