| 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.
|
UAPA
|
Orphanet_980 |
|
|
UPD(15)mat
|
Orphanet_98754 |
|
|
UPD(15)pat
|
Orphanet_98795 |
|
|
Uveitis
|
Orphanet_98715 |
|
|
Vitreoretinopathy
|
Orphanet_98668 |
|
|
dHMN6
|
Orphanet_98920 |
|
|
dSMA1
|
Orphanet_98920 |
|
|
sACL
|
Orphanet_98841 |
|
|
CDA type 2
|
Orphanet_98873 |
|
|
Huntington disease-like 2
|
Orphanet_98934 |
|
|
CDA type 3
|
Orphanet_98870 |
|
|
Huntington disease-like 4
|
Orphanet_98759 |
|
|
Syndrome with 46,XY DSD
|
Orphanet_98087 |
|
|
Syndrome with 46,XY difference of sex development
|
Orphanet_98087 |
|
|
Syndrome with 46,XY disorder of sex development
|
Orphanet_98087 |
|
