Global Variome shared LOVD

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Phenotype #0000144056 Individual ID 00183319 Associated disease CTRCT Phenotype details see paper; ..., infantile or early-childhood cataracts and visual impairment Diagnosis/Initial infantile cataract Inheritance Familial, autosomal recessive 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 2018-10-22 18:45:27 +02:00 (CEST) Date last edited N/A

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