Global Variome shared LOVD

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Phenotype #0000334388 Individual ID 00445135 Associated disease CTRCT Phenotype details see paper; ...,bilateral congenital cataract, amblyopia and nystagmus left eye; developmental milestones normal Diagnosis/Initial congenital cataract Inheritance Familial, autosomal dominant Diagnosis/Definite CTRCT3 Age/Examination 2y6m (2 years, 6 months) 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 2024-01-03 11:39:20 +01:00 (CET) Date last edited N/A

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