Global Variome shared LOVD

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Phenotype #0000084378 Individual ID 00106573 Associated disease ROP Phenotype details retinopathy of prematurity (ROP) Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - 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 2010-06-06 16:39:21 +02:00 (CEST) Date last edited N/A

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