| 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.
|
SYNGAP1-related DEE
|
Orphanet_544254 |
|
|
Infection-related HUS
|
Orphanet_544482 |
|
|
Bachmann-Bupp syndrome
|
Orphanet_544488 |
|
|
Follicular lymphoma
|
Orphanet_545 |
|
|
Non-Hodgkin lymphoma
|
Orphanet_547 |
|
|
Legionnaires disease
|
Orphanet_549 |
|
|
Diffuse large B-cell lymphoma
|
Orphanet_544 |
|
|
Primary cutaneous CD30+ T-cell lymphoproliferative disease
|
Orphanet_541 |
|
|
RNF13-related severe EOEE
|
Orphanet_544503 |
|
|
S. pneumoniae-associated HUS
|
Orphanet_544493 |
|
|
Primary cutaneous Ki-1+ T-cell lymphoproliferative disease
|
Orphanet_541 |
|
|
Ocular albinism, Nettleship-Falls type
|
Orphanet_54 |
|
|
Carbonic anhydrase XII deficiency
|
Orphanet_542657 |
|
|
Corticosteroid-sensitive aseptic abscess syndrome
|
Orphanet_54251 |
|
|
Aseptic systemic abscesses
|
Orphanet_54251 |
|
