Global Variome shared LOVD

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Phenotype #0000331204 Individual ID 00441796 Associated disease CTRCT Phenotype details see paper; ..., bilateral congenital cataracts Diagnosis/Initial cataract Inheritance Familial, autosomal dominant Diagnosis/Definite CTRCT1 Age/Examination 05y (5 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 2023-11-12 20:31:57 +01:00 (CET) Date last edited N/A

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