| manager |
|
| language |
- |
| license |
- |
| created at |
2024-09-23 16:23:50 UTC |
| updated at |
2024-09-23 18:22:39 UTC |
|
Terms for rare diseases as defined in ORDO.
The entries were initially sourced from the ORDO version 2024-07-03 as stored in BioPortal.
Namespace: http://www.orpha.net/ORDO/
|
20,514 entries
|
There is 0 pattern entry.
|
ALG9-CDG
|
Orphanet_79328 |
|
|
CDG-IL
|
Orphanet_79328 |
|
|
CDG1L
|
Orphanet_79328 |
|
|
Mannosyltransferase 7-9 deficiency
|
Orphanet_79328 |
|
|
Carbohydrate deficient glycoprotein syndrome type IL
|
Orphanet_79328 |
|
|
Congenital disorder of glycosylation type 1L
|
Orphanet_79328 |
|
|
CDG syndrome type IL
|
Orphanet_79328 |
|
