Global Variome shared LOVD

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Phenotype #0000317902 Individual ID 00426748 Associated disease - Phenotype details BCVA:s 0.4 with -5.75 to 3.5160 OD and 0.4 with -5.25 to 3.0180 OS Diagnosis/Initial autosomal dominant retinitis pigmentosa (adRP) Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 19y (19 years) Age/Diagnosis - Age/Onset 7y Phenotype/Onset poor night vision Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-12-02 14:17:29 +01:00 (CET) Date last edited N/A

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