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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.
  
      
    
    
    
  
    
  | 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 |  |