Phenotypes for disease #02370 (DFNA12 (deafness, autosomal dominant, type 12 (DFNA-12)), OMIM:601543)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000045616 Childhood onset, 2-4y, moderate-severe hearing loss - - Familial, autosomal dominant - - - - - Zippi Brownstein 00059027
0000046745 Congenital, progressive, moderate-profound NSHL - - Familial, autosomal dominant - - - - - Zippi Brownstein 00060256
0000046746 Congenital, progressive, severe-profound NSHL - - Familial, autosomal dominant - - - - - Zippi Brownstein 00060257
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