Global Variome shared LOVD

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Phenotype #0000334171 Individual ID 00444921 Associated disease CTRCT Phenotype details see paper; ..., bilateral cataract, aphakic glaucoma, buphthalmos, scleromalacia; mother cataracts, brother cataracts, nonverbal/intellectual disability Diagnosis/Initial cataract Inheritance Familial, autosomal dominant Diagnosis/Definite - 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 2023-12-28 19:27:56 +01:00 (CET) Date last edited N/A

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