| 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.
|
Desbuquois syndrome
|
Orphanet_1425 |
|
|
Greenberg dysplasia
|
Orphanet_1426 |
|
|
HEM dysplasia
|
Orphanet_1426 |
|
|
Otospondylomegaepiphyseal dysplasia
|
Orphanet_1427 |
|
|
Parathyroid carcinoma
|
Orphanet_143 |
|
|
Paroxysmal choreoathetosis
|
Orphanet_1431 |
|
|
Paroxysmal dyskinesia
|
Orphanet_1431 |
|
|
Moloney syndrome
|
Orphanet_1433 |
|
|
Ayazi syndrome
|
Orphanet_1435 |
|
|
Monosomy Xq21
|
Orphanet_1435 |
|
|
Christian syndrome
|
Orphanet_1436 |
|
|
Ring 1
|
Orphanet_1437 |
|
|
r(1) syndrome
|
Orphanet_1437 |
|
|
Ring 10
|
Orphanet_1438 |
|
|
Ring 12
|
Orphanet_1439 |
|
