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.
APS3
|
Orphanet_227982 |
|
APS4
|
Orphanet_227990 |
|
Diphallia
|
Orphanet_227 |
|
MSA-c
|
Orphanet_227510 |
|
IFAP syndrome
|
Orphanet_2273 |
|
Dykes-Marks-Harper syndrome
|
Orphanet_2274 |
|
Fundus albipunctatus
|
Orphanet_227796 |
|
Passwell-Goodman-Siprkowski syndrome
|
Orphanet_2278 |
|
APS type 3
|
Orphanet_227982 |
|
APS type 4
|
Orphanet_227990 |
|
Sporadic olivopontocerebellar atrophy type 1
|
Orphanet_227510 |
|
Multiple system atrophy, cerebellar type
|
Orphanet_227510 |
|
Familial breast cancer
|
Orphanet_227535 |
|
Hereditary breast cancer
|
Orphanet_227535 |
|
Familial breast carcinoma
|
Orphanet_227535 |
|