Additional Disease Briefs

glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form

Also known as: GBE deficiency, non progressive hepatic form, GSD due to glycogen branching enzyme deficiency, non progressive hepatic form, GSD type 4, non progressive hepatic form, GSDIV, non progressive hepatic form, glycogen storage disease type 4, non progressive hepatic form, glycogen storage disease type IV, non progressive hepatic form, glycogenosis due to glycogen branching enzyme deficiency, non progressive hepatic form, glycogenosis type 4, non progressive hepatic form, glycogenosis type IV, non progressive hepatic form

glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form

Also known as: GBE deficiency, progressive hepatic form, GSD due to glycogen branching enzyme deficiency, progressive hepatic form, GSD type 4, progressive hepatic form, GSDIV, progressive hepatic form, glycogen storage disease type 4, progressive hepatic form, glycogen storage disease type IV, progressive hepatic form, glycogenosis due to glycogen branching enzyme deficiency, progressive hepatic form, glycogenosis type 4, progressive hepatic form, glycogenosis type IV, progressive hepatic form

glycogen storage disease due to lactate dehydrogenase H-subunit deficiency

Also known as: GSD due to lactate dehydrogenase H-subunit deficiency, LDH deficiency B, LDH-H subunit deficiency, LDHBD, glycogenosis due to lactate dehydrogenase H-subunit deficiency, lactate dehydrogenase B deficiency, lactate dehydrogenase deficiency type B, lactate dehydrogenase-B deficiency

glycogen storage disease due to lactate dehydrogenase M-subunit deficiency

Also known as: GSD 11, GSD XI, GSD due to lactate dehydrogenase M-subunit deficiency, GSD type 11, GSD11, LDH-M subunit deficiency, LDHA glycogen storage disease, glycogen storage disease XI, glycogen storage disease caused by mutation in LDHA, glycogen storage disease type 11, glycogenosis due to lactate dehydrogenase M-subunit deficiency, glycogenosis type 11, lactate dehydrogenase A deficiency, lactate dehydrogenase deficiency type A

glycogen storage disease due to liver phosphorylase kinase deficiency

glycogen storage disease due to muscle and heart glycogen synthase deficiency

Also known as: GSD 0B, GSD due to muscle and heart glycogen synthase deficiency, GSD type 0b, GSD0B, glycogen storage disease 0, muscle, glycogen storage disease due to glycogen synthase deficiency of heart, glycogen storage disease type 0, muscle, glycogen storage disease type 0b, glycogenosis due to muscle and heart glycogen synthase deficiency, glycogenosis type 0b, heart glycogen storage disease due to glycogen synthase deficiency, muscle glycogen storage disease 0, muscle glycogen synthase deficiency

glycogen storage disease due to muscle beta-enolase deficiency

Also known as: GSD 13, GSD due to muscle beta-enolase deficiency, GSD13, GSDXIII, enolase 3 deficiency, enolase-Beta deficiency, glycogen storage disease 13, glycogen storage disease XIII, glycogen storage disease due to muscle beta-enolase deficiency, glycogen storage disease type 13, glycogenosis due to muscle beta-enolase deficiency, glycogenosis type 13, muscle enolase deficiency, muscular enolase deficiency

glycogen storage disease due to phosphoglycerate mutase deficiency

Also known as: GSD 10, GSD due to phosphoglycerate mutase deficiency, GSD type 10, GSD10, GSDX, PGAM deficiency, PGAM2 glycogen storage disease, PGAMM deficiency, Phosphoglycerate mutase deficiency, Phosphoglycerate mutase, muscle, deficiency of, glycogen storage disease 10, glycogen storage disease X, glycogen storage disease caused by mutation in PGAM2, glycogen storage disease type 10, glycogenosis due to phosphoglycerate mutase deficiency, muscle phosphoglycerate mutase deficiency, myopathy due to Phosphoglycerate mutase deficiency, myopathy due to phosphoglycerate mutase deficiency