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
01720 - dystrophy, corneal, and perceptive deafness 217400 - - - SLC4A11 - -
01721 - dystrophy, corneal, endothelial, type 2 217700 - - - SLC4A11 - -
03296 FECD-4 dystrophy, corneal, Fuchs endothelial, type 4 (FECD-4) 613268 - - - SLC4A11 - -
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