Phenotypes for disease #02851 (DFNB48 (deafness, autosomal recessive, type 48 (DFNB48)), OMIM:609439)

8 entries on 1 page. Showing entries 1 - 8.
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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     
0000025759 - - - Unknown - - - - - Celia Zazo-Seco 00029679
0000025761 non syndromic hearing impairment - - Familial, autosomal recessive - - - - - Johan den Dunnen 00029794
0000025762 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00029795
0000025763 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00029798
0000025764 - - - Unknown - - - - - Celia Zazo-Seco 00029681
0000025765 - - - Unknown - - - - - Celia Zazo-Seco 00029683
0000025766 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00029799
0000025767 - - - Familial, autosomal recessive - - - - - Johan den Dunnen 00029800
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