Global Variome shared LOVD

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Phenotype #0000028731 Individual ID 00038188 Associated disease - Phenotype details Night blindness, peripheral RPE changes with bone spicules, perifoveal atrophy, pale optic disc, narrowing of retinal vessels Diagnosis/Initial retinitis pigmentosa Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset 25y Phenotype/Onset ? Protein - Owner name Frans Cremers Database submission license Creative Commons Attribution 4.0 International Created by Frans Cremers Date created 2015-05-01 22:00:00 +02:00 (CEST) Date last edited 2020-08-25 10:48:31 +02:00 (CEST)

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