Global Variome shared LOVD

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Phenotype #0000317905 Individual ID 00426751 Associated disease - Phenotype details VA: OD:0.4/OS:0.3; absent ; migration of retinal pigment epithelium in mid periphery Diagnosis/Initial autosomal dominant retinitis pigmentosa (adRP) Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 27y (27 years) Age/Diagnosis - Age/Onset <3y Phenotype/Onset night blindness 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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