Global Variome shared LOVD

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Phenotype #0000353434 Individual ID 00468282 Associated disease CTRCT Phenotype details see paper; ..., poor vision left eye since childhood; mother bilateral congenital cataracts Diagnosis/Initial poor vision Inheritance Familial, autosomal dominant Diagnosis/Definite CTRCT2 Age/Examination 30y (30 years) 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 2025-11-08 15:24:50 +01:00 (CET) Date last edited N/A

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