| 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.
|
CMT6
|
Orphanet_90120 |
|
|
CMTDI
|
Orphanet_90114 |
|
|
HMSNP
|
Orphanet_90117 |
|
|
MADA
|
Orphanet_90153 |
|
|
Eosinophilic cellulitis
|
Orphanet_901 |
|
|
Wells syndrome
|
Orphanet_901 |
|
|
HMSN 6
|
Orphanet_90120 |
|
|
HMSN VI
|
Orphanet_90120 |
|
|
Centrifugal lipodystrophy
|
Orphanet_90156 |
|
|
Lipoatrophia semicircularis
|
Orphanet_90160 |
|
|
Semicircular lipoatrophy
|
Orphanet_90160 |
|
|
Meige disease
|
Orphanet_90186 |
|
|
Meige lymphedema
|
Orphanet_90186 |
|
|
Autosomal recessive Charcot-Marie-Tooth disease, Ouvrier type
|
Orphanet_90118 |
|
|
Lipodystrophia centrifugalis abdominalis infantilis
|
Orphanet_90156 |
|
