Global Variome shared LOVD

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Phenotype #0000039290 Individual ID 00052713 Associated disease RD Phenotype details retinal dystrophy, early-onset; macular degeneration, absence of normal pupil response, pigmentary changes over time, poor or loss in night vision, nystagmus Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Muhammad Ajmal Database submission license No license selected Created by Muhammad Ajmal Date created 2015-10-26 17:05:36 +01:00 (CET) Date last edited N/A

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