|   
  
    | Disease #00053
        
          | Official abbreviation | XPF |  
          | Name | Xeroderma pigmentosum, group F |  
          | OMIM ID | 278760 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | - |  
          | Individuals reported having this disease | 0 |  
          | Phenotype entries for this disease | 0 |  
          | Associated with 1 gene | ERCC4 |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  |  
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