All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05458 DFN deafness, nonsyndromic (DFN) - - 48 43 CDH23, CEACAM16, FAM65B, MYO15A, MYO6, MYO7A, OTOF, OTOG, PCDH15, PDZD7, TECTA, TMC1, USH1C - -
00350 DFNA1 deafness, autosomal dominant, type 1 124900 AD 378 236 CEACAM16, DIAPH1, GRHL2, MYO6, MYO7A, TECTA, TMC1 - -
02596 DFNA36 deafness, autosomal dominant, type 36 (DFNA-36) 606705 AD 0 0 TMC1 - -
05400 DFNB deafness, autosomal recessive (DFNB) - - 871 870 CDH23, CIB2, FAM65B, MYO15A, MYO7A, OTOF, OTOG, PCDH15, S1PR2, STRC, TMC1, USH1C - autosomal recessive
02330 DFNB7 deafness, autosomal recessive, type 7 (DFNB-7) 600974 AR 8 8 TMC1 - -
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