| 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.
|
Kelly-Paterson syndrome
|
Orphanet_54028 |
|
|
Plummer-Vinson syndrome
|
Orphanet_54028 |
|
|
Sideropenic dysphagia
|
Orphanet_54028 |
|
|
Moschcowitz disease
|
Orphanet_54057 |
|
|
Labrune syndrome
|
Orphanet_542310 |
|
|
Benson syndrome
|
Orphanet_54247 |
|
|
Necrobiosis lipoidica
|
Orphanet_542592 |
|
|
Oppenheim-Urbach disease
|
Orphanet_542592 |
|
|
Spongy myocardium
|
Orphanet_54260 |
|
|
Livedoid vasculopathy
|
Orphanet_542643 |
|
|
Isolated hyperchlorhidrosis
|
Orphanet_542657 |
|
|
Hepatocellular adenoma
|
Orphanet_54272 |
|
|
Burkitt lymphoma
|
Orphanet_543 |
|
|
Mesangiocapillary glomerulonephritis
|
Orphanet_54370 |
|
|
Primary MPGN
|
Orphanet_54370 |
|
