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.
Male infertility due to testicular dysgenesis or sperm disorder
|
Orphanet_399764 |
|
ALX3-related frontonasal dysplasia
|
Orphanet_391474 |
|
Persistent combined dystonia
|
Orphanet_391711 |
|
Rare genetic dystonia
|
Orphanet_391799 |
|
Rare genetic dystonic disorder
|
Orphanet_391799 |
|
Miyoshi muscular dystrophy type 3
|
Orphanet_399096 |
|
Femoral head epiphysiolysis
|
Orphanet_399329 |
|
Ovarian malignant epithelial tumor
|
Orphanet_398934 |
|
Neonatal lupus erythematosus
|
Orphanet_398124 |
|
Persistent idiopathic facial pain
|
Orphanet_398147 |
|
Slipped capital femoral epiphysis
|
Orphanet_399329 |
|
Slipped upper femoral epiphysis
|
Orphanet_399329 |
|
Osteonecrosis of genetic origin
|
Orphanet_399380 |
|
Osteochondrosis of genetic origin
|
Orphanet_399391 |
|
Adult-onset myasthenia gravis
|
Orphanet_391490 |
|