| 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.
|
Mucormycosis
|
Orphanet_73263 |
|
|
Paracoccidioidomycosis
|
Orphanet_73260 |
|
|
Polymyositis
|
Orphanet_732 |
|
|
Zygomycosis
|
Orphanet_73263 |
|
|
Müllerian aplasia
|
Orphanet_73217 |
|
|
HANAC syndrome
|
Orphanet_73229 |
|
|
Central neurocytoma
|
Orphanet_73256 |
|
|
Hypernychthemeral syndrome
|
Orphanet_73267 |
|
|
IGF-1 deficiency
|
Orphanet_73272 |
|
|
Resistance to IGF-1
|
Orphanet_73273 |
|
|
Kidney tubulopathy-dilated cardiomyopathy syndrome
|
Orphanet_73224 |
|
|
Global developmental delay-osteopenia-ectodermal defect syndrome
|
Orphanet_73223 |
|
|
Ossification anomalies-psychomotor developmental delay syndrome
|
Orphanet_73230 |
|
|
Growth delay-deafness-intellectual disability syndrome
|
Orphanet_73272 |
|
|
Bleeding diathesis due to a collagen receptor defect
|
Orphanet_73271 |
|
