| 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.
|
ASAN
|
Orphanet_231466 |
|
|
ATMDS
|
Orphanet_231401 |
|
|
Buckley syndrome
|
Orphanet_2314 |
|
|
Job syndrome
|
Orphanet_2314 |
|
|
Alpha-thalassemia-myelodysplastic syndrome
|
Orphanet_231401 |
|
|
Pharyngeal-cervical-brachial weakness
|
Orphanet_231426 |
|
|
Acute pandysautonomia
|
Orphanet_231457 |
|
|
Variant of GBS
|
Orphanet_231413 |
|
|
Acute panautonomic GBS
|
Orphanet_231457 |
|
|
Variant of Guillain-Barré syndrome
|
Orphanet_231413 |
|
|
Acute panautonomic Guillain-Barré syndrome
|
Orphanet_231457 |
|
|
Acquired hemoglobin H disease
|
Orphanet_231401 |
|
|
Autosomal dominant HIES due to STAT3 deficiency
|
Orphanet_2314 |
|
|
Acute sensory ataxic GBS
|
Orphanet_231466 |
|
|
Acute sensory ataxic Guillain-Barré syndrome
|
Orphanet_231466 |
|
