| 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.
|
SPG5A
|
Orphanet_100986 |
|
|
SPG6
|
Orphanet_100988 |
|
|
SPG8
|
Orphanet_100989 |
|
|
mu-HCD
|
Orphanet_100024 |
|
|
Louis-Bar syndrome
|
Orphanet_100 |
|
|
Reticular perineurioma
|
Orphanet_100000 |
|
|
Sclerosing perineurioma
|
Orphanet_100001 |
|
|
Extraneural perineurioma
|
Orphanet_100002 |
|
|
Intraneural perineurioma
|
Orphanet_100003 |
|
|
ABetaE22Q amyloidosis
|
Orphanet_100006 |
|
|
ACys amyloidosis
|
Orphanet_100008 |
|
|
CST3-related amyloidosis
|
Orphanet_100008 |
|
|
Cystatin amyloidosis
|
Orphanet_100008 |
|
|
Mediterranean lymphoma
|
Orphanet_100025 |
|
|
Franklin disease
|
Orphanet_100026 |
|
