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