Global Variome shared LOVD

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Phenotype #0000308068 Individual ID 00416301 Associated disease - Phenotype details night vision deficiency since age 16 and loss of side vision in his 40; worse than in proband, vision gradually decreased to light perception in both eyes by age 54 Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite retinitis pigmentosa Age/Examination 54y (54 years) Age/Diagnosis - Age/Onset 16y Phenotype/Onset night vision deficiency Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-08-26 13:40:12 +02:00 (CEST) Date last edited N/A

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