| 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.
|
Non-syndromic congenital functional defect of phagocytes
|
Orphanet_674896 |
|
|
Non-syndromic constitutional functional phagocyte defect
|
Orphanet_674896 |
|
|
Acquired elastotic haemangioma
|
Orphanet_675597 |
|
|
Eccrine angiomatous hamartoma
|
Orphanet_673568 |
|
|
Vegetant intravascular hemangioendothelioma
|
Orphanet_673525 |
|
|
Papillary capillary hemangioma
|
Orphanet_673543 |
|
|
Targetoid hemosiderotic hemangioma
|
Orphanet_675362 |
|
|
Large segmental hemangioma
|
Orphanet_675380 |
|
|
Littoral cell hemangioma of the spleen
|
Orphanet_673538 |
|
|
Pleural mesothelioma in situ
|
Orphanet_675841 |
|
|
Peritoneal mesothelioma in situ
|
Orphanet_676036 |
|
|
Isolated segmental infantile hemangioma
|
Orphanet_675380 |
|
|
Masson's vegetant intravascular hemangiendothelioma
|
Orphanet_673525 |
|
|
Autosomal dominant late-onset retinal degeneration
|
Orphanet_67042 |
|
|
Chronic lymphocytic leukemia
|
Orphanet_67038 |
|
