| manager | 
	
		
		
	 | 
 
	| language | 
	- | 
 
| license | 
- | 
 
| created at | 
2021-12-22 03:08:20 UTC | 
 
| updated at | 
2021-12-22 07:06:09 UTC | 
 
 
 
 | 
 
MONDO_bioport_pref_name
 
 | 
  183,974 entries
      
 | 
There is 0 pattern entry.
  
      
    
    
    
  
    
  | 
    ACRDYS1
   | 
  
    7044   | 
  
    
   | 
  | 
    ADOHR
   | 
  
    7044   | 
  
    
   | 
  | 
    acrodysostosis 1
   | 
  
    7044   | 
  
    
   | 
  | 
    infantile, type 1 polycystic kidney disease
   | 
  
    D017044   | 
  
    
   | 
  | 
    polycystic kidney and hepatic disease 1 (autosomal recessive)
   | 
  
    D017044   | 
  
    
   | 
  | 
    kidney, polycystic, autosomal recessive
   | 
  
    D017044   | 
  
    
   | 
  | 
    polycystic kidney, autosomal recessive
   | 
  
    D017044   | 
  
    
   | 
  | 
    polycystic kidney disease, infantile, type i
   | 
  
    D017044   | 
  
    
   | 
  | 
    infantile, type i polycystic kidney disease
   | 
  
    D017044   | 
  
    
   | 
  | 
    oculocutaneous albinism, minimal pigment type
   | 
  
    C537044   | 
  
    
   | 
  | 
    adult familial nephronophthisis-spastic quadriparesia syndrome
   | 
  
    17044   | 
  
    
   | 
  | 
    albinism, minimal pigment type
   | 
  
    C537044   | 
  
    
   | 
  | 
    polycystic, autosomal recessive kidney
   | 
  
    D017044   | 
  
    
   | 
  | 
    minimal pigment type albinism
   | 
  
    C537044   | 
  
    
   | 
  | 
    minimal pigment type oculocutaneous albinism
   | 
  
    C537044   | 
  
    
   |