disease has basis in disruption of disease caused by disruption of glucose-6-phosphate transmembrane transporter activity glycogen storage disease Ib https://github.com/monarch-initiative/mondo/issues/430 https://github.com/monarch-initiative/mondo/issues/4985 https://www.malacards.org/card/glycogen_storage_disease_due_to_glucose_6_phosphatase_deficiency_type_ib https://www.malacards.org/card/glycogen_storage_disease_ib https://www.malacards.org/card/glycogen_storage_disease_ic MONDO:0009288 glycogen storage disease type Ic NANDO:1200841 NANDO:2200754 glycogenosis type 1b glycogen storage disease Ic glycogen storage disease Ib G6PT deficiency NANDO:2201154 MESH:C562594 GSD type IB GSD type 1 non a glycogen storage disease type 1b NCIT:C122661 Type Ic was merged with Ib because they involve the same gene. G6P deficiency type IB Orphanet:79259 OMIM:232240 glycogen storage disease due to G6P deficiency type IB G6P translocase deficiency GSD due to G6PT deficiency SCTID:237965005 GSD1C glycogenosis type IB DOID:0081330 A type of glycogenosis due to G6P deficiency. MEDGEN:78644 DOID:0081331 GSD Ib glucose-6-phosphate transport defect GARD:0002515 glycogen storage disease type IB GSD due to G6P deficiency type IB SCTID:30102006 GSD type 1b glycogenosis due to glucose-6-phosphatase deficiency type 1B UMLS:C0268146 GSD1B glycogenosis due to glucose-6-phosphatase transport defect type IB GSDIb glycogen storage disease type I non-a OMIM:232220 constitutional neutropenia glycogen storage disease type 1 due to SLC37A4 mutation