Phenotypes for disease #06877 (DFNA (deafness, nonsyndromic (DFNA, autosomal dominant)))

8 entries on 1 page. Showing entries 1 - 8.
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AscendingPhenotype ID     

Diagnosis/Initial     

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Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

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Individual ID     
0000290113 bilateral progressive hearing loss bilateral progressive hearing loss - Familial, autosomal dominant - - - - David Baux 00396953
0000319215 non-syndromic autosomal dominant hearing impairment DFNA27 3y-hearing impairment, progressive Familial, autosomal dominant 12y 03y - HP:0011474 Yacouba Dia 00428310
0000319216 non-syndromic hearing impairment DFNA80 profound bilateral, symmetrical sensorineural hearing impairment (HP:0000365); no enal tubular dysfunction (-HP:0000124) Familial, autosomal dominant - - - - Yacouba Dia 00428311
0000319570 sensorineural hearing loss DFNA27 see paper; ..., progressive, non-syndromic, sensorineural hearing loss Familial, autosomal dominant - - - - Johan den Dunnen 00428665
0000325276 Autosomal dominant non-syndromic hearing impairment - - Familial, autosomal dominant - - - - Barbara Vona 00435034
0000330554 autosomal dominant non-syndromic hearing loss DFNA73 see paper; ... Familial, autosomal dominant - - - - Johan den Dunnen 00132291
0000330902 autosomal dominant non-syndromic hearing loss DFNA73 see paper; ... Familial, autosomal dominant - - - - Johan den Dunnen 00441462
0000337687 Severe hearing loss - - Unknown - - - - Hina Khan 00448506
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