Global Variome shared LOVD

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Phenotype #0000353679 Individual ID 00468527 Associated disease CTRCT Phenotype details aniridia, corneal limbal insufficiency, nystagmus, severe axile myopia, mild lens opacities, fibrous posterior capsular reaction after lens surgery Diagnosis/Initial congenital cataract Inheritance Unknown Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2025-11-10 14:21:08 +01:00 (CET) Date last edited N/A

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