| 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.
|
Arteriohepatic dysplasia
|
Orphanet_52 |
|
|
AML M3
|
Orphanet_520 |
|
|
11p11.2 deletion
|
Orphanet_52022 |
|
|
Potocki-Shaffer syndrome
|
Orphanet_52022 |
|
|
Braddock syndrome
|
Orphanet_52047 |
|
|
Longman-Tolmie syndrome
|
Orphanet_52054 |
|
|
Graham-Cox syndrome
|
Orphanet_52055 |
|
|
Morava-Mehes syndrome
|
Orphanet_52056 |
|
|
Radiation-induced plexopathy
|
Orphanet_521123 |
|
|
Radiation-induced disorder
|
Orphanet_521132 |
|
|
Mirizzi syndrome
|
Orphanet_521219 |
|
|
Xq25 microtriplication
|
Orphanet_521258 |
|
|
SINO syndrome
|
Orphanet_521390 |
|
|
Dystonia-parkinsonism-hypermanganesemia syndrome
|
Orphanet_521406 |
|
|
ATP1A1-related CMT2
|
Orphanet_521414 |
|
