| 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.
|
Hereditary combined deficiency of factors II, VII, IX and X
|
Orphanet_98434 |
|
|
Partial autosomal deletion
|
Orphanet_98142 |
|
|
ATR syndrome, deletion type
|
Orphanet_98791 |
|
|
Ataxia with dementia
|
Orphanet_98538 |
|
|
Rare cerebrovascular dementia
|
Orphanet_98549 |
|
|
Acute idiopathic demyelinating polyneuropathy
|
Orphanet_98916 |
|
|
Acute inflammatory demyelinating polyradiculoneuropathy
|
Orphanet_98916 |
|
|
Histiocytic and dendritic cell tumor
|
Orphanet_98287 |
|
|
Rare immune disease
|
Orphanet_98004 |
|
|
Rare neurologic disease
|
Orphanet_98006 |
|
|
Rare odontologic disease
|
Orphanet_98026 |
|
|
Rare otorhinolaryngologic disease
|
Orphanet_98036 |
|
|
Immunodeficiency-associated lymphoproliferative disease
|
Orphanet_98290 |
|
|
Hereditary stomatocytic disease
|
Orphanet_98365 |
|
|
Alpha granule disease
|
Orphanet_98455 |
|
