Phenotypes for disease #02330 (DFNB7 (deafness, autosomal recessive, type 7 (DFNB-7)), OMIM:600974)

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     
0000045634 congenital, profound hearing loss - - Familial, autosomal recessive - - - - - Zippi Brownstein 00059045
0000045635 congenital, profound hearing loss - - Familial, autosomal recessive - - - - - Zippi Brownstein 00059046
0000045636 congenital, profound hearing loss - - Familial, autosomal recessive - - - - - Zippi Brownstein 00059047
0000046728 Congenital, profound NSHL - - Familial, autosomal recessive - - - - - Zippi Brownstein 00060243
0000046729 Congenital, profound NSHL - - Familial, autosomal recessive - - - - - Zippi Brownstein 00060244
0000046742 Congenital, profound NSHL - - Familial, autosomal recessive - - - - - Zippi Brownstein 00060253
0000046743 Congenital, profound NSHL - - Familial, autosomal recessive - - - - - Zippi Brownstein 00060254
0000277068 bilateral symmetric severe group one hearing loss - - Familial, autosomal recessive - 03y - - - David Baux 00383282
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