| 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.
|
Mirizzi syndrome
|
Orphanet_521219 |
|
|
Xq25 microtriplication
|
Orphanet_521258 |
|
|
SINO syndrome
|
Orphanet_521390 |
|
|
Dystonia-parkinsonism-hypermanganesemia syndrome
|
Orphanet_521406 |
|
|
ATP1A1-related CMT2
|
Orphanet_521414 |
|
|
Baker-Gordon syndrome
|
Orphanet_522077 |
|
|
Hereditary leiomyomatosis
|
Orphanet_523 |
|
|
Reed syndrome
|
Orphanet_523 |
|
|
Pediatric-onset glaucoma
|
Orphanet_523000 |
|
|
DDON syndrome
|
Orphanet_52368 |
|
|
Mohr-Tranebjaerg syndrome
|
Orphanet_52368 |
|
|
Li-Fraumeni syndrome
|
Orphanet_524 |
|
|
MALT lymphoma
|
Orphanet_52417 |
|
|
Branchiootic syndrome
|
Orphanet_52429 |
|
|
Lichen follicularis
|
Orphanet_525 |
|
