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
01031 CAASDS craniofacial anomalies and anterior segment dysgenesis syndrome (CAASDS 614195 - - - VSX1 - -
05568 KCTN1 keratoconus, type 1 (KTCN-1) 148300 AD 7 7 VSX1 - -
01029 KTCN keratoconus (KTCN) - - 16 15 VSX1 - -
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