All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06877 DFNA deafness, nonsyndromic (DFNA, autosomal dominant) - - 20 8 DFNA5, GREB1L, MYO6, MYO7A, REST, TECTA, TMC1 - -
02333 DFNA5 deafness, autosomal dominant, type 5 (DFNA-5) 600994 AD 3 1 DFNA5 - -
04294 SNHL hearing loss, sensorineural (SNHL) - - 24 29 DFNA5 - -
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