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
00655 BOR1 branchiootorenal syndrome, with/without cataract, type 1 (BOR-1) 113650 AD 1 1 EYA1, SIX1 - -
00989 BOS3 branchiootic syndrome, type 3 608389 AD - - SIX1 - -
00990 DFNA23 deafness, autosomal dominant, type 23 (DFNA-23) 605192 AD - - SIX1 - -
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