| 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.
|
IMAM
|
Orphanet_247718 |
|
|
Lipoblastoma
|
Orphanet_247762 |
|
|
MEN2B
|
Orphanet_247709 |
|
|
Macroencephaly
|
Orphanet_2477 |
|
|
Megalencephaly
|
Orphanet_2477 |
|
|
Wagenmann-Froboese syndrome
|
Orphanet_247709 |
|
|
WNT4 deficiency
|
Orphanet_247768 |
|
|
Rokitansky sequence
|
Orphanet_247775 |
|
|
MUTYH-related AFAP
|
Orphanet_247798 |
|
|
MUTYH-related attenuated FAP
|
Orphanet_247798 |
|
|
Müllerian aplasia and hyperandrogenism
|
Orphanet_247768 |
|
|
X-linked cerebellar ataxia
|
Orphanet_247765 |
|
|
Müllerian duct failure and hyperandrogenism
|
Orphanet_247768 |
|
|
MUTYH-related attenuated familial adenomatous polyposis
|
Orphanet_247798 |
|
|
MUTYH-related attenuated familial polyposis coli
|
Orphanet_247798 |
|
