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.
Lichen amyloidosus
|
Orphanet_49804 |
|
Rogers syndrome
|
Orphanet_49827 |
|
Aquagenic keratoderma
|
Orphanet_498359 |
|
Mirror-image polydactyly
|
Orphanet_498494 |
|
Sugarman brachydactyly
|
Orphanet_498602 |
|
Sugarman-Hager-Kulik syndrome
|
Orphanet_498602 |
|
Kerion celsi
|
Orphanet_499 |
|
Congenital syphilis
|
Orphanet_499009 |
|
Idiopathic OPN
|
Orphanet_499107 |
|
Calcifying epitheliocarcinoma
|
Orphanet_499182 |
|
Malignant pilomatricoma
|
Orphanet_499182 |
|
Pilomatrix carcinoma
|
Orphanet_499182 |
|
Trichomatrical carcinoma
|
Orphanet_499182 |
|
Familial monosomy 7 syndrome
|
Orphanet_495930 |
|
DGI without OI
|
Orphanet_49042 |
|