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Dimauro disease [Supplementary Concept]

Date introduced: August 25, 2010

MeSH Unique ID: C536176

Heading Mapped to:

Entry Terms:

  • Human muscle phosphoglycerate mutase deficiency
  • Myopathy due to phosphoglycerate mutase deficiency
  • PGAMM deficiency
  • Pgam Deficiency
  • Phosphoglycerate Mutase Deficiency
  • Deficiency Mutase Phosphoglycerate
  • Gsd X
  • Gsd10
  • Glycogen Storage Disease X
  • Phosphoglycerate Mutase, Muscle, Deficiency of

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