disease disrupts disease causes disruption of disease has feature glucose-6-phosphatase activity Hepatomegaly disorder of glycogen metabolism glycogen storage disease I https://www.malacards.org/card/glycogen_storage_disease_ia NCIT:C84733 glycogenosis type 1 NORD:1193 glycogen storage disease I hepatorenal glycogenosis MONDO:0002413 Glycogenosis due to glucose-6-phosphatase (G6P) deficiency or glycogen storage disease, (GSD), type 1, is a group of inherited metabolic diseases, including types a and b, and characterized by poor tolerance to fasting, growth retardation and hepatomegaly resulting from accumulation of glycogen and fat in the liver. glycogen storage disease due to glucose-6-phosphatase deficiency GSD type I GARD:0016523 MESH:D005953 von Gierke disease DOID:0081329 MONDO:0018220 GSD type 1 NANDO:1201018 NANDO:1200840 glycogen storage disease type 1 Glycogen Storage Disease Type I von Gierke's disease glycogen storage disease due to G6P deficiency NANDO:2200538 GSD due to G6P deficiency glycogen storage disease type I Orphanet:364 G6P deficiency GSD1 ICD10CM:E74.01 glycogenosis type I MedDRA:10018464 MEDGEN:6640 glycogen storage disease, type I UMLS:C0017920 SCTID:7265005 obsolete nephropathy secondary to a storage or other metabolic disease