Global Variome shared LOVD

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Phenotype #0000270208 Individual ID 00374998 Associated disease - Phenotype details see paper; ..., foveal hypoplasia Diagnosis/Initial achromatopsia Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 17y (17 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2021-05-27 19:02:46 +02:00 (CEST) Date last edited N/A

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