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| 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.
  
      
    
    
    
  
    
  | Sacrococcygeal teratoma | Orphanet_494421 |  | 
  | MIRAGE syndrome | Orphanet_494433 |  | 
  | Vulvar adenocarcinoma | Orphanet_494454 |  | 
  | Greither disease | Orphanet_495 |  | 
  | Deletion 9q33.3q34.11 | Orphanet_495818 |  | 
  | Monosomy 9q33.3q34.11 | Orphanet_495818 |  | 
  | Gershoni-Baruch syndrome | Orphanet_496693 |  | 
  | EVEN-plus syndrome | Orphanet_496751 |  | 
  | Harel-Yoon syndrome | Orphanet_496790 |  | 
  | Non-inflammatory vasculopathy | Orphanet_496924 |  | 
  | C12ORF65-related COXPD | Orphanet_497623 |  | 
  | Epidermolytic nevus | Orphanet_497737 |  | 
  | Lenk-Ploski syndrome | Orphanet_497906 |  | 
  | Amyloid lichen | Orphanet_49804 |  | 
  | Lichen amyloidosis | Orphanet_49804 |  |