Global Variome shared LOVD

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Phenotype #0000127805 Individual ID 00155306 Associated disease FECD Phenotype details see paper; … Diagnosis/Initial dystrophy, corneal, Fuchs endothelial (FECD) 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 2018-03-23 10:03:06 +01:00 (CET) Date last edited 2018-03-23 10:05:59 +01:00 (CET)

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