Global Variome shared LOVD

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Phenotype #0000299655 Individual ID 00407301 Associated disease - Phenotype details VAOD: 20/32 - VAOS: 20/40 Diagnosis/Initial autosomal dominant retinitis pigmentosa (adRP) Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 16y (16 years) Age/Diagnosis - Age/Onset - Phenotype/Onset early childhood night blindness Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-04-06 13:32:24 +02:00 (CEST) Date last edited N/A

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