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.
Thymoma
|
Orphanet_99867 |
|
Albinism-deafness syndrome
|
Orphanet_998 |
|
Unilateral megalencephaly
|
Orphanet_99802 |
|
Haddad syndrome
|
Orphanet_99803 |
|
Ondine-Hirschsprung disease
|
Orphanet_99803 |
|
Ondine-Hirschsprung syndrome
|
Orphanet_99803 |
|
Oculootodental syndrome
|
Orphanet_99806 |
|
PEHO-like syndrome
|
Orphanet_99807 |
|
Familial porencephaly
|
Orphanet_99810 |
|
LIG4 syndrome
|
Orphanet_99812 |
|
Lassa fever
|
Orphanet_99824 |
|
Nipah encephalitis
|
Orphanet_99825 |
|
Nipah fever
|
Orphanet_99825 |
|
Congo fever
|
Orphanet_99827 |
|
Dengue fever
|
Orphanet_99828 |
|