Global Variome shared LOVD

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Phenotype #0000355134 Individual ID 00469989 Associated disease ASGD Diagnosis/Initial anterior segment dysgenesis Diagnosis/Definite ASGD2 Phenotype details see paper; ..., congenital anterior segment dysgenesis, keratoconus, congenital bilateral corneal haze, microphthalmia Inheritance Familial, autosomal recessive Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2025-11-24 13:20:58 +01:00 (CET) Date last edited N/A

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