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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.
  
      
    
    
    
  
    
  | Azygos continuation of the inferior vena cava | Orphanet_99121 |  | 
  | Congenital stenosis of the inferior vena cava | Orphanet_99122 |  | 
  | Reticular dystrophy of the retinal pigment epithelium | Orphanet_99002 |  | 
  | Congenital anomaly of the tricuspid valve chordae | Orphanet_99055 |  | 
  | Congenital anomaly of tricuspid chordae tendineae | Orphanet_99055 |  | 
  | Congenital anomaly of tricuspid tendinous chords | Orphanet_99055 |  | 
  | Straddling and/or overriding mitral valve | Orphanet_99064 |  | 
  | Congenital stenosis or atresia of a coronary ostium | Orphanet_99087 |  | 
  | Dysgerminoma of ovary | Orphanet_99912 |  | 
  | Isolated sulfite oxidase deficiency | Orphanet_99731 |  | 
  | Complex regional pain syndrome type 1 | Orphanet_99995 |  | 
  | Complex regional pain syndrome type 2 | Orphanet_99994 |  | 
  | Cleft soft palate | Orphanet_99772 |  | 
  | Cleft velum palatinum | Orphanet_99772 |  | 
  | X-linked spastic paraplegia type 2 | Orphanet_99015 |  |