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) - - 50 45 CDC14A, CDH23, CEACAM16, FAM65B, MYO15A, MYO6, MYO7A, OTOF, OTOG, PCDH15, PDZD7, TECTA, TMC1, USH1C - -
06877 DFNA deafness, nonsyndromic (DFNA, autosomal dominant) - - 20 8 GREB1L, MYO6, MYO7A, REST, TECTA, TMC1 - -
02370 DFNA12 deafness, autosomal dominant, type 12 (DFNA-12) 601543 AD 3 3 TECTA - -
02462 DFNB21 deafness, autosomal recessive, type 21 (DFNB-21) 603629 AR 1 1 TECTA - -
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