| 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.
|
Mitochondrial membrane transport disorder
|
Orphanet_254827 |
|
|
Lichen planus tropicus
|
Orphanet_254395 |
|
|
Epithelioid trophoblastic tumor
|
Orphanet_254698 |
|
|
Spinocerebellar ataxia with epilepsy
|
Orphanet_254881 |
|
|
Exercise intolerance with lactic acidosis
|
Orphanet_254843 |
|
|
OXPHOS disease with no known mechanism
|
Orphanet_254822 |
|
|
Oculoauriculovertebral spectrum with radial defects
|
Orphanet_2549 |
|
|
Mitochondrial myopathy with reversible COX deficiency
|
Orphanet_254864 |
|
|
Mitochondrial myopathy with reversible complex IV deficiency
|
Orphanet_254864 |
|
|
Genetic hyperferritinemia without iron overload
|
Orphanet_254704 |
|
