| Disease Aliases (75) | Agl deficiency Agl glycogen storage disease Amylo-1,6-glucosidase deficiency Amylo 1,6 glucosidase deficiency Amylo-1,6-glucosidase deficiencies Cori disease Cori's disease Cori-forbes disease Coris disease Debrancher deficiencies Debrancher deficiencies, glycogen Debrancher deficiency Debrancher deficiency, glycogen Debrancher deficiency glycogen storage disease Debrancher enzyme deficiency Deficiencies, amylo-1,6-glucosidase Deficiencies, debrancher Deficiencies, glycogen debrancher Deficiency of 6-alpha-d-glucosidase Deficiency of amylo-1,6-glucosidase Deficiency of dextrin Deficiency, amylo-1,6-glucosidase Deficiency, debrancher Deficiency, glycogen debrancher Dextrinoses, limit Dextrinosis, limit Disease, cori Disease, cori's Disease, forbes Forbes disease Gbe deficiency, childhood combined hepatic and myopathic form Gde deficiency Glycogen debrancher deficiency Glycogen storage disease iiia Glycogen storage disease iiib Glycogen storage disease iiic Glycogen storage disease iiid Gsd iii Gsd iiia Gsd iiib Gsd iiic Gsd iiid Gsd due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form Gsd due to glycogen debranching enzyme deficiency Gsd type 3 Gsd type 4, childhood combined hepatic and myopathic form Gsd3 Gsdiii Gsdiv, childhood combined hepatic and myopathic form Glycogen debrancher deficiencies Glycogen debranching enzyme deficiency Glycogen storage disease iii Glycogen storage disease type 3 Glycogen storage disease type iii Glycogen storage disease type 4, childhood combined hepatic and myopathic form Glycogen storage disease type iv, childhood combined hepatic and myopathic form Glycogen storage disease, type iii Glycogen storage disease, type iii (disorder) Glycogenosis 3 Glycogenosis 3s Glycogenosis due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form Glycogenosis due to glycogen debranching enzyme deficiency Glycogenosis type 3 Glycogenosis type 4, childhood combined hepatic and myopathic form Glycogenosis type iii Glycogenosis type iv, childhood combined hepatic and myopathic form Limit dextrinosis Limit dextrinoses Limit dextrin - glycogen Deficiency of debranching enzyme Glycogen storage disease 3 Glycogen storage disease iii; gsd3 Glycogen storage disease caused by mutation in agl Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form Glycogen storage disease due to glycogen debranching enzyme deficiency |
Associated Genes (1) NCBI-RefSeq: AGL (Amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase) External Links: gnomAD browser Ensembl GeneCards
| |||||||
| Cross-references of Glycogen storage disease type III | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |