/glycogen storage disease III

glycogen storage disease III

Rare Disease

MONDO:0009291

Also Known As

AGL glycogen storage diseaseCori diseaseCori-Forbes diseaseForbes diseaseGDE deficiencyGSD due to glycogen debranching enzyme deficiencyGSD type 3GSDIIIamylo 1,6 glucosidase deficiencyamylo-1,6-glucosidase deficiencydeficiency of debranching enzymedeficiency of dextringlycogen storage disease IIIglycogen storage disease caused by mutation in AGLglycogen storage disease type 3glycogen storage disease type IIIglycogen storage disease, type IIIglycogenosis due to glycogen debranching enzyme deficiencyglycogenosis type 3glycogenosis type IIIlimit dextrinosisAgl deficiencyGSD3Gde deficiencyglycogen Debrancher deficiencyglycogen storage disease 3glycogen storage disease IIICglycogen storage disease IIIDglycogen storage disease IIIaglycogen storage disease IIIbglycogen storage disease due to glycogen debranching enzyme deficiency

Definition

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.