256. Muscle glycogenosis Disease details / Clinical trials / Drug dev / DR info

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Clinical trials : 204 /  Drugs : 153 - (DrugBank : 29) / Drug target genes : 19 - Drug target pathways : 59

Other names	Muscular glycogenosis;Muscle glycogen storage disease;Muscular glycogen storage disease;
Disease group	Metabolic diseases
Domestic patients Med expenses recipients, FY2024 (corrected) (in Japanese)	30 patients Age distribution💬 256. Muscle glycogenosis × Age Num 0-9 - 10-19 - 20-29 8 30-39 1 40-49 9 50-59 3 60-69 4 70-74 2 75- 3
Clinical research form (in Japanese) MHLW Intractable Diseases, FY2026 (in Japanese)	Overview, diagnostic criteria, etc. (pdf), Clinical research form (pdf)
Specific pediatric chronic diseases, Japan (in Japanese)	-
Sub-diseases (Clinical research forms may not be available for all sub-diseases.)	No.	Name	Specific pediatric chronic diseases, Japan (in Japanese)
	256-1.	Glycogen storage disease type 0;GSD0;Glycogen synthase deficiency;	8-5-65. Glycogen synthase deficiency
	256-2.	Glycogen storage disease type II;GSDII;Pompe disease;Pompe syndrome;Alpha-1,4-glucosidase acid deficiency;	8-6-97. Pompe disease; glycogen storage disease type II
	256-3.	Glycogen storage disease type III;GSDIII;Cori disease;Cori syndrome;Forbes disease;Forbes syndrome;Glycogen debranching enzyme deficiency;	8-5-67. Glycogen storage disease type III
	256-4.	Glycogen storage disease type IV;GSDIV;Andersen disease;Glycogen-branching enzyme deficiency;GBED;	8-5-68. Glycogen storage disease type IV
	256-5.	Glycogen storage disease type V;GSDV;McArdle disease;Muscle phosphorylase deficiency;Muscular phosphorylase deficiency;	8-5-69. Glycogen storage disease type V
	256-6.	Glycogen storage disease type VII;GSDVII;Tarui disease;Tarui syndrome;Phosphofructokinase deficiency;PFK deficiency;	8-5-71. Glycogen storage disease type VII
	256-7.	Glycogen storage disease type IXd;GSDIXd;Phosphorylase kinase deficiency;	8-5-72. Glycogen storage disease type IX
	256-8.	Phosphoglycerate kinase deficiency;PGK deficiency;
	256-9.	Glycogen storage disease type X;GSDX;Phosphoglycerate mutase deficiency;
	256-10.	Glycogen storage diseass type XI;GSDXI;Kanno disease;Lactate dehydrogenase deficiency;
	256-11.	Glycogen storage diseass type XII;GSDXII;Aldolase A deficiency;
	256-12.	Glycogen storage diseass type XIII;GSDXIII;Beta-enolase deficiency;
	256-13.	Glycogen storage diseass type XIV;GSDXIV;Phosphoglucomutase deficiency;
	256-14.	Glycogen storage diseass type XV;GSDXV;Glycogenin 1 deficiency;