Disease phenotype
OMIM
Gene symbol (chromosome)
protein
protein
GBE1 (3p12)
glucan (1,4-alpha-), branching enzyme 1 (glycogen branching enzyme, Andersen disease, glycogen storage disease type IV)
Disease phenotype | OMIM | Gene symbol (chromosome) protein |
| Giant axonal neuropathy-1 (14.65) | ||
| Gluatric aciduria IIc, included (9.20, 9.24) | ||
| Glycogen branching enzyme deficiency (9.3) | GBE1 (3p12) glucan (1,4-alpha-), branching enzyme 1 (glycogen branching enzyme, Andersen disease, glycogen storage disease type IV) | |
| Glycogen storage disease II (9.1, 10.68) | ||
| Glycogen storage disease IIb (5.10) | ||
| glycogen storage disease of heart, lethal congenital (10.5, 9.10) | ||
| glycogen storage disease type 0 (9.9) | ||
| Glycogen storage disease type IIIa (9.2) | ||
| Glycogen storage disease type IIIb (9.2) | ||
| Glycogen storage disease type IIIc (9.2) | ||
| Glycogen storage disease type IIId (9.2) | ||
| Glycogen storage disease VII (9.5) | ||
| Glycogen storage disease X (9.12) | ||
| Glycogen storage disease XI (9.13) | ||
| Glycogen storage disease XIII (9.14) | ||
| Glycogen storage disease XIV (9.7) | ||
| Glycogen storage disease XV (9.8) | ||
| glycogen storage disease, type IXD (9.6) |