Global Variome shared LOVD

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Phenotype #0000335774 Individual ID 00446572 Associated disease CTRCT Phenotype details see paper; ..., congenital cataract, iris coloboma (3/4) Diagnosis/Initial congenital cataract Inheritance Familial, autosomal dominant Diagnosis/Definite CTRCT4 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 2024-01-18 09:13:36 +01:00 (CET) Date last edited N/A

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