Search Ontology: 
        
        Human Disease
            autosomal dominant nonsyndromic deafness 77
- Term ID
 - DOID:0112168
 - Synonyms
 - 
    
        
        
- DFNA77
 
 - Definition
 - An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ABCC1 gene on chromosome 16p13.11. https://pubmed.ncbi.nlm.nih.gov/31273342/
 - References
 - Ontology
 - Human Disease ( DOID:0112168 )
 
                
                    
                        Other Pages
                    
                    
                
                
            
        
        
    
        
            
            
 
    
        
    
    
        
        
    
    
    
                
                    
                        Genes Involved
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Zebrafish Models