congenital disorder of glycosylation It (Q66299850)
Jump to navigation
Jump to search
human disease
- congenital disorder of glycosylation 1t
- glycogen storage disease type 14
- Congenital disorder of glycosylation type 1t
- Phosphoglucomutase-1 deficiency
- PGM1-CDG
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | congenital disorder of glycosylation It |
human disease |
|
Statements
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference