| Disease Aliases (30) | 1,4,alpha-glucan 6-alpha-glucosyltransferase deficiency Amylopectinosis Andersen disease Andersen disease (gsd iv) Andersen's disease Brancher deficiency Brancher deficiency glycogen storage disease Brancher deficiency glycogenosis Branching enzyme deficiency Branching-transferase deficiency glycogenosis Cirrhosis, familial, with deposition of abnormal glycogen Deficiency of 1,4-alpha-glucan branching enzyme Deficiency of amylo-(1,4,6)-transglycosylase Deficiency of branching enzyme Gbe1 deficiency Gbe1 glycogen storage disease Glycogen branching enzyme deficiency Glycogen storage disease caused by mutation in gbe1 Glycogen storage disease due to glycogen branching enzyme deficiency Glycogen storage disease type 4 Glycogen storage disease, type 4 Glycogenosis due to glycogen branching enzyme deficiency Glycogenosis iv Glycogenosis type 4 Glycogenosis type iv Glycogenosis, type 4 Gsd due to glycogen branching enzyme deficiency Gsd iv Gsd type 4 Gsd type iv |
Associated Genes (0) | |||||||
| Cross-references of Glycogen storage disease, type IV | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |