Global Variome shared LOVD

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Phenotype #0000055064 Individual ID 00075289 Associated disease STGD1 Phenotype details Stargardt disease; ophthalmoscopically characteristic retinal disorder, bilateral central vision loss, dark choroid Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 13y Phenotype/Onset visual impairment based on anamnestic medical records Protein - Owner name Stéphanie Cornelis Database submission license Creative Commons Attribution 4.0 International Created by Stéphanie Cornelis Date created 2016-02-22 12:22:09 +01:00 (CET) Date last edited N/A

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