Global Variome shared LOVD

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Phenotype #0000333633 Individual ID 00444380 Associated disease ? Diagnosis/Initial anterior segment dysgenesis Diagnosis/Definite - Phenotype details see paper; ..., bilateral anterior segment dysgenesis; symptomatic mother early cataract with bilateral posterior embryotoxon Inheritance Familial Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Tumor/MSI - Diagnosis/Criteria - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2023-12-23 17:05:31 +01:00 (CET) Date last edited N/A

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