| 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.
|
Hereditary cystic renal disease
|
Orphanet_93587 |
|
|
Short limb skeletal dysplasia with SCID
|
Orphanet_935 |
|
|
Acquired thrombotic thrombocytopenic purpura
|
Orphanet_93585 |
|
|
Autoimmune thrombotic thrombocytopenic purpura
|
Orphanet_93585 |
|
|
Immune-mediated thrombotic thrombocytopenic purpura
|
Orphanet_93585 |
|
|
Nephropathy secondary to a storage or other metabolic disease
|
Orphanet_93593 |
|
|
Mixed cryoglobulinemia type II
|
Orphanet_93554 |
|
|
Mixed cryoglobulinemia type III
|
Orphanet_93555 |
|
|
Atypical hemolytic uremic syndrome with anti-factor H antibodies
|
Orphanet_93581 |
|
|
Renal or urinary tract malformation
|
Orphanet_93545 |
|
|
Atypical HUS with anti-factor H antibodies
|
Orphanet_93581 |
|
