Disease #00089
      
        
          | Official abbreviation | 
          DFNB97 |  
        
          | Name | 
          Deafness, autosomal recessive 97 |  
        
          | OMIM ID | 
          616705 |  
        
          | Human Phenotype Ontology Project (HPO) | 
          HPO |  
        
          | Inheritance | 
          - |  
        
          | Individuals reported having this disease | 
          0 |  
        
          | Phenotype entries for this disease | 
          0 |  
        
          | Associated with 1 gene | 
          MET |  
        
          | Associated tissues | 
          - |  
        
          | Disease features | 
          - |  
        
          | Remarks | 
          - |   
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