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| Predicate | Object |
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| rdf:type | |
| calbc:hasCorrelation | |
| skos:exactMatch | |
| skos:definition |
MSH: 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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| skos:inScheme | |
| skos-xl:prefLabel | |
| skos-xl:altLabel |