| 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.
|
DYT12
|
Orphanet_71517 |
|
|
CAR syndrome
|
Orphanet_71505 |
|
|
Cancer-associated retinopathy
|
Orphanet_71505 |
|
|
Paraneoplastic retinopathy
|
Orphanet_71505 |
|
|
Dystonia 12
|
Orphanet_71517 |
|
|
Rapid-onset dystonia-parkinsonism
|
Orphanet_71517 |
|
|
Psychogenic dystonia
|
Orphanet_71519 |
|
|
POMC deficiency
|
Orphanet_71526 |
|
|
PCI deficiency
|
Orphanet_71528 |
|
|
MC4R deficiency
|
Orphanet_71529 |
|
|
GSD type 9D
|
Orphanet_715 |
|
|
Glycogenosis type 9D
|
Orphanet_715 |
|
|
GSD type 9E
|
Orphanet_715 |
|
|
Glycogenosis type 9E
|
Orphanet_715 |
|
|
GSD type IXd
|
Orphanet_715 |
|
