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Sarcoglycanopathy

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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

  • Mode of Inheritance

    VARIANTS

    80

    SEE THE VARIANTS →

    Genes

    External Links

    • OMIM
    • Orphanet

      207052

    • HPO
    • Medgen

      C2936331

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