Global Variome shared LOVD

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Phenotype #0000306395 Individual ID 00414596 Associated disease - Phenotype details refractive error: -9.25; best corrected visual acuity: fix, follow and maintain; full field electroretinography, flicker: amplitude: 84, implicit time: 35; mixed amplitude: a-wave: WNL, b-wave: severely reduced; rod response: not available Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite congenital stationary night blindness Age/Examination 2y6m (2 years, 6 months) 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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