disease caused by disruption of disease has basis in disruption of glycogen metabolic process glycogen storage disease An inherited metabolic disorder characterized either by defects in glycogen synthesis or defects in the breaking down of glycogen. It results either in the creation of abnormal forms of glycogen or accumulation of glycogen in the tissues. COHD:434003 DOID:0050728 DOID:2747 GSD ICD10:E74.0 ICD10:E74.00 ICD9:271.0 MESH:D006008 MONDO:0002412 MedDRA:10061990 NCIT:C61272 Orphanet:79201 SCTID:29633007 UMLS:C0017919 glycogen metabolism disorder glycogen storage disease glycogen storage disorder glycogenoses glycogenosis inborn error of glycogen metabolic process inborn glycogen metabolic process disorder inborn glycogen storage disorder rare inborn error of glycogen metabolic process inborn errors of metabolism inborn carbohydrate metabolic disorder inborn disorder of energy metabolism