| CUI | Disease | Vocabulary | Name in Vocabulary | Code |
|---|---|---|---|---|
| C1856301 | GSD IV, Classic Hepatic | DO | glycogen storage disease IV | 2750 |
| C1856301 | GSD IV, Classic Hepatic | MONDO | glycogen storage disease due to glycogen branching enzyme deficiency | 0009292 |
| C1856301 | GSD IV, Classic Hepatic | MSH | GSD IV, Classic Hepatic | C565539 |
| C1856301 | GSD IV, Classic Hepatic | OMIM | GLYCOGEN STORAGE DISEASE IV | 232500 |
| C1856301 | GSD IV, Classic Hepatic | OMIM | AMYLOPECTINOSIS | 232500 |
| C1856301 | GSD IV, Classic Hepatic | OMIM | GSD IV, CLASSIC HEPATIC | 232500 |
| C1856301 | GSD IV, Classic Hepatic | OMIM | GSD IV, NEUROMUSCULAR FORM, FATAL PERINATAL | 232500 |
| C1856301 | GSD IV, Classic Hepatic | OMIM | GSD IV, NEUROMUSCULAR FORM, CONGENITAL | 232500 |
| C1856301 | GSD IV, Classic Hepatic | OMIM | GSD IV, NEUROMUSCULAR FORM, CHILDHOOD | 232500 |