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
05645 AAT11 aneurysm, aortic, thoracic, familial, type 11 (AAT11) 617349 AD 1 1 FOXE3 - -
02923 ASGD2 dysgenesis, anterior segment, type 2 610256 AR 16 16 FOXE3 - -
05644 CTRCT34 cataract, multiple types, type 34 (CTRCT-34) 612968 - - - FOXE3 - -
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