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) - - 42 42 CDH23, CEACAM16, MYO15A, MYO6, MYO7A, OTOF, OTOG, PCDH15, TECTA, TMC1, USH1C - -
00350 DFNA deafness, nonsyndromic (DFNA, autosomal dominant) 124900 - 232 232 CEACAM16, DIAPH1, GRHL2, MYO6, MYO7A, TECTA, TMC1 - -
02580 DFNA-22 deafness, autosomal dominant, type 22 (DFNA-22) 606346 - 1 1 MYO6 - -
02707 DFNB-37 deafness, autosomal recessive, type 37 (DFNB-37) 607821 - 0 0 MYO6 - -
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