| 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.
|
SPG31
|
Orphanet_101011 |
|
|
XHIGM
|
Orphanet_101088 |
|
|
Dentatorubropallidoluysian atrophy
|
Orphanet_101 |
|
|
Naito-Oyanagi disease
|
Orphanet_101 |
|
|
Troyer syndrome
|
Orphanet_101000 |
|
|
Mast syndrome
|
Orphanet_101001 |
|
|
Lison syndrome
|
Orphanet_101003 |
|
|
Romano-Ward syndrome
|
Orphanet_101016 |
|
|
TALDO deficiency
|
Orphanet_101028 |
|
|
Transaldolase deficiency
|
Orphanet_101028 |
|
|
Juberg-Hellman syndrome
|
Orphanet_101039 |
|
|
Familial hypofibrinogenemia
|
Orphanet_101041 |
|
|
Situs inversus
|
Orphanet_101063 |
|
|
Witschel dystrophy
|
Orphanet_101068 |
|
|
Cowchock syndrome
|
Orphanet_101078 |
|
