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.
Heimler syndrome
|
Orphanet_3220 |
|
PRPS1 superactivity
|
Orphanet_3222 |
|
Pfeiffer-Kapferer syndrome
|
Orphanet_3224 |
|
Tungland-Bellman syndrome
|
Orphanet_3225 |
|
Deafness-oligodontia syndrome
|
Orphanet_3230 |
|
Deafness-onychodystrophy syndrome
|
Orphanet_3231 |
|
Sellars-Beighton syndrome
|
Orphanet_3232 |
|
Stapedo-vestibular ankylosis
|
Orphanet_3235 |
|
Thies-Reis syndrome
|
Orphanet_3235 |
|
Jackson-Barr syndrome
|
Orphanet_3236 |
|
Symphalangism-brachydactyly syndrome
|
Orphanet_3237 |
|
WL syndrome
|
Orphanet_3237 |
|
Cardiospondylocarpofacial syndrome
|
Orphanet_3238 |
|
Forney syndrome
|
Orphanet_3238 |
|
Forney-Robinson-Pascoe syndrome
|
Orphanet_3238 |
|