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.
ACS5
|
Orphanet_710 |
|
CMRD
|
Orphanet_71 |
|
DYT12
|
Orphanet_71517 |
|
FPD/AML
|
Orphanet_71290 |
|
FPDMM
|
Orphanet_71290 |
|
FPS/AML
|
Orphanet_71290 |
|
NMOSD
|
Orphanet_71211 |
|
Phenylketonuria
|
Orphanet_716 |
|
Anderson disease
|
Orphanet_71 |
|
Pfeiffer syndrome
|
Orphanet_710 |
|
Autoimmune thrombocytopenia
|
Orphanet_71203 |
|
Devic disease
|
Orphanet_71211 |
|
SCHAD deficiency
|
Orphanet_71212 |
|
Sandifer syndrome
|
Orphanet_71272 |
|
Rh-null syndrome
|
Orphanet_71275 |
|