MeSH Browser

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 Number: 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 MeSH Supplementary Concept Data 2024