Phenotypes for disease #04622 (DFNX2 (deafness, X-linked, type 2 (DFNX-2)), OMIM:304400)

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     
0000046752 - - - Familial, X-linked recessive - - - Congenital - Zippi Brownstein 00060263
0000090303 DFNX2; Hearing_loss - - Isolated (sporadic) - - - - - Thomas Parzefall 00114821
0000090304 DFNX2; Hearing_loss - - Familial, X-linked recessive - - - - - Thomas Parzefall 00114822
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