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.
Wormian bones-micrognathia-abnormal dentition-progeroid syndrome
|
Orphanet_659873 |
|
Bilateral acute depigmentation of the iris
|
Orphanet_69736 |
|
Dermatomyositis sine dermatitis
|
Orphanet_645626 |
|
Cutaneous reactive dermatoses
|
Orphanet_673574 |
|
Microcephaly-short stature-intellectual disability syndrome
|
Orphanet_658595 |
|
Aplastic anemia-intellectual disability-dwarfism syndrome
|
Orphanet_611216 |
|
Von Recklinghausen disease
|
Orphanet_636 |
|
Glaucomatocyclitic crisis disease
|
Orphanet_636950 |
|
IgG4-related thyroid disease
|
Orphanet_64744 |
|
X-linked Charcot-Marie-Tooth disease
|
Orphanet_64747 |
|
Brittle bone disease
|
Orphanet_666 |
|
Glass bone disease
|
Orphanet_666 |
|
Rare vascular disease
|
Orphanet_68362 |
|
Rare metabolic disease
|
Orphanet_68367 |
|
Rare infectious disease
|
Orphanet_68416 |
|