Global Variome shared LOVD

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Phenotype #0000291723 Individual ID 00398636 Associated disease - Phenotype details best corrected visual acuity: right eye, 20/125, left eye, 20/125, full-field photopic electroretinography right /left eye: a wave, b wave, flicker:nonrecordable/nonrecordable, nonrecordable/nonrecordable, nonrecordable/nonrecordable, optical coherence tomography: mild foveal atrophy without cavitation both eyes, fundus autofluorescence: focal foveal hyperfluoresence Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite achromatopsia Age/Examination 23y (23 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 2022-01-07 19:12:05 +01:00 (CET) Date last edited N/A

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