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Diseases

Genetic and Rare Diseases Information Center (GARD)

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Limb-girdle muscular dystrophy, type 2C


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Other Names for Limb-girdle muscular dystrophy, type 2C

  • Adhalin deficiency, secondary
  • Autosomal recessive limb-girdle muscular dystrophy type 2C
  • DMDA
  • DMDA1
  • Duchenne-like muscular dystrophy, autosomal recessive, type 1
  • Epileptic encephalopathy with global cerebral demyelination
  • Familial primary localized cutaneous amyloidosis
  • FPLCA
  • Gamma-sarcoglycanopathy
  • LGMD
  • LGMD2C
  • Limb-girdle muscular dystrophy
  • Limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency
  • Limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency
  • Maghrebian myopathy
  • Mitochondrial aspartate-glutamate carrier 1 deficiency
  • Muscular dystrophy, Duchenne-like
  • Severe childhood autosomal recessive muscular dystrophy, North African type
See Disclaimer regarding information on this site. Some links on this page may take you to organizations outside of the National Institutes of Health.