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Dimauro disease MeSH Supplementary Concept Data 2025


MeSH Supplementary
Dimauro disease
Unique ID
C536176
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C536176
Entry Term(s)
Deficiency Mutase Phosphoglycerate
Glycogen Storage Disease X
Gsd X
Gsd10
Human muscle phosphoglycerate mutase deficiency
Myopathy due to phosphoglycerate mutase deficiency
PGAMM deficiency
Pgam Deficiency
Phosphoglycerate Mutase Deficiency
Phosphoglycerate Mutase, Muscle, Deficiency of
Registry Numbers
0
Heading Mapped to
*Kidney Diseases
*Muscular Diseases
Phosphoglycerate Mutase / deficiency
Frequency
3
Date of Entry
2010/08/25
Revision Date
2013/10/24
Dimauro disease Preferred
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