Global Variome shared LOVD

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Phenotype #0000299630 Individual ID 00407276 Associated disease - Phenotype details field loss at 18y, bone-spicule pigment +/+ Diagnosis/Initial autosomal dominant retinitis pigmentosa (adRP) Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 25y (25 years) Age/Diagnosis - Age/Onset 14y Phenotype/Onset 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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