Disease #03182 (LCA13;RP53 (Leber congenital amaurosis, type 13 (LCA13, retinitis pigmentosa, type 53 (RP53))), OMIM:612712)
      
        
          | Official abbreviation | 
          LCA13;RP53 |  
        
          | Name | 
          Leber congenital amaurosis, type 13 (LCA13, retinitis pigmentosa, type 53 (RP53)) |  
        
          | OMIM ID | 
          612712 |  
        
          | Human Phenotype Ontology Project (HPO) | 
          HPO |  
        
          | Inheritance | 
          Autosomal dominant, Autosomal recessive |  
        
          | Individuals reported having this disease | 
          2 |  
        
          | Phenotype entries for this disease | 
          2 |  
        
          | Associated with 1 gene | 
          RDH12 |  
        
          | Associated tissues | 
          - |  
        
          | Disease features | 
          - |  
        
          | Remarks | 
          - |  
        
          | Date created | 
          2014-09-25 23:29:40 +02:00 (CEST) |  
        
          | Date last edited | 
          2021-12-10 21:51:32 +01:00 (CET) |   
  
      Individuals
      
      
       
      
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