Global Variome shared LOVD

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Phenotype #0000306365 Individual ID 00414566 Associated disease - Phenotype details refractive error: high myopia; best corrected visual acuity: not available; full field electroretinography, flicker: amplitude: 62, implicit time: 36.3; mixed amplitude: a-wave: 174, b-wave: 145; rod response: absent Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite congenital stationary night blindness Age/Examination 18y (18 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-07-29 12:13:59 +02:00 (CEST) Date last edited N/A

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