All diseases

OMIM ID
261670
OMIM term:
GLYCOGEN STORAGE DISEASE X; GSD10
Alternative terms:
GSD X
PHOSPHOGLYCERATE MUTASE, MUSCLE, DEFICIENCY OF
MYOPATHY DUE TO PHOSPHOGLYCERATE MUTASE DEFICIENCY
PGAMM DEFICIENCY
(∗) Location:
7p13  
(†) Associated OMIM genes:
PGAM2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/3uaw1czg