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
03297 FECD6 dystrophy, corneal, Fuchs endothelial, type 6 (FECD-6) 613270 - - - ZEB1 - -
05413 PPCD dystrophy, corneal, posterior polymorphous (PPCD) - - 42 42 COL8A2, GRHL2, OVOL2, ZEB1 - -
02825 PPCD3 dystrophy, corneal, posterior polymorphous, type 3 (PPCD-3) 609141 - 3 3 ZEB1 - -
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