Phenotypes for disease #02908 (DFNB49 (deafness, autosomal recessive, type 49 (DFNB-49)), OMIM:610153)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000319224 Post-lingual Non-syndromic hearing impairment, with variable age of onset with two family members with onset at 12 years of age and a third family member with onset at 8 years of age. Post lingual Non-syndromic hearing impairment Post lingual Non-syndromic hearing impairment Familial, autosomal recessive 8y, 12y - - HP:0008596 - Yacouba Dia 00428320
0000319233 see paper; ..., bilateral hearing loss (moderate to profound) non-syndromic hearing impairment DFNB49 Familial, autosomal recessive - - - HP:0011474 - Yacouba Dia 00428324
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