Phenotypes for disease #02283 (DFNB2 (deafness, autosomal recessive, type 2 (DFNB-2)), OMIM:600060)

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000046719 Congenital, severe HL - - Familial, autosomal recessive - - - - - Zippi Brownstein 00060231
0000046720 Congenital, moderate HL - - Familial, autosomal recessive - - - - - Zippi Brownstein 00060232
0000046724 di-genic inheritance; congenital, profound - - Complex - - - - - Zippi Brownstein 00060237
0000046725 Congenital profound HL - - Familial, autosomal recessive - - - - - Zippi Brownstein 00060238
0000046787 congenital, NSHL - - Familial, autosomal recessive - - - - - Johan den Dunnen 00060289
0000046788 congenital, NSHL - - Familial, autosomal recessive - - - - - Johan den Dunnen 00060290
0000046789 congenital, NSHL - - Familial, autosomal recessive - - - - - Johan den Dunnen 00060291
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