Phenotypes for disease #02355 (DFNA9 (deafness, autosomal dominant, type 9 (DFNA-9)), OMIM:601369)

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     
0000045619 Late onset (18-30y), progressive high-tone hearing loss - - Familial, autosomal dominant - - - - - Zippi Brownstein 00059030
0000078608 - - - Unknown - - - - - Margit Schraders 00100385
0000319322 - Non-syndromic tearing impairment Non-syndromic tearing impairment Familial, autosomal recessive - - - HP:0000399 - Yacouba Dia 00428417
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