All diseases

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

ID     

AscendingAbbreviation     

Name     

OMIM ID     

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 - -