| 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.
|
Acquired peripheral movement disorder
|
Orphanet_221114 |
|
|
Aminopterin syndrome-like sine aminopterin
|
Orphanet_221120 |
|
|
Hydrocephaly/hydranencephaly due to cerebral vasculopathy
|
Orphanet_221126 |
|
|
Acrofrontofacionasal dysostosis type 2
|
Orphanet_2211 |
|
|
Acrofrontofacionasal syndrome type 2
|
Orphanet_2211 |
|
|
Encephaloclastic proliferative vasculopathy
|
Orphanet_221126 |
|
|
Combined immunodeficiency with facio-oculo-skeletal anomalies
|
Orphanet_221139 |
|
