All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05458 DFN deafness, nonsyndromic (DFN) - - 49 44 CDC14A, CDH23, CEACAM16, FAM65B, MYO15A, MYO6, MYO7A, OTOF, OTOG, PCDH15, PDZD7, TECTA, TMC1, USH1C - -
00350 DFNA1 deafness, autosomal dominant, type 1 124900 AD 312 236 CEACAM16, DIAPH1, GRHL2 - -
03687 DFNA4B deafness, autosomal dominant, type 4b (DFNA-4B) 614614 AD - - CEACAM16 - -
06441 DFNB113 Deafness, autosomal recessive 113 618410 AR - - CEACAM16 - -
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