| 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.
|
ABPA
|
Orphanet_1164 |
|
|
AOA1
|
Orphanet_1168 |
|
|
Aspergillosis
|
Orphanet_1163 |
|
|
Beckwith-Wiedemann syndrome
|
Orphanet_116 |
|
|
Exomphalos-macroglossia-gigantism syndrome
|
Orphanet_116 |
|
|
Wiedemann-Beckwith syndrome
|
Orphanet_116 |
|
|
Chylous ascites
|
Orphanet_1160 |
|
|
Allergic aspergillosis
|
Orphanet_1164 |
|
|
Hinson-Pepys disease
|
Orphanet_1164 |
|
|
Allergic bronchopulmonary aspergillosis
|
Orphanet_1164 |
|
|
Isolated asymmetric crying facies
|
Orphanet_1166 |
|
|
Congenital unilateral hypoplasia of depressor anguli oris
|
Orphanet_1166 |
|
|
Ataxia-oculomotor apraxia type 1
|
Orphanet_1168 |
|
