Phenotypes for disease #03486 (DFNB89 (deafness, autosomal recessive, type 89 (DFNB89)), OMIM:613916)

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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     
0000319573 - Non-syndromic hearing impairment DFNB89 Familial, autosomal recessive - - - HP:0011474 - Yacouba Dia 00428668
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