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.
MCOPS7
|
Orphanet_2556 |
|
MILS
|
Orphanet_255210 |
|
Microsporidiosis
|
Orphanet_2552 |
|
PDHBD
|
Orphanet_255138 |
|
Dopa-responsive dystonia
|
Orphanet_255 |
|
Diaphorase deficiency
|
Orphanet_255182 |
|
Navajo neurohepatopathy
|
Orphanet_255229 |
|
Navajo neuropathy
|
Orphanet_255229 |
|
Meier-Gorlin syndrome
|
Orphanet_2554 |
|
MIDAS syndrome
|
Orphanet_2556 |
|
MLS syndrome
|
Orphanet_2556 |
|
Mietens syndrome
|
Orphanet_2557 |
|
Mikati-Najjar-Sahli syndrome
|
Orphanet_2558 |
|
Pyruvate dehydrogenase E1-beta deficiency
|
Orphanet_255138 |
|
Pyruvate dehydrogenase E3-binding protein deficiency
|
Orphanet_255182 |
|