Global Variome shared LOVD

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Phenotype #0000354851 Individual ID 00469699 Associated disease ASGD2 Phenotype details see paper; ..., Peters anomaly, bilateral corneal opacities, developmental glaucoma, iris–retina coloboma (3/4), anterior segment dysgenesis, iridolenticular adhesions, nystagmus (3/4); no skeletal abnormalities, no physical disabilities, no cardiovascular diseases, no intellectual disability Diagnosis/Initial Peters anomaly 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 14:12:01 +01:00 (CET) Date last edited N/A

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