Phenotypes for disease #02580 (DFNA22 (deafness, autosomal dominant, type 22 (DFNA-22)), OMIM:606346)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000045617 Teen onset (12-17y), moderate-profound hearing loss - - Familial, autosomal dominant - - - - - Zippi Brownstein 00059028
0000280134 Hearing impairment, Sensorineural hearing impairment, Hyperactivity, sister also affected (untested) - - Familial, autosomal dominant 06y - - - - Andreas Laner 00386331
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