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Autosomal dominant limb-girdle muscular dystrophy type 1D

Disease definition

Autosomal dominant limb-girdle muscular dystrophy type 1D (LGMD1D) is a limb girdle muscular dystrophy (LGMD ; see this term) characterized by muscular weakness, primarily affecting the pelvic and shoulder girdles with no bulbar weakness or dysarthria.

ORPHA:34516

  • Synonym(s):
    • LGMD1D
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal dominant 
  • Age of onset: Adult
  • ICD-10: G71.0
  • OMIM: 603511
  • UMLS: -
  • MeSH: -
  • GARD: 12528
  • MedDRA: -

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