| 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.
|
Benign vascular tumor
|
Orphanet_673470 |
|
|
Borderline vascular tumor
|
Orphanet_673473 |
|
|
Rare genetic tumor
|
Orphanet_68336 |
|
|
Rare bone tumor
|
Orphanet_68411 |
|
|
Malignant rhabdoid tumor
|
Orphanet_69077 |
|
|
Rare epithelial tumor of stomach
|
Orphanet_63443 |
|
|
Locally aggressive tumors
|
Orphanet_673473 |
|
|
Bartter syndrome type 1
|
Orphanet_620217 |
|
|
Mosaic neurofibromatosis type 1
|
Orphanet_634461 |
|
|
Nonmosaic neurofibromatosis type 1
|
Orphanet_636 |
|
|
Perrault syndrome type 1
|
Orphanet_642945 |
|
|
Charcot-Marie-Tooth disease type 1
|
Orphanet_65753 |
|
|
Charcot-Marie-Tooth neuropathy type 1
|
Orphanet_65753 |
|
|
3-methylglutaconic aciduria type 1
|
Orphanet_67046 |
|
|
Seemanova syndrome type 2
|
Orphanet_647 |
|
