Global Variome shared LOVD

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Phenotype #0000303782 Individual ID 00411755 Associated disease - Phenotype details Night blindness; BCVA: RE -0.08/LE -0.08No clear scotoma Diagnosis/Initial occult macular dystrophy (OMD) Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 50y (50 years) Age/Diagnosis - Age/Onset 50y Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-06-18 03:05:08 +02:00 (CEST) Date last edited N/A

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