| 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.
|
Rare parathyroid disease and phosphocalcic metabolism anomaly
|
Orphanet_68415 |
|
|
Rare sleep disorder
|
Orphanet_68354 |
|
|
Rare dystonic disorder
|
Orphanet_68363 |
|
|
Rare parkinsonian disorder
|
Orphanet_68402 |
|
|
Rare inborn errors of metabolism
|
Orphanet_68367 |
|
|
Tumor of hematopoietic and lymphoid tissues
|
Orphanet_68347 |
|
|
Adynamia episodica hereditaria
|
Orphanet_682 |
|
|
Rare hearing loss
|
Orphanet_68361 |
|
|
Congenital limb malformation
|
Orphanet_68378 |
|
|
Rare hypokinetic movement disorder
|
Orphanet_68402 |
|
|
Paramyotonia congenita of Von Eulenburg
|
Orphanet_684 |
|
|
Progressive supranuclear palsy
|
Orphanet_683 |
|
|
Hypokalemic periodic paralysis
|
Orphanet_681 |
|
|
Hyperkalemic periodic paralysis
|
Orphanet_682 |
|
|
Hereditary spastic paraparesis
|
Orphanet_685 |
|
