| 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.
|
Neovascular glaucoma
|
Orphanet_94058 |
|
|
Uremic pruritus
|
Orphanet_94059 |
|
|
Deletion 12q14
|
Orphanet_94063 |
|
|
Monosomy 12q14
|
Orphanet_94063 |
|
|
Deafness-infertility syndrome
|
Orphanet_94064 |
|
|
Monosomy 15q24
|
Orphanet_94065 |
|
|
Spranger-Wiedemann disease
|
Orphanet_94068 |
|
|
Autoimmune enteropathy
|
Orphanet_94075 |
|
|
Non-functioning paraganglioma
|
Orphanet_94080 |
|
|
Non-secreting paraganglioma
|
Orphanet_94080 |
|
|
Partington syndrome
|
Orphanet_94083 |
|
|
Partington-Mulley syndrome
|
Orphanet_94083 |
|
|
Drummond syndrome
|
Orphanet_94086 |
|
|
Mills syndrome
|
Orphanet_94091 |
|
|
D-glyceric acidemia
|
Orphanet_941 |
|
