All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02487 ASGD5 dysgenesis, anterior segment, type 5, multiple subtypes 604229 AD 5 5 CYP1B1, PAX6, PITX2 - -
06466 ASGD6 Anterior segment dysgenesis 6, multiple subtypes 617315 - - - CYP1B1 - -
01814 GLC3A glaucoma, congenital, primary, type 3A (GLC-3A) 231300 AR 45 45 CYP1B1 - -
02331 GLC3B glaucoma, congenital, primary infantile, type 3B (GLC-3B) 600975 - 1 1 CYP1B1, LTBP2 - -
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