| 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.
|
Syndromic retinal dystrophy
|
Orphanet_519325 |
|
|
Isolated congenital entropion
|
Orphanet_519386 |
|
|
Congenital cystic eye
|
Orphanet_519384 |
|
|
Structural developmental eye defect
|
Orphanet_519272 |
|
|
Secondary early-onset glaucoma
|
Orphanet_519331 |
|
|
Isolated foveal hypoplasia
|
Orphanet_519398 |
|
|
Isolated progressive inherited retinal disorder
|
Orphanet_519306 |
|
|
Isolated stationary inherited retinal disorder
|
Orphanet_519319 |
|
|
Rare disorder involving multiple structures of the eye
|
Orphanet_519329 |
|
|
Inflammatory/autoimmune disorder involving the lacrimal system
|
Orphanet_519264 |
|
|
Syndromic ectopia lentis
|
Orphanet_519292 |
|
|
Acute myelogenous leukemia
|
Orphanet_519 |
|
|
Acute myeloid leukemia
|
Orphanet_519 |
|
|
Rare ocular motility/alignment disorder
|
Orphanet_519355 |
|
|
Rare optic nerve disorder
|
Orphanet_519351 |
|
