Congenital disorder of glycosylation
Congenital disorder of glycosylation type Ia (CDG-Ia), also known as phosphomannomutase 2 deficiency, is an inherited condition that affects many parts of the body.
Associated Genes
| Gene Name | Chromosome number | BMRB Entries | PDB Entries |
|---|---|---|---|
| RFT1 | 3 | ||
| MPI | 15 | ||
| COG7 | 16 | ||
| ALG1 | 16 | ||
| PMM2 | 16 | PDB Entries | |
| PMM1 | 22 | PDB Entries |