Global Variome shared LOVD

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Phenotype #0000300662 Individual ID 00408545 Associated disease - Phenotype details psychophysical and electroretinographic evidence of rod dysfunction greater than cone dysfunction; dark adaptometry: abnormalities with regional retinal variation in degree Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite Sorsby fundus dystrophy Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-04-22 16:00:18 +02:00 (CEST) Date last edited N/A

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