| 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.
|
Beta-mannosidosis
|
Orphanet_118 |
|
|
IOSCA
|
Orphanet_1186 |
|
|
SPAX7
|
Orphanet_1182 |
|
|
Beta-mannosidase deficiency
|
Orphanet_118 |
|
|
Boucher-Neuhäuser syndrome
|
Orphanet_1180 |
|
|
Ataxo-opso-myoclonus syndrome
|
Orphanet_1183 |
|
|
Kinsbourne syndrome
|
Orphanet_1183 |
|
|
OMA syndrome
|
Orphanet_1183 |
|
|
Opsoclonus-myoclonus syndrome
|
Orphanet_1183 |
|
|
Opsoclonus-myoclonus-ataxia syndrome
|
Orphanet_1183 |
|
|
POMA syndrome
|
Orphanet_1183 |
|
|
Paraneoplastic opsoclonus-myoclonus
|
Orphanet_1183 |
|
|
Fenton-Wilkinson-Toselano syndrome
|
Orphanet_1184 |
|
|
Ohaha syndrome
|
Orphanet_1186 |
|
|
Ophthalmoplegia-hypotonia-ataxia-hypoacusis-athetosis syndrome
|
Orphanet_1186 |
|
