Global Variome shared LOVD

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Phenotype #0000276514 Individual ID 00382665 Associated disease - Phenotype details see paper Diagnosis/Initial retinal disease Inheritance Familial, autosomal recessive Diagnosis/Definite Stargardt disease, type 1 (STGD1) Age/Examination - Age/Diagnosis 8y Age/Onset 6y Phenotype/Onset - Protein - Owner name Anna Tracewska Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-09-09 15:06:10 +02:00 (CEST) Date last edited N/A

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