Global Variome shared LOVD

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Phenotype #0000028685 Individual ID 00038142 Associated disease RD Phenotype details early-onset retinal dystrophy, bilateral visual loss before the age of 6 months, nystagmus, undetectable or significantly reduced ERG Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 1y Phenotype/Onset ? Protein - Owner name Frans Cremers Database submission license Creative Commons Attribution 4.0 International Created by Frans Cremers Date created 2015-05-01 22:00:00 +02:00 (CEST) Date last edited N/A

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