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.
POADS
|
Orphanet_246 |
|
VDEGS
|
Orphanet_2460 |
|
Miller syndrome
|
Orphanet_246 |
|
Postaxial acrodysostosis
|
Orphanet_246 |
|
Marden-Walker-like syndrome
|
Orphanet_2460 |
|
Marden-Walker syndrome
|
Orphanet_2461 |
|
Shprintzen-Goldberg syndrome
|
Orphanet_2462 |
|
Fragoso-CantĂș syndrome
|
Orphanet_2463 |
|
MASA syndrome
|
Orphanet_2466 |
|
Systemic mastocytosis
|
Orphanet_2467 |
|
Marfanoid syndrome, De Silva type
|
Orphanet_2464 |
|
Van den Ende-Gupta syndrome
|
Orphanet_2460 |
|
Acrofacial dysostosis, Genee-Wiedemann type
|
Orphanet_246 |
|
Postaxial acrofacial dysostosis
|
Orphanet_246 |
|
Marfanoid craniosynostosis syndrome
|
Orphanet_2462 |
|