Glycogen Storage Disease Type 3

About the Disease
Glycogen Storage Disease Iii, also known as glycogen storage disease type iii, is related to atrial standstill 1 and hypertrophic cardiomyopathy. An important gene associated with Glycogen Storage Disease Iii is AGL (Amylo-Alpha-1, 6-Glucosidase, 4-Alpha-Glucanotransferase), and among its related pathways/superpathways are Metabolism and Disease. The drugs Famotidine and Cetirizine have been mentioned in the context of this disorder. Affiliated tissues include liver, heart and eye, and related phenotypes are short stature and intellectual disability, mild

Common Targets
AGL | SBDS

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Limb Girdle Muscular Dystrophy | Osteogenesis Imperfecta Type II | Arthritis, Gouty | Fanconi Anemia | Monilethrix | Congenital Heart Defects | Pain | Periventricular Nodular Heterotopia | T-cell Lymphoma, Subcutaneous Panniculitis-like | Adenocarcinoma | Oguchi Disease-2 | Stevens-Johnson Syndrome | Familial Pheochromocytoma-paraganglioma | Ileitis | Pseudoachondroplasia | Vitreoretinopathy, Proliferative | Arteriovenous Malformations | Familial Exudative Vitreoretinopathy | Cryopyrin-associated Periodic Syndromes | Infertility, Male | Myhre Syndrome | Otopalatodigital Syndrome Type 2 | Oligospermia | Coma | Wolfram Syndrome | Renal Hypouricemia | Dysgerminoma | Meningeal Melanocytoma | Dysmorphophobia | Raine Syndrome | Agranulocytosis | Epicondylitis | Bainbridge-Ropers Syndrome | Non-bullous Congenital Ichthyosiform Erythroderma | Glycogen Storage Disease Type 0, Muscle | Gilbert Syndrome | Bartter Syndrome | Muscular Dystrophy | Krabbe Disease | Chronic Lymphocytic Leukemia | 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