disease caused by disruption of disease has basis in disruption of glucose-6-phosphate transmembrane transporter activity glycogen storage disease due to glucose-6-phosphatase deficiency type IB Editor note: TODO decide whether to merge Ic G6P deficiency type IB G6P translocase deficiency G6PT deficiency GARD:0002515 GSD Ib GSD Ic GSD due to G6P deficiency type IB GSD due to G6PT deficiency GSD type 1 non a GSD type 1b GSD type IB GSD1B GSD1C GSDIb Glycogenosis due to glucose-6-phosphatase deficiency (G6P) type b, or glycogen storage disease (GSD) type 1b, is a type of glycogenosis due to G6P deficiency. Gsd1C ICD10:E74.0 MESH:C562594 MONDO:0009288 NCIT:C122661 OMIM:232220 OMIM:232240 Orphanet:79259 SCTID:237965005 SCTID:30102006 UMLS:C0342749 glucose-6-phosphate Transport defect glycogen storage disease Ib glycogen storage disease Ic glycogen storage disease Id glycogen storage disease due to G6P deficiency type IB glycogen storage disease type 1b glycogen storage disease type I non-a glycogen storage disease type IB glycogen storage disease type Ic glycogenosis due to glucose-6-phosphatase deficiency type 1b glycogenosis due to glucose-6-phosphatase transport defect type IB glycogenosis type 1b glycogenosis type IB constitutional neutropenia glycogen storage disease type 1 due to SLC37A4 mutation disease of transporter activity