Global Variome shared LOVD

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Phenotype #0000186424 Individual ID 00246573 Associated disease CSNB Phenotype details see paper; … Diagnosis/Initial incomplete congenital stationary night blindness Inheritance Familial, X-linked recessive Diagnosis/Definite CSNB-2A Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Christina Zeitz Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2019-07-12 19:10:49 +02:00 (CEST) Date last edited N/A

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