Global Variome shared LOVD

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Phenotype #0000354855 Individual ID 00469703 Associated disease ASGD2 Phenotype details see paper; ..., bilateral microphthalmia, corneal opacity, anterior segment dysgenesis Diagnosis/Initial anterior segment dysgenesis Inheritance Familial, autosomal recessive Diagnosis/Definite ASGD2 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 2025-11-18 14:43:42 +01:00 (CET) Date last edited N/A

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