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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Limb-girdle muscular dystrophy, type 2C


Other Names for this Disease
  • Adhalin deficiency, secondary
  • DMDA
  • DMDA1
  • Duchenne-like muscular dystrophy, autosomal recessive, type 1
  • Gamma-sarcoglycanopathy
More Names
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Tests & Diagnosis

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Testing

  • Orphanet lists international laboratories offering diagnostic testing for this condition. Click here and scroll down the page to learn more about the processes of certification, accreditation, and external quality assessment available to these labs. Click on Orphanet to view the list.