Phenotypes for disease #03798 (DFNB18B (deafness, autosomal recessive, type 18b (DFNB-18B)), OMIM:614945)

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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     
0000319579 - Non-syndromic hearing impairment DFNB18B Familial, autosomal recessive - - - HP:0000399 - Yacouba Dia 00428674
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