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
01180 ASGD1 dysgenesis, anterior segment, type 1 (ASGD1) 107250 - 2 2 FOXE3, PITX3 - -
02964 CTCRT11;CTPP4 cataract, type 11, multiple types (CTRCT-11, cataract, posterior polar, type 4 (CTPP-4)) 610623 AD;AR 5 5 PITX3 - -
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