Global Variome shared LOVD

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Phenotype #0000199384 Individual ID 00260852 Associated disease CTRCT Phenotype details see paper; ..., Diagnosis/Initial congenital cataract Inheritance Familial, autosomal recessive Diagnosis/Definite CTRCT-36 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 2019-08-09 08:50:03 +02:00 (CEST) Date last edited N/A

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