| 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.
|
Hereditary cancer of stomach
|
Orphanet_423776 |
|
|
Undifferentiated carcinoma of stomach
|
Orphanet_423786 |
|
|
Epithelial tumor of the appendix
|
Orphanet_423982 |
|
|
Mucinous cystadenocarcinoma of the pancreas
|
Orphanet_424053 |
|
|
Neuroendocrine neoplasm of the small intestine
|
Orphanet_423975 |
|
|
Neuroendocrine tumor of the small intestine
|
Orphanet_423975 |
|
|
OGCT of pancreas
|
Orphanet_424080 |
|
|
Pancreatic intraductal papillary mucinous carcinoma
|
Orphanet_424058 |
|
|
Combined oxidative phosphorylation defect type 20
|
Orphanet_420728 |
|
|
Combined oxidative phosphorylation defect type 21
|
Orphanet_420733 |
|
|
Pancreatic solid pseudopapillary carcinoma
|
Orphanet_424065 |
|
|
Ectodermal dysplasia-short stature syndrome
|
Orphanet_423454 |
|
|
DORV with subaortic or doubly committed VSD
|
Orphanet_423693 |
|
|
Malan overgrowth syndrome
|
Orphanet_420179 |
|
|
Visual snow syndrome
|
Orphanet_420556 |
|
