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    | Disease #05725 (RP80 (retinitis pigmentosa, type 80 (RP80)), OMIM:617781)
        
          | Official abbreviation | RP80 |  
          | Name | retinitis pigmentosa, type 80 (RP80) |  
          | OMIM ID | 617781 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | Autosomal recessive |  
          | Individuals reported having this disease | - |  
          | Phenotype entries for this disease | - |  
          | Associated with 1 gene | IFT140 |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  
          | Date created | 2020-04-10 19:43:17 +02:00 (CEST) |  
          | Date last edited | N/A |  |  
 
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