Global Variome shared LOVD

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Phenotype #0000308309 Individual ID 00416589 Associated disease - Phenotype details extremely poor vision Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite retinitis pigmentosa Age/Examination 60y (60 years) Age/Diagnosis - Age/Onset 20y Phenotype/Onset severe night blindness Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-09-05 15:54:25 +02:00 (CEST) Date last edited N/A

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