Global Variome shared LOVD

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Phenotype #0000298957 Individual ID 00406471 Associated disease - Phenotype details best corrected visual acuity right, left eye: 0.3/0.05, spherical refraction: 0.5/0.5, color vision: PD15 rat; unable to discriminate colors; nagel anomaloscope; protan defect, glare sensitivity: increased, night vision: normal Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite cone dystrophy Age/Examination 36y (36 years) Age/Diagnosis - Age/Onset <18y Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-03-31 09:55:29 +02:00 (CEST) Date last edited N/A

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