Global Variome shared LOVD

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Phenotype #0000127802 Individual ID 00155303 Associated disease FECD Phenotype details see paper; ..., fully penetrant Diagnosis/Initial dystrophy, corneal, Fuchs endothelial Inheritance Familial, autosomal dominant Diagnosis/Definite FECD-3 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 2018-03-23 09:22:30 +01:00 (CET) Date last edited N/A

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