All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04336 FECD-3 dystrophy, corneal, Fuchs endothelial, type 3 (FECD-3) 613267 - 0 0 TCF4 - -
00742 PTHS Pitt-Hopkins syndrome (PTHS) 610954 - 109 109 TCF4 - -
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