| 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.
|
Berylliosis
|
Orphanet_133 |
|
|
PAVC
|
Orphanet_1330 |
|
|
Chronic berylliosis
|
Orphanet_133 |
|
|
Partial AVSD
|
Orphanet_1330 |
|
|
Cantrell deformity
|
Orphanet_1335 |
|
|
Cantrell syndrome
|
Orphanet_1335 |
|
|
Thoraco-abdominal syndrome
|
Orphanet_1335 |
|
|
Hyperkeratosis-hyperpigmentation syndrome
|
Orphanet_1336 |
|
|
Ostravik-Lindemann-Solberg syndrome
|
Orphanet_1338 |
|
|
Pentalogy of Cantrell
|
Orphanet_1335 |
|
|
Partial atrioventricular canal defect
|
Orphanet_1330 |
|
|
Familial prostate cancer
|
Orphanet_1331 |
|
|
Familial pancreatic cancer
|
Orphanet_1333 |
|
|
Chronic mucocutaneous candidiasis
|
Orphanet_1334 |
|
|
Medullary thyroid carcinoma
|
Orphanet_1332 |
|
