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 - -
06877 DFNA deafness, nonsyndromic (DFNA, autosomal dominant) - - 20 8 GREB1L, MYO6, MYO7A, REST, TECTA, TMC1 - -
02580 DFNA22 deafness, autosomal dominant, type 22 (DFNA-22) 606346 AD 2 2 MYO6 - -
02707 DFNB37 deafness, autosomal recessive, type 37 (DFNB-37) 607821 AR - - MYO6 - -
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