Disease phenotype	OMIM	Gene symbol (chromosome) protein
Giant axonal neuropathy-1	256850	GAN (16q24.1) gigaxonin
Gluatric aciduria IIc, included	231680	ETFDH (4q32-q35) electron-transferring-flavoprotein dehydrogenase
Glycogen branching enzyme deficiency	232500	GBE1 (3p12) glucan (1,4-alpha-), branching enzyme 1 (glycogen branching enzyme, Andersen disease, glycogen storage disease type IV)
Glycogen storage disease II	232300	GAA (17q25.2-q25.3) acid alpha-glucosidase preproprotein
Glycogen storage disease IIb	300257	LAMP2 (Xq24) lysosomal-associated membrane protein 2 precursor
glycogen storage disease type 0	611556	GYS1 (19q13.3) glycogen synthase 3 glycogen synthase 1 (muscle) glycogen synthase 1 (muscle)
Glycogen storage disease type IIIa	232400	AGL (1p21) Amylo-1,6-glucosidase, 4-alpha-glucanotransferase
Glycogen storage disease type IIIb	232400	AGL (1p21) Amylo-1,6-glucosidase, 4-alpha-glucanotransferase
Glycogen storage disease type IIIc	232400	AGL (1p21) Amylo-1,6-glucosidase, 4-alpha-glucanotransferase
Glycogen storage disease type IIId	232400	AGL (1p21) Amylo-1,6-glucosidase, 4-alpha-glucanotransferase
Glycogen storage disease VII	232800	PFKM (12q13.3) phosphofructokinase, muscle