Search Ontology: 
        
        Human Disease
            autosomal recessive nonsyndromic deafness 67
- Term ID
 - DOID:0110518
 - Synonyms
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- autosomal recessive deafness 67
 - DFNB67
 
 - Definition
 - An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the LHFPL5 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/16459341
 - References
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- ICD10CM:H90.3
 - MIM:610265
 
 - Ontology
 - Human Disease ( DOID:0110518 )
 
                
                    
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                        Zebrafish Models