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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.
  
      
    
    
    
  
    
  | Secondary non-traumatic AVN | Orphanet_399180 |  | 
  | Secondary non-traumatic avascular necrosis | Orphanet_399180 |  | 
  | Late-onset distal crystallinopathy | Orphanet_399058 |  | 
  | Rare hereditary disease with avascular necrosis | Orphanet_399185 |  | 
  | KLHL9-related early-onset distal myopathy | Orphanet_399081 |  | 
  | Nebulin-related early-onset distal myopathy | Orphanet_399103 |  | 
  | Male infertility due to asthenozoospermia | Orphanet_399813 |  | 
  | Male infertility due to gonadal dysgenesis or sperm disorder | Orphanet_399764 |  | 
  | Rare disorder due to impaired sperm transport | Orphanet_399824 |  | 
  | Male infertility due to sperm disorder | Orphanet_399771 |  | 
  | Male infertility due to sperm motility disorder | Orphanet_399813 |  | 
  | Male infertility due to testicular dysgenesis or sperm disorder | Orphanet_399764 |  | 
  | Miyoshi muscular dystrophy type 3 | Orphanet_399096 |  | 
  | Femoral head epiphysiolysis | Orphanet_399329 |  | 
  | Slipped capital femoral epiphysis | Orphanet_399329 |  |