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 CDPD dystrophy, corneal, endothelial, and perceptive deafness 217400 AR - - SLC4A11 - -
01721 CHED dystrophy, corneal, endothelial 217700 AR 46 16 SLC4A11 - autosomal recessive
03296 FECD4 dystrophy, corneal, Fuchs endothelial, type 4 613268 - - - SLC4A11 - -
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