Disease #04229 (CDG2 (glycosylation, congenital disorder of, type II (CDG-2)))
| Official abbreviation |
CDG2 |
| Name |
glycosylation, congenital disorder of, type II (CDG-2) |
| OMIM ID |
- |
| Inheritance |
- |
| Individuals reported having this disease |
9 |
| Phenotype entries for this disease |
9 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-03-20 21:54:25 +01:00 (CET) |
| Date last edited |
2021-12-11 13:56:28 +01:00 (CET) |
Individuals
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