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
01338 FECD1 dystrophy, corneal, Fuchs endothelial, type 1 (FECD-1) 136800 AD 19 6 COL8A2 - -
05413 PPCD dystrophy, corneal, posterior polymorphous (PPCD) - - 42 42 COL8A2, GRHL2, OVOL2, ZEB1 - -
02824 PPCD2 dystrophy, corneal, posterior polymorphous, type 2 (PPCD-2) 609140 AD - - COL8A2 - autosomal dominant
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