Phenotypes for disease #03303 (DFNB79 (deafness, autosomal recessive, type 79 (DFNB-79)), OMIM:613307)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000034284 see paper; … - - Familial, autosomal recessive - - - - - Jacopo Celli 00046602
0000034285 see paper; … - - Familial, autosomal recessive - - - - - Jacopo Celli 00046603
0000034286 see paper; … - - Familial, autosomal recessive - - - - - Jacopo Celli 00046604
0000034287 see paper; … - - Familial, autosomal recessive - - - - - Jacopo Celli 00046605
0000034288 see paper; … - - Familial, autosomal recessive - - - - - Jacopo Celli 00046606
0000034289 see paper; … - - Isolated (sporadic) - - - - - Jacopo Celli 00046607
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