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.
Penile adenocarcinoma
|
Orphanet_398053 |
|
Refractory CD
|
Orphanet_398063 |
|
Refractory sprue
|
Orphanet_398063 |
|
MAGEL2-related PWLS
|
Orphanet_398069 |
|
Schaaf-Yang syndrome
|
Orphanet_398069 |
|
Prader-Willi-like syndrome
|
Orphanet_398073 |
|
SIM1-related PWLS
|
Orphanet_398079 |
|
Neonatal AHA
|
Orphanet_398109 |
|
Neonatal AIHA
|
Orphanet_398109 |
|
Neonatal DM
|
Orphanet_398117 |
|
Neonatal dermatomyositis
|
Orphanet_398117 |
|
Neonatal scleroderma
|
Orphanet_398127 |
|
Oculoauriculofrontonasal syndrome
|
Orphanet_398156 |
|
Huntington chorea
|
Orphanet_399 |
|
Huntington disease
|
Orphanet_399 |
|