Phenotypes for disease #02748 (DFNB39 (deafness, autosomal recessive, type 39 (DFNB-39)), OMIM:608265)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000337683 - Severe Hearing loss, Asymmetric - Unknown - - - - - Hina Khan 00448500
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