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.
Nievergelt syndrome
|
Orphanet_2633 |
|
MRCS syndrome
|
Orphanet_263347 |
|
Thymoma type A
|
Orphanet_263310 |
|
Thymoma type AB
|
Orphanet_263324 |
|
Thymoma type B
|
Orphanet_263317 |
|
Mesomelic dwarfism, Nievergelt type
|
Orphanet_2633 |
|
Mesomelic dysplasia, Nievergelt type
|
Orphanet_2633 |
|
Primary thymic epithelial neoplasm type A
|
Orphanet_263310 |
|
Primary thymic epithelial neoplasm type AB
|
Orphanet_263324 |
|
Primary thymic epithelial neoplasm type B
|
Orphanet_263317 |
|
Primary thymic epithelial tumor type A
|
Orphanet_263310 |
|
Primary thymic epithelial tumor type AB
|
Orphanet_263324 |
|
Primary thymic epithelial tumor type B
|
Orphanet_263317 |
|
Well-differentiated thymic neuroendocrine carcinoma
|
Orphanet_263331 |
|
Moderately-differentiated thymic neuroendocrine carcinoma
|
Orphanet_263335 |
|