has material basis in germline mutation in AGL disorder of glycogen metabolism glycogen storage disease III https://github.com/monarch-initiative/mondo/issues/4985 https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/glycogen_storage_disease_iii glycogen storage disease type 3 ICD10CM:E74.03 MEDGEN:6641 GSDIII glycogen storage disease III MONDO:0009291 Forbes disease GSD3 limit dextrinosis DOID:2748 UMLS:C0017922 Cori disease NANDO:1200826 Orphanet:366 glycogen storage disease caused by mutation in AGL glycogen storage disease type III AGL glycogen storage disease Cori-Forbes disease SCTID:66937008 GDE deficiency glycogenosis type III GARD:0009442 amylo-1,6-glucosidase deficiency MedDRA:10053250 Glycogen debranching enzyme (GDE) deficiency, or glycogen storage disease type 3 (GSD 3), is a form of glycogen storage disease characterized by severe muscle weakness and hepatopathy. MESH:D006010 GSD due to glycogen debranching enzyme deficiency glycogenosis type 3 OMIM:232400 GSD type 3 NANDO:1200844 NANDO:1201019 NANDO:2200539 glycogenosis due to glycogen debranching enzyme deficiency NCIT:C84736